Next Article in Journal
Dual-Fluoroscopy vs. Single-Fluoroscopy in Balloon Kyphoplasty: A Study of Efficiency and Safety
Previous Article in Journal
Prothrombotic Rebound After Discontinuation of Direct Oral Anticoagulants Therapy: A Systematic Review
Previous Article in Special Issue
The Effect of Exercise Program Interventions on Frailty, Clinical Outcomes, and Biomarkers in Older Adults: A Systematic Review
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Effects of an 8-Month Multicomponent Training Program in Body Composition, Functional Fitness, and Sleep Quality in Aged People: A Randomized Controlled Trial

by
Pedro Forte
1,2,3,4,*,
Samuel G. Encarnação
2,3,5,
Luís Branquinho
6,7,8,
Tiago M. Barbosa
3,4,
António M. Monteiro
3,4 and
Daniel Pecos-Martín
1
1
Physiotherapy and Pain Group, Department of Physical Therapy, University of Alcala, 28801 Madrid, Spain
2
Department of Sports, Higher Institute of Educational Sciences of the Douro, 4560-708 Penafiel, Portugal
3
Research Centre for Active Living and Wellbeing (LiveWell), Instituto Politécnico de Bragança, 5300-253 Bragança, Portugal
4
Department of Sports Sciences, Instituto Politécnico de Bragança, 5300-253 Bragança, Portugal
5
Department of Physical Activity and Sport Sciences, Universidad Autónoma de Madrid (UAM), 28049 Madrid, Spain
6
Biosciences Higher School of Elvas, Polytechnic Institute of Portalegre, 7350-092 Portalegre, Portugal
7
Life Quality Research Centre (LORQ-CIEQV), 2001-964 Santarém, Portugal
8
Research Center in Sport Sciences, Health Sciences and Human Development (CIDESD), 6201-001 Covilhã, Portugal
*
Author to whom correspondence should be addressed.
J. Clin. Med. 2024, 13(21), 6603; https://doi.org/10.3390/jcm13216603
Submission received: 20 September 2024 / Revised: 21 October 2024 / Accepted: 1 November 2024 / Published: 3 November 2024

Abstract

:
Background/Objectives: This study examined the effects of an intervention on anthropometrics, body composition, physical fitness, and sleep quality in aged individuals, comparing a control group (N = 11) and an experimental group (N = 13) across two measurement points. Methods: A multicomponent training program of 8 months was adopted as the intervention group. A bioimpedance balance, functional fitness test, and Pittsburgh Sleep Quality Index measured body composition, functional fitness, and sleep quality. Results: Both groups showed minimal changes in body mass and hand grip strength. However, the experimental group experienced significant improvements in physical fitness, including a 26% increase in arm curl repetitions, an 18% reduction in 5 times sit-to-stand (5TSTS) completion time, and a 29% rise in 2-min step test (2MST) steps, indicating enhanced muscle endurance and cardiovascular fitness. Flexibility decreased significantly in the experimental group, while body fat percentage was reduced by 10%. Sleep quality improved by 47% in the experimental group but declined by 14% in the control group. Correlational analysis revealed that better sleep quality was linked to improved fitness performance and reduced body fat in the experimental group, with post-intervention results further confirming the connection between sleep and fat reduction. In the control group, improved sleep quality was associated with higher metabolic rates after 8 months. Conclusions: These findings suggest that the intervention positively impacted physical fitness and sleep quality, with potential benefits for overall health.

1. Introduction

The elderly commonly experience deterioration in the visual and proprioceptive systems, which can impact balance and postural control [1,2]. In older adults, proprioceptive information plays an important role in maintaining balance. Other studies [3,4] have underscored the role of balance training in improving proprioception and dynamic balance. The balance training type can enhance ankle stability (i.e., lower limbs function), neuromuscular function (i.e., related to strength), and postural control system efficiency [5,6]. This highlights the significance of incorporating balance exercises targeting proprioception in older adults to enhance dynamic balance and reduce the risk of falls [7]. Finally, [8] identified a link between sleep quality and dynamic balance, indicating that poor sleep quality may be associated with dynamic imbalance in older adults. However, the authors were unable to evaluate the effects of training exercise programs on physical fitness, sleep quality, and balance.
The relationship between sleep quality and physical exercise in older people has been widely documented in the literature. Studies have shown that aerobic exercise can improve self-reported sleep and quality of life in older adults with insomnia [9]. Additionally, systematic reviews have indicated that physical activity programs positively impact various aspects of sleep in generally healthy older adults [10]. A study [11] showed that in community-dwelling older adults, exercise can impact sleep through mechanisms such as light exposure, temperature regulation, and mood. A recent systematic review and meta-analysis have further supported the positive effects of physical exercise programs on improving sleep quality in older adults [12]. However, a longitudinal study demonstrated that sleep quality plays a crucial role in older adults’ level of physical activity, with better sleep quality promoting more physical activity [13]. Older individuals often struggle with changing positions during sleep due to musculoskeletal pain, decreased mobility, and motor impairments [14,15], leading to discomfort and sleep disturbances [16]. Also, chronic pain conditions and limited ability to change positions worsen sleep difficulties [17], compounded by physical disabilities and cognitive impairments [15]. Poor sleep quality is independently linked to physical disability and functional limitations in older adults [18,19], stressing the need to address sleep disturbances to enhance overall health and well-being [18,20]. Upon that, physical exercise training programs may improve body functionality and possibly sleep quality. Between the different exercise training programs, the American College of Sports Medicine (ACSM) previously highlighted the importance of multicomponent training (MCT) for older adults, citing its benefits for strength, aerobic fitness, and balance [21]. This type of program (MCT) including exercises for aerobics, resistance, balance, and flexibility composes the multicomponent training [22,23]. It could improve metabolic outcomes, functional and cognitive performance, cardiorespiratory fitness and autonomy. The fundamental part of each training session aims to train aerobic, resistance, and balance skills [22,23]. Subsequent research has supported these claims. A review of 27 studies showed that MCT improves physical fitness and overall health in older populations [24]. Additionally, a meta-analysis comparing aerobic training, resistance training, and MCT found MCT to be the most effective for cognitive improvement [25]. Recent research also supports MCT’s positive effects on attention and executive function in older adults [26]. MCT programs include exercises targeting physical and cognitive health [5,27,28], aiming to enhance muscle mass, power output, functional outcomes, cognitive function, and brain health [6,29]. Overall, MCT appears effective in improving physical function, muscle mass, cognitive function, and mental health in older adults, even those with conditions like mild cognitive impairment, dementia, Alzheimer’s disease, and sarcopenia [28,30].
The relationship between exercise, physical fitness, body composition, and sleep quality in older adults may be complex and interconnected [31,32]. In light of the above, it seems important to continue investigating to understand the complexity of the phenomenon to broadly understand the effects of exercise on sleep quality and its associations with physical fitness and body composition, which can play a fundamental role in the development of interventions that promote healthy aging and improve the well-being of older individuals. Given this, this research aimed to evaluate the effects of 8 months of multicomponent training programs on critical variables such as physical fitness, body composition, and sleep quality. Additionally, we aim to seek the associations between physical fitness, body composition, and sleep quality. It was hypothesized that an 8-month multicomponent training program would significantly positively affect physical fitness, body composition, and sleep quality.

2. Materials and Methods

2.1. Design and Sample

This was a randomized controlled trial with pre- and post-intervention measurements (The trial was registered with the ID NCT06646380 on the ClinicalTrials.gov: https://clinicaltrials.gov/study/NCT06646380). Forty participants were contacted to participate in this study and randomly divided into two groups of 20 participants (Control and Experimental Groups). The convenience sample’s mean age was 69 years old. The sample was recruited in the Bragança Municipality in Portugal. All participants were aged community people. All procedures were carried out in accordance with the recommendations of the Declaration of Helsinki for human studies. The research project received approval by the Ethical Committee of the Instituto Politécnico de Bragança (number: 2576). The participants were instructed to maintain normal daily activities to prevent physical inactivity. The participants were asked to complete a sample characterization questionnaire during the first visit. The criteria for inclusion in the study were: (i) being aged 65 years or older, (ii) maintaining functional independence in daily tasks, (iii) having no severe chronic diseases or medications to sleep that could affect the results, (iv) do not have significant cardiovascular, muscular, metabolic, or joint complications. Among the 40 contacted participants, only 32 subjects completed the first evaluation (15 were from the experimental group (EG) and 17 were from the control group (CG)). Eight participants (25% of the total sample) dropped out due to undeclared health issues and losing interest in the study. Between them, 2 participants from the experimental group did not attend the minimum of 75% of the exercise sessions. Thus, the data from the remaining participants (13 in EG: 11 women and 2 men) were not involved in any physical exercise or similar intervention during all follow-ups. The CG (11: 9 women and 2 men) were instructed to maintain daily routines. However, the typical profile of this group was that the participants were regularly physically active people. Most participate in municipal activities like nature walking, physical activity sessions including dance (casually), board and card games, and traditional games (Bocce, Adapted Bowling, and darts). After 32 weeks and in the second moment, only 24 participants finalized the study (13 from EG and 11 from CG). Figure 1 depicts the sampling flowchart of the sampling process.

2.2. Intervention Program

The exercise program integrated aerobic, resistance, flexibility, and balance activities [22,23]. Each session lasted between 50 and 60 min and consisted of five key components (Figure 2): (i) a 5–8 min warm-up with slow walking and stretching; (ii) 15–20 min of aerobic activities, including walking, jogging, aerobics, and dancing, with at least 8–10 min; and (iii) 1–3 sets of resistance exercises using elastic bands and free weights in a circuit format, targeting major muscle groups, such as knee flexors/extensors, shoulder abductors/adductors, elbow flexors/extensors, pectorals, and abdominals, with 40–60 s of rest between sets. To ensure proper familiarization and technique, the training intensity started lower at the beginning of each month, beginning with 8 repetitions in 1 set and gradually increasing to 12–15 repetitions and 3 sets; (iv) 5–8 min of static and dynamic balance training using sticks, balls, and balloons; and (v) a 5-min cool-down period at the end of each session, including breathing exercises and stretching.
The repetitions and time increased by 30% after each 2-month intervention. The training intensity was controlled using Borg’s 10-point categoric ratio scale (CR-10) [33]. The coaches aimed to work in an intensity range from 3 (moderate) to 5 (intense). Table 1 presents the training session plan.

2.3. Anthropometrics and Body Composition

Anthropometric measurements included height and weight. Body composition was assessed using a digital bioimpedance scale (Tanita BC-50, IL, USA), which recorded variables such as lean mass, body fat percentage, bone mineral density, visceral fat, total body mass, muscle mass, fat mass, and bone density. Evaluations were conducted in the morning before breakfast, with participants wearing only light clothing and no shoes or socks. Height was measured while the participants stood with their head aligned in the Frankfurt plane. Waist and hip circumferences were also measured. Metabolic variables, including systolic and diastolic blood pressure and resting heart rate, were recorded using an OMRON (M2 HEM-7143-E) and brachial cuff (Easy 22–32) (Amsterdam, The Netherlands). The metabolic rate was assessed via bioimpedance using the Tanita scale.

2.4. Physical Fitness

Handgrip strength was assessed using a digital palmar dynamometer (CAMRY®, Lisbon, Portugal), with the maximum kilograms-force (kgf) achieved using a palm grip as the measurement. The participants stood with their arms away from their body and, upon the researcher’s signal, exerted maximum palm grip force on the dynamometer for 4 s [34]. Each participant was given three attempts, and the highest recorded result was noted by the evaluator.
The Functional Fitness Test was used to assess the main physical parameters associated with functional mobility. The Functional Fitness Test evaluated key aspects of physical mobility [35]. It included the 2-Minute Step Test, where the evaluator set a knee height marker using a measuring tape to measure from the kneecap to the iliac crest, and participants aimed to take as many steps as possible in 2 minutes, with performance checks at 60 and 90 s. The Seat-to-Stand Test required participants to repeatedly sit and stand from a 43-cm highchair for 30 s, with the number of repetitions recorded. In the Arm Curl Test, participants seated on a 43-cm chair used a 2-kg dumbbell to perform elbow curls for 30 s. The Time-Up-and-Go Test involved starting from a seated position on a 43-cm chair, walking quickly around a cone placed 2.44 m away, and returning to the chair, with the time recorded after 2 attempts. The Sit and Reach Test, conducted while seated on a 43-cm chair with one leg extended and toes reached, and the Back Scratch Test, where participants attempted to touch one hand with the other behind their back, were timed in seconds.
The lower limb muscle power was assessed using the five-time sit-to-stand test with a chair 0.49 m high. The evaluator started the stopwatch when the participant stood up and stopped it after completing five repetitions, marking the time as soon as they sat back down for the fifth time. The evaluator encouraged the participant to maintain maximum speed and proper technique throughout the test. Each participant performed 2 attempts, with a 60-s rest between them, and the shortest time was recorded [36].

2.5. Sleep Quality

Sleep quality was assessed using the Pittsburgh Sleep Quality Index (PSQI), a 19-item questionnaire developed by Buysse et al. [37] and validated for the Portuguese population [38]. The PSQI items are divided into the following components: (1) subjective sleep quality, (2) sleep latency, (3) sleep duration, (4) habitual sleep efficiency, (5) sleep disturbances, (6) use of sleeping medication, and (7) daytime dysfunction. Each item is scored from 0 to 3, with the total score ranging from 0 to 21; higher scores indicate more severe sleep disturbances. A global score of 5 or higher in 2 components signifies significant sleep difficulties, while a score in 3 or more components indicates moderate sleep issues. A total score below 5 indicates good sleep quality, whereas a score above 5 indicates poor sleep quality.

2.6. Statistical Analysis

The analysis of the sample statistical power was classified as reduced of the prior recruited sample in this study (<0.80). The standard statistical methods were used to calculate the means and standard deviation. The Kolmogorov–Smirnov test allowed us to assess the normality of the distribution, and Levene’s test assessed the homogeneity (N < 30).
The t-test permitted the comparison of variables by sex and sleep quality, and Pearson’s correlation permitted the test of the association between the variables for the control and the experimental group, respectively. The test was made at a significance level of 5%. Effect sizes were calculated based on Cohen’s d and classified as 0.2—trivial; 0.6—small; 1.2—large; and>2.0—very large [39]. Statistical analyses were performed with 95% CI; p < 0.05. All procedures were performed with SPSS version 24.0 (SPSS, Inc., Chicago, IL, USA). Additionally, we applied statistical procedures based on Bayesian assumptions. For this purpose, a two-way mixed effect Bayesian ANOVA was applied to capture effects within, between, and interactions between within subjects [40]. This version of the classification analysis of variance is robust when statistical assumptions, such as minimal sample size and statistical power, are not satisfied [41]. For this purpose, we considered the main metric of significance, which is the Bayes factor, considering Jeffreys’s [42] cut-offs (≤3 = Anecdotal evidence, between 3 and 10 = Moderate evidence, >10 = Strong evidence). Thus, we considered only differences classified with a strong level of evidence to reject the null hypothesis in a 95% confidence interval [41,42]. The Bayesian ANOVA was performed in R, the statistical computing programming language (version 4.4.2.) [43].

3. Results

Table 2 shows the means, standard deviations (mean ± Sd), and percentage of variations for the control (N = 11) and experimental group (N = 13) across two measurement times (M1 and M2) anthropometrics and body composition, physical fitness, and sleep quality. Additionally, it presents the comparisons between moments for the control and experimental groups. In the control group, significant differences were only noted for total sleep (t = 2.869; p = 0.017; d = −0.865), indicating a statistically significant decrease in quality. In the experimental group, several variables showed significant differences. The Arm Curl exhibited a significant improvement (t = −4.696; p = 0.001; d = −0.373) in the number of arm curls performed. The 5TSTS showed a significant decrease in the time to perform five sit-to-stand movements (t = 5.392; p < 0.001; d = −0.058). CS30 had a significant (t = −8.469; p < 0.001; d = −0.161) decrease in the number of chair stands performed in 30 s. TUG showed a significant increase in the time to complete the test (t = 4.212; p = 0.001; d = 0.243). The Seat and Reach test revealed a decrease in flexibility (t = −4.127; p = 0.001; d = −0.265), and the Back Stretch test showed the same tendency (t = −3.722; p = 0.003; d = −0.519). The 2MST variable significantly increased the number of steps performed in two minutes (t = −9.617; p < 0.001; d = −0.040). The Total Fat (%) significantly decreased (t = 2.225; p = 0.046; d = 0.228), and lastly, the Sleep quality score significantly improved (t = 2.856; p = 0.014; d = −0.865).
Table 3 below presents the group comparison results after 32 weeks of multicomponent training intervention. The mixed effects Bayesian ANOVA revealed that there were only significant post-prior probabilities (p < 0.05) regarding increases in upper limb strength for the experimental group, with a significant isolated effect of time (Bayes Factor = 85.02357 ± 1.12%) and a significant group × time interaction (Bayes Factor = 80.38867 ± 1.76%). There was also a significant increase (p < 0.05) in the lower limb flexibility in favour of the experimental group, with only a group × time interaction (Bayes Factor = 7.937376 ± 2.16%). Finally, there was a significant increase in the absolute sleep scores regarding the control group, with a significant group × time interaction (Bayes Factor = 10.34395 ± 2.07%) highlighting the increased risk of sleep disorders in this group.
Intending to understand the link between physical fitness, body composition, and sleep quality, the Pearson correlation test presents significant associations with total sleep (Table 4). The control group revealed significant associations between total sleep quality and body water (Moment 2: r = 0.665; p = 0.026). The experimental group revealed significant associations between sleep quality TUG (Moment 1: r = 0.575; p = 0.040), total fat (Moment 1: r = 0.526; p = 0.046), Fat percentage (Moment 1: r = 0.619; p = 0.024 | Moment 2: r = 0.620; p = 0.024), and body water (Moment 1: r = 0.646; p = 0.017). Figure 3 presents the correlation heatmap.

4. Discussion

This study aimed to assess the effects of 8 months of multicomponent training programs on critical variables such as physical fitness, body composition, and sleep quality. It was hypothesized that a multicomponent training program of 8 months significantly improves physical fitness, body composition, and quality of life. The results revealed that after the multicomponent training program, the experimental group improved the arm curl, 5TSTS, CS30, 2MST, total fat (%), and sleep quality; conversely, the TUG, Seat and Reach, and the Back Stretch tests revealed worse results. The control group revealed a worse sleep quality after the follow-up.
Regarding the physical fitness variables, the improvements align with the literature, where multicomponent training programs improve physical fitness and functionality [22,24,30,44,45]. In the current research, the experimental group improved the variables related to aerobic and resistance exercise (arm curl, 5TSTS, CS30, 2MST). The lack of specificity of multicomponent training may explain these results. A previous study [33] revealed that, independent of the training type (multicomponent, resistance, or power), it was possible to note improvements in upper and lower limb strength, upper and lower limb flexibility and aerobic resistance but not in the TUG test after eight months of intervention. Also, after 8 months, a multicomponent training program improved the maximal voluntary contraction of upper and lower limbs in older women [46]. Another study [47] revealed that after 6 months of intervention, the Chair stand test, Arm curl, Chair sit and reach, Back scratch, TUG, 2MST, Hand grip strength, and BMI significantly improved. Regarding the body composition, the EG of the present study reduced the total fat percentage. This aligns with previous studies that applied a multicomponent training program in the older population, where fat mass was reduced after 8 [22] and 6 months [47]. However, there are quite controversial results at 6 months, where in some studies, total fat mass did not reduce after the intervention [46,48]. Furthermore, the multicomponent training programs seem to be adequate to improve aged people’s (>60 years old) physical fitness and frailty [49].
As for the sleep quality, the EG significantly improved the sleep quality. A systematic review with meta-analysis [12] revealed that exercise programs improved sleep quality. The same was noted when applying for multicomponent training programs. In the study by Vaz Fragoso et al. [46], in-home- and center-based participants from 24–30 months with moderate intensity and 5 times per week found sleep quality improvements in the participants. The study from Laredo-Aguilera et al. [50], with 10 weeks of duration and a self-determined intensity to perform 8–12 repetitions, 3 times per week, revealed significant improvements in sleep quality. Finally, Bademli et al. [51], in nursing home residents, applied a 20-week program with moderate intensity and 3–4 times per week and showed improved sleep quality scores. The studies are in line with the current study, where the multicomponent training program with 8-months duration and moderate intensity also improved sleep quality.
The present study evaluated associations between sleep quality, physical fitness, and body composition variables to understand the variables that may explain the total sleep quality for the CG and EG after and before the multicomponent training program. The CG revealed significant associations between total sleep quality and body water (Moment 2: r = 0.665; p = 0.026). The association between total sleep quality and body water was noted in the second evaluation moment and revealed that the higher the percentage of body water, the lower the sleep quality. During the night, many elderlies experience the need for frequent urination due to the difficulty of controlling it with aging [52,53,54]. With this need to frequently urinate, the circadian rhythm will negatively impact sleep continuity and quality [54,55]. The EG presented significant associations between sleep quality and TUG (baseline), total fat (baseline), and body water (baseline). The fat percentage presented significant associations with sleep quality at baseline and post-intervention). The results showed that before the multicomponent exercise program, the higher the TUG, the poorer the sleep quality. As for body composition, higher total fat and body water scores also indicate poor sleep quality. Factors such as waist circumference, visceral fat, and total fat can affect sleep quality through hormonal regulation, inflammation, and metabolic health [56,57], possibly affecting the circadian rhythm [54,55] and sleep quality.
Altogether, this study presents promising results regarding the effectiveness of exercise-based interventions to improve physical fitness and sleep quality. However, there are some important limitations to be addressed: (i) the sample of this study is too small and makes it impossible to perform sex comparisons or generalize the results; (ii) the intervention program lasted for 8 months, and daily life activities were not controlled; (iii) co-variates such as mental health or wellbeing behaviors were not assessed; (iv) only two time measures (before and after) were made in this study. Upon that, future research should be conducted: (i) higher sample sizes will allow generalizing of the results; (ii) monitoring daily life physical activity; (iii) mental health and well-being lifestyle should be assessed; (iv) different durations and types of exercise-based programs should be assessed.

5. Conclusions

The findings of this study demonstrate that a targeted physical fitness intervention can significantly improve physical performance and sleep quality in aging adults. The experimental group showed marked improvements in muscle endurance, as evidenced by increased arm curl repetitions and improved performance in the 5TSTS and 2MST tests. Additionally, the intervention led to a significant reduction in total fat percentage and enhanced sleep quality. In contrast, the control group exhibited a decline in sleep quality over the study period, highlighting the potential protective effects of physical exercise on sleep in older adults. These results underscore the importance of incorporating regular, targeted exercise programs into the routines of aging individuals to enhance overall health, physical fitness, and sleep quality.

Author Contributions

Conceptualization, P.F. and A.M.M.; methodology, A.M.M.; software, S.G.E.; validation, D.P.-M., L.B., and T.M.B.; formal analysis, P.F.; investigation, P.F. and S.G.E.; resources, A.M.M.; data curation, L.B.; writing—original draft preparation, P.F.; writing—review and editing, S.G.E., L.B., A.M.M., T.M.B., and D.P.-M.; visualization, S.G.E.; supervision, A.M.M., T.M.B., and D.P.-M.; project administration, A.M.M.; funding acquisition, T.M.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Research Center for Active Living and Wellbeing.

Institutional Review Board Statement

All procedures were carried out in accordance with the recommendations of the Declaration of Helsinki for human studies. The research project received approval by the Ethical Committee of the Instituto Politécnico de Bragança (number: 2576).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study. Written informed consent has been obtained from the patient(s) to publish this paper.

Data Availability Statement

Contact corresponding author.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Pasma, J.H.; Engelhart, D.; Maier, A.B.; Schouten, A.C.; van der Kooij, H.; Meskers, C.G.M. Changes in Sensory Reweighting of Proprioceptive Information during Standing Balance with Age and Disease. J. Neurophysiol. 2015, 114, 3220–3233. [Google Scholar] [CrossRef] [PubMed]
  2. Martellucci, S.; Pagliuca, G.; de Vincentiis, M.; Greco, A.; De Virgilio, A.; Nobili Benedetti, F.M.; Gallipoli, C.; Rosato, C.; Clemenzi, V.; Gallo, A. Features of Residual Dizziness after Canalith Repositioning Procedures for Benign Paroxysmal Positional Vertigo. Otolaryngol. Neck Surg. 2016, 154, 693–701. [Google Scholar] [CrossRef] [PubMed]
  3. Zhou, L.; Gong, W.; Wang, S.; Guo, Z.; Liu, M.; Chuang, S.; Bao, D.; Zhou, J. Combined Balance and Plyometric Training Enhances Knee Function, but Not Proprioception of Elite Male Badminton Players: A Pilot Randomized Controlled Study. Front. Psychol. 2022, 13, 947877. [Google Scholar] [CrossRef] [PubMed]
  4. Soares, N.M.M.; Dantas, E.H.M.; da Silva-Grigoletto, M.E.; dos Santos Silva, R.J.; Aidar, F.J.M.; da Silva Júnior, W.M.; Cabral, B.T.; Carneiro, A.L.; Garrido, N.D.; Reis, V.M. CIAFIS—Congresso Internacional de Atividade Física, Nutrição e Saúde. Motricidade 2018, 13, 1–200. [Google Scholar] [CrossRef]
  5. Suzuki, T.; Shimada, H.; Makizako, H.; Doi, T.; Yoshida, D.; Tsutsumimoto, K.; Anan, Y.; Uemura, K.; Lee, S.; Park, H. Effects of Multicomponent Exercise on Cognitive Function in Older Adults with Amnestic Mild Cognitive Impairment: A Randomized Controlled Trial. BMC Neurol. 2012, 12, 128. [Google Scholar] [CrossRef]
  6. de Bruin, E.; Eggenberger, P.; Schumacher, V.; Angst, M.; Theill, N. Does Multicomponent Physical Exercise with Simultaneous Cognitive Training Boost Cognitive Performance in Older Adults? A 6-Month Randomized Controlled Trial with a 1-Year Follow-Up. Clin. Interv. Aging 2015, 2015, 1335–1349. [Google Scholar] [CrossRef]
  7. Espejo-Antúnez, L.; Pérez-Mármol, J.M.; de los Ángeles Cardero-Durán, M.; Toledo-Marhuenda, J.V.; Albornoz-Cabello, M. The Effect of Proprioceptive Exercises on Balance and Physical Function in Institutionalized Older Adults: A Randomized Controlled Trial. Arch. Phys. Med. Rehabil. 2020, 101, 1780–1788. [Google Scholar] [CrossRef]
  8. Serrano-Checa, R.; Hita-Contreras, F.; Jiménez-García, J.D.; Achalandabaso-Ochoa, A.; Aibar-Almazán, A.; Martínez-Amat, A. Sleep Quality, Anxiety, and Depression Are Associated with Fall Risk Factors in Older Women. Int. J. Environ. Res. Public Health 2020, 17, 4043. [Google Scholar] [CrossRef]
  9. Reid, K.J.; Baron, K.G.; Lu, B.; Naylor, E.; Wolfe, L.; Zee, P.C. Aerobic Exercise Improves Self-Reported Sleep and Quality of Life in Older Adults with Insomnia. Sleep Med. 2010, 11, 934–940. [Google Scholar] [CrossRef]
  10. Vanderlinden, J.; Boen, F.; van Uffelen, J.G.Z. Effects of Physical Activity Programs on Sleep Outcomes in Older Adults: A Systematic Review. Int. J. Behav. Nutr. Phys. Act. 2020, 17, 11. [Google Scholar] [CrossRef]
  11. Dzierzewski, J.M.; Buman, M.P.; Giacobbi, P.R.; Roberts, B.L.; Aiken-Morgan, A.T.; Marsiske, M.; McCrae, C.S. Exercise and Sleep in Community-dwelling Older Adults: Evidence for a Reciprocal Relationship. J. Sleep Res. 2014, 23, 61–68. [Google Scholar] [CrossRef] [PubMed]
  12. Solis-Navarro, L.; Masot, O.; Torres-Castro, R.; Otto-Yáñez, M.; Fernández-Jané, C.; Solà-Madurell, M.; Coda, A.; Cyrus-Barker, E.; Sitjà-Rabert, M.; Pérez, L.M. Effects on Sleep Quality of Physical Exercise Programs in Older Adults: A Systematic Review and Meta-Analysis. Clocks Sleep 2023, 5, 152–166. [Google Scholar] [CrossRef] [PubMed]
  13. Holfeld, B.; Ruthig, J.C. A Longitudinal Examination of Sleep Quality and Physical Activity in Older Adults. J. Appl. Gerontol. 2014, 33, 791–807. [Google Scholar] [CrossRef] [PubMed]
  14. Okifuji, A.; Hare, B. The Association between Chronic Pain and Obesity. J. Pain Res. 2015, 8, 399. [Google Scholar] [CrossRef]
  15. Gulia, K.K.; Kumar, V.M. Sleep Disorders in the Elderly: A Growing Challenge. Psychogeriatrics 2018, 18, 155–165. [Google Scholar] [CrossRef]
  16. Murala, S.; Katyal, N.; Narula, N.; Govindarajan, R.; Sahota, P. Sleep Disorders in Amyotrophic Lateral Sclerosis. RRNMF Neuromuscul. J. 2021, 2, 36–41. [Google Scholar] [CrossRef]
  17. Karabulut, D.; Avci, Ş. Relationship Between Sleep Problems and Gross Motor Function in Children with Cerebral Palsy and Investigation of Their Parents’ Quality of Life. Türk Fiz. Ve Rehabil. Derg. 2020, 31, 180–187. [Google Scholar] [CrossRef]
  18. Campanini, M.Z.; Mesas, A.E.; Carnicero-Carreño, J.A.; Rodríguez-Artalejo, F.; Lopez-Garcia, E. Duration and Quality of Sleep and Risk of Physical Function Impairment and Disability in Older Adults: Results from the ENRICA and ELSA Cohorts. Aging Dis. 2019, 10, 557. [Google Scholar] [CrossRef]
  19. Vincent, B.M.; Johnson, N.; Tomkinson, G.R.; McGrath, R.; Clark, B.C.; Choi, B.-J. Sleeping Time Is Associated with Functional Limitations in a National Sample of Older Americans. Aging Clin. Exp. Res. 2021, 33, 175–182. [Google Scholar] [CrossRef]
  20. Christie, A.D.; Seery, E.; Kent, J.A. Physical Activity, Sleep Quality, and Self-Reported Fatigue across the Adult Lifespan. Exp. Gerontol. 2016, 77, 7–11. [Google Scholar] [CrossRef]
  21. Chodzko-Zajko, W.J.; Proctor, D.N.; Fiatarone Singh, M.A.; Minson, C.T.; Nigg, C.R.; Salem, G.J.; Skinner, J.S. Exercise and Physical Activity for Older Adults. Med. Sci. Sports Exerc. 2009, 41, 1510–1530. [Google Scholar] [CrossRef] [PubMed]
  22. Monteiro, A.M.; Rodrigues, S.; Matos, S.; Teixeira, J.E.; Barbosa, T.M.; Forte, P. The Effects of 32 Weeks of Multicomponent Training with Different Exercises Order in Elderly Women’s Functional Fitness and Body Composition. Medicina 2022, 58, 628. [Google Scholar] [CrossRef] [PubMed]
  23. Carvalho, M.J.; Marques, E.; Mota, J. Training and Detraining Effects on Functional Fitness after a Multicomponent Training in Older Women. Gerontology 2009, 55, 41–48. [Google Scholar] [CrossRef] [PubMed]
  24. Bouaziz, W.; Lang, P.O.; Schmitt, E.; Kaltenbach, G.; Geny, B.; Vogel, T. Health Benefits of Multicomponent Training Programmes in Seniors: A Systematic Review. Int. J. Clin. Pract. 2016, 70, 520–536. [Google Scholar] [CrossRef]
  25. de Asteasu, M.L.S.; Martínez-Velilla, N.; Zambom-Ferraresi, F.; Casas-Herrero, Á.; Izquierdo, M. Role of Physical Exercise on Cognitive Function in Healthy Older Adults: A Systematic Review of Randomized Clinical Trials. Ageing Res. Rev. 2017, 37, 117–134. [Google Scholar] [CrossRef]
  26. Wang, J.; Chen, C.; Zhang, Y. An Investigation of microRNA-103 and microRNA-107 as Potential Blood-Based Biomarkers for Disease Risk and Progression of Alzheimer’s Disease. J. Clin. Lab. Anal. 2020, 34, e23006. [Google Scholar] [CrossRef]
  27. Cadore, E.L.; Izquierdo, M. New Strategies for the Concurrent Strength-, Power-, and Endurance-Training Prescription in Elderly Individuals. J. Am. Med. Dir. Assoc. 2013, 14, 623–624. [Google Scholar] [CrossRef]
  28. Varahra, A.; Rodrigues, I.B.; MacDermid, J.C.; Bryant, D.; Birmingham, T. Exercise to Improve Functional Outcomes in Persons with Osteoporosis: A Systematic Review and Meta-Analysis. Osteoporos. Int. 2018, 29, 265–286. [Google Scholar] [CrossRef]
  29. Bae, S.; Harada, K.; Lee, S.; Harada, K.; Makino, K.; Chiba, I.; Park, H.; Shimada, H. The Effect of a Multicomponent Dual-Task Exercise on Cortical Thickness in Older Adults with Cognitive Decline: A Randomized Controlled Trial. J. Clin. Med. 2020, 9, 1312. [Google Scholar] [CrossRef]
  30. Suzuki, T.; Shimada, H.; Makizako, H.; Doi, T.; Yoshida, D.; Ito, K.; Shimokata, H.; Washimi, Y.; Endo, H.; Kato, T. A Randomized Controlled Trial of Multicomponent Exercise in Older Adults with Mild Cognitive Impairment. PLoS ONE 2013, 8, e61483. [Google Scholar] [CrossRef]
  31. Khan, H.T.; Mari ADDO, K. Factors Affecting Healthy Aging and Its Interconnected Pathways. Turk. J. Healthy Aging Med. 2024, 1, 9–24. [Google Scholar] [CrossRef]
  32. Fanning, J.; Porter, G.; Awick, E.A.; Ehlers, D.K.; Roberts, S.A.; Cooke, G.; Burzynska, A.Z.; Voss, M.W.; Kramer, A.F.; McAuley, E. Replacing Sedentary Time with Sleep, Light, or Moderate-to-Vigorous Physical Activity: Effects on Self-Regulation and Executive Functioning. J. Behav. Med. 2017, 40, 332–342. [Google Scholar] [CrossRef] [PubMed]
  33. Monteiro, A.M.; Bartolomeu, R.F.; Forte, P.; Carvalho, J. The Effects of Three Different Types of Training in Functional Fitness and Body Composition in Older Women. J. Sport Health Res. 2019, 11, 289–304. [Google Scholar]
  34. Cruz-Jentoft, A.J.; Bahat, G.; Bauer, J.; Boirie, Y.; Bruyère, O.; Cederholm, T.; Cooper, C.; Landi, F.; Rolland, Y.; Sayer, A.A.; et al. Sarcopenia: Revised European Consensus on Definition and Diagnosis. Age Ageing 2019, 48, 16–31. [Google Scholar] [CrossRef]
  35. Rikli, R.; Jones, J. Senior Fitness Test Manual, 2nd ed.; Human Kinetics: Champaign, IL, USA, 2013; p. 200. [Google Scholar]
  36. Alcazar, J.; Losa-Reyna, J.; Rodriguez-Lopez, C.; Alfaro-Acha, A.; Rodriguez-Mañas, L.; Ara, I.; García-García, F.J.; Alegre, L.M. The Sit-to-Stand Muscle Power Test: An Easy, Inexpensive and Portable Procedure to Assess Muscle Power in Older People. Exp. Gerontol. 2018, 112, 38–43. [Google Scholar] [CrossRef]
  37. Buysse, D.J.; Reynolds, C.F.; Monk, T.H.; Berman, S.R.; Kupfer, D.J. The Pittsburgh Sleep Quality Index: A New Instrument for Psychiatric Practice and Research. Psychiatry Res. 1989, 28, 193–213. [Google Scholar] [CrossRef]
  38. Del Rio João, K.A.; Becker, N.B.; de Neves Jesus, S.; Isabel Santos Martins, R. Validation of the Portuguese Version of the Pittsburgh Sleep Quality Index (PSQI-PT). Psychiatry Res. 2017, 247, 225–229. [Google Scholar] [CrossRef]
  39. Hopkins, G.; Marshall, S.W.; Batterham, A.M.; Hanin, J. Progressive Statistics for Studies in Sports Medicine and Exercise Science. Med. Sci. Sports Exerc. 2009, 41, 3–12. [Google Scholar] [CrossRef]
  40. Kelter, R. Bayesanova: An R Package for Bayesian Inference in the Analysis of Variance via Markov Chain Monte Carlo in Gaussian Mixture Models. Available online: https://journal.r-project.org/articles/RJ-2022-009/ (accessed on 31 October 2024).
  41. Ly, A.; Verhagen, J.; Wagenmakers, E.-J. Harold Jeffreys’s Default Bayes Factor Hypothesis Tests: Explanation, Extension, and Application in Psychology. J. Math. Psychol. 2016, 72, 19–32. [Google Scholar] [CrossRef]
  42. Koopman, B.O. Harold Jeffreys. Theory of Probability. Oxford University Press, Oxford1939, Vii + 380 Pp. J. Symb. Log. 1943, 8, 34–35. [Google Scholar] [CrossRef]
  43. R: The R Project for Statistical Computing. Available online: https://www.r-project.org/ (accessed on 31 October 2024).
  44. Monteiro, A.M.; Forte, P.; Carvalho, M.J. The Effect of Three Different Training Programs in Elderly Women’s Isokinetic Strength. Motricidade 2020, 16, 84–93. [Google Scholar] [CrossRef]
  45. Taguchi, N.; Higaki, Y.; Inoue, S.; Kimura, H.; Tanaka, K. Effects of a 12-Month Multicomponent Exercise Program on Physical Performance, Daily Physical Activity, and Quality of Life in Very Elderly People with Minor Disabilities: An Intervention Study. J. Epidemiol. 2010, 20, 21–29. [Google Scholar] [CrossRef] [PubMed]
  46. Rodrigues, F.; Jacinto, M.; Figueiredo, N.; Monteiro, A.M.; Forte, P. Effects of a 24-Week Low-Cost Multicomponent Exercise Program on Health-Related Functional Fitness in the Community-Dwelling Aged and Older Adults. Medicina 2023, 59, 371. [Google Scholar] [CrossRef] [PubMed]
  47. Rodrigues, F.; Teixeira, J.E.; Monteiro, A.M.; Forte, P. The Effects of 6-Month Multi-Component Exercise Intervention on Body Composition in Aged Women: A Single-Arm Experimental with Follow-Up Study. Appl. Sci. 2023, 13, 6163. [Google Scholar] [CrossRef]
  48. Forte, P.; Pinto, P.; Barbosa, T.M.; Morais, J.E.; Monteiro, A.M. The Effect of a Six Months Multicomponent Training in Elderly’s Body Composition and Functional Fitness—A before-after Analysis. Motricidade 2021, 17, 34–41. [Google Scholar] [CrossRef]
  49. López-Ortiz, S.; Lista, S.; Valenzuela, P.L.; Pinto-Fraga, J.; Carmona, R.; Caraci, F.; Caruso, G.; Toschi, N.; Emanuele, E.; Gabelle, A.; et al. Effects of Physical Activity and Exercise Interventions on Alzheimer’s Disease: An Umbrella Review of Existing Meta-Analyses. J. Neurol. 2023, 270, 711–725. [Google Scholar] [CrossRef]
  50. Laredo-Aguilera, J.A.; Carmona-Torres, J.M.; García-Pinillos, F.; Latorre-Román, P.Á. Effects of a 10-Week Functional Training Programme on Pain, Mood State, Depression, and Sleep in Healthy Older Adults. Psychogeriatrics 2018, 18, 292–298. [Google Scholar] [CrossRef]
  51. Bademli, K.; Lok, N.; Canbaz, M.; Lok, S. Effects of Physical Activity Program on Cognitive Function and Sleep Quality in Elderly with Mild Cognitive Impairment: A Randomized Controlled Trial. Perspect. Psychiatr. Care 2019, 55, 401–408. [Google Scholar] [CrossRef]
  52. Vu, H.M.; Tran, V.T.H.; Hoang, H.Q.; Han, B.; Hoang, B.X. Efficacy and Tolerability of Ich Nieu Khang Dietary Supplement for Overactive Bladder. J. Med. Food 2023, 26, 262–269. [Google Scholar] [CrossRef]
  53. Torimoto, K.; Uchimura, N.; Roitmann, E.; Marumoto, M.; Hirakata, T.; Burtea, T. A Large Survey of Nocturia Related to Sleep Quality and Daytime Quality of Life in a Young Japanese Population: NOCTURNE Study. Neurourol. Urodyn. 2021, 40, 340–347. [Google Scholar] [CrossRef]
  54. Kanammit, P.; Boonchan, T.; Sirisreetreerux, P.; Viseshsindh, W.; Kochakarn, W. Nocturia and Effect on the Quality of Life. A Study at Ramathibodi Hospital. Insight Urol. 2021, 42, 144–153. [Google Scholar] [CrossRef]
  55. Udo, Y.; Nakao, M.; Honjo, H.; Ukimura, O.; Kitakoji, H.; Miki, T. Sleep Duration Is an Independent Factor in Nocturia: Analysis of Bladder Diaries. BJU Int. 2009, 104, 75–79. [Google Scholar] [CrossRef] [PubMed]
  56. Kohanmoo, A.; Kazemi, A.; Zare, M.; Akhlaghi, M. Gender-Specific Link between Sleep Quality and Body Composition Components: A Cross-Sectional Study on the Elderly. Sci. Rep. 2024, 14, 8113. [Google Scholar] [CrossRef] [PubMed]
  57. Knobbe, T.J.; Kremer, D.; Eisenga, M.F.; van Londen, M.; Annema, C.; Bültmann, U.; Kema, I.P.; Navis, G.J.; Berger, S.P.; Bakker, S.J.L.; et al. Sleep Quality, Fatigue, Societal Participation and Health-Related Quality of Life in Kidney Transplant Recipients: A Cross-Sectional and Longitudinal Cohort Study. Nephrol. Dial. Transplant. 2023, 39, 74–83. [Google Scholar] [CrossRef]
Figure 1. Participants flowchart of sampling.
Figure 1. Participants flowchart of sampling.
Jcm 13 06603 g001
Figure 2. Multicomponent training component volume.
Figure 2. Multicomponent training component volume.
Jcm 13 06603 g002
Figure 3. Correlation heat map. Warm colors signify statistically significant associations, and cold and neutral colors represent statistical insignificance.
Figure 3. Correlation heat map. Warm colors signify statistically significant associations, and cold and neutral colors represent statistical insignificance.
Jcm 13 06603 g003
Table 1. Components and exercises were used day-by-day over the week for the training sessions during the training protocol.
Table 1. Components and exercises were used day-by-day over the week for the training sessions during the training protocol.
ComponentsDay #1 of the WeekDay #2 of the WeekDay #3 of the Week
Warm-up
(5 min)
Jogging and cardio-based warm-up
Dynamic stretching targeting shoulders, hips, and ankles.
Jogging and cardio-based warm-up
Dynamic stretching targeting shoulders, hips, and ankles.
Jogging and cardio-based warm-up
Dynamic stretching targeting shoulders, hips, and ankles.
Resistance training
(1–3 sets; 15–20 min)
1–3 sets, 40–60 s rest between sets
6 repetitions (reps) kettlebell clean and press + 6 reps single-arm kettlebell thrusters
12 reps single-arm kettlebell rows
12 reps kettlebell sumo deadlift high pulls
12 reps dumbbell lateral raises
12 reps single-arm kettlebell triceps extensions
1–3 sets, 40–60 s rest between sets
12 reps alternating single-arm kettlebell rows (touching the ground)
12 reps Romanian deadlifts
12 reps Dumbbell chest flys
12 reps single-arm kettlebell curls
12 reps kettlebell biceps curls
1–3 sets, 40–60 s rest between sets
12 reps single-arm KB swings per side
12 reps KB goblet squats: focus on a slow descent, explosive ascent
12 reps bodyweight lunges: with a 2-s pause at the bottom
12 reps KB Romanian deadlifts
6 reps KB overhead extensions
6 reps triceps kickbacks per side
Balance training
(5–8 min)
(2 sets, IR: 30 s between sets)
Single-leg deadlifts: 3 per leg
Dynamic lateral lunges: 3 per side (hold each lunge position for 3 s)
Alternating high knees: 3 per side (hold each knee up for 3 s)
Reverse lunges with glute squeeze: 6 per leg
Toe touches with step forward: 6 per side (step forward to touch toes)
(2 sets, IR: 30 s between sets)
5 m side shuffle + 2 alternating side lunges + 5 m Jog
10 m heel-to-toe walk
6 high knees with 2 quick taps
(2 sets, IR: 30 s between sets)
Complex [4 high knees with hold + 4 controlled leg swings]
4 toe taps with ankle mobility + 4 static high knees
Single-leg complex [2 controlled leg swings + 2 quick high knees + 2 single-leg balance holds (without touching the ground)]
Aerobic fitness
15–20 min)
3 Sets, 60 s ON, 30 s OFF, IR: 60 s between sets
Marching in place
Light jogging
Light jogging
Step touches
Low-impact jumping jacks
3 Sets, 60 s ON, 30 s OFF, IR: 60 s between sets
Arm circles
Punches (shadow boxing)
Shoulder taps
Front and lateral raises
High knees with arm swing
3 Sets, 60 s ON, 30 s OFF, IR: 60 s between sets
High knees
Arm circles
Step touches
Lateral lunges
Front and lateral raises
Cool down
(5 min)
5 min
Upper and lower body static Stretching: stretches like hamstring stretches, quadriceps stretches, shoulder stretches, and tricep stretches.
Dynamic trunk stretching and breathing exercises: torso twists, side bends, and deep diaphragmatic breathing.
5 min
Upper and lower body static stretching: stretches like hamstring stretches, quadriceps stretches, shoulder stretches, and tricep stretches.
Dynamic trunk stretching and breathing exercises: torso twists, side bends, and deep diaphragmatic breathing.
5 min
Upper and lower body static stretching: stretches like hamstring stretches, quadriceps stretches, shoulder stretches, and tricep stretches.
Dynamic trunk stretching and breathing exercises: torso twists, side bends, and deep diaphragmatic breathing.
Table 2. Mean, standard deviations, percentage of variations, and comparisons for anthropometrics, body composition, physical fitness, and sleep quality measures for the control and experimental groups by moments of evaluations.
Table 2. Mean, standard deviations, percentage of variations, and comparisons for anthropometrics, body composition, physical fitness, and sleep quality measures for the control and experimental groups by moments of evaluations.
Control Group (N = 11)Experimental Group (N = 13)
M1 Mean ± SdM2 Mean ± SdΔ%tpdM1 Mean ± SdM2 Mean ± SdΔ%tpd
Body Mass (Kg)65.64 ± 6.7766.00 ± 5.440%−0.2510.807−0.06863.62 ± 12.9964.75 ± 11.883%−0.7940.443−0.068
Hang Grip (Kgf)26.91 ± 7.8326.72 ± 5.830%0.1100.915−0.00720.08 ± 8.1122.50 ± 5.6412%−1.3510.202−0.007
Arm Curl (Reps)22.27 ± 5.4224.09 ± 3.248%−1.2370.244−0.37318.92 ± 3.0124.31 ± 2.5926%−4.6960.001 *−0.373
Waist circumference (cm)89.73 ± 7.1885.73 ± 8.71−4%1.2980.2230.39185.35 ± 11.8284.79 ± 11.400%0.6380.5350.391
Hip circinferemce (cm)101.82 ± 6.74101.36 ± 3.340%0.2550.8040.08498.46 ± 9.9898.38 ± 10.440%0.1660.8710.084
5TSTS (sg)6.85 ± 1.166.93 ± 1.431%−0.1550.880−0.0587.54 ± 1.116.10 ± 1.24−18%5.392<0.001 *−0.058
CS30 (reps)22.73 ± 2.9423.27 ± 4.472%−0.5340.605−0.16123.85 ± 4.5120.31 ± 3.9919%−8.469<0.001 *−0.161
TUG (sg)5.91 ± 0.7015.41 ± 1.33−7%1.0250.3300.2434.79 ± 0.685.56 ± 1.02−14%4.2120.001 *0.243
Seat and Reach (cm)3.27 ± 5.356.73 ± 9.63106%−0.8790.400−0.265−6.52 ± 11.182.15 ± 6.73−118%−4.1270.001 *−0.265
Back Stretch (cm)−7.46 ± 10.69−4.45 ± 9.32−40%−1.7220.116−0.519−6.89 ± 8.52−3.46 ± 7.63−52%−3.7220.003 *−0.519
2MST (reps)189.18 ± 38.19192.64 ± 62.222%−0.1340.896−0.040174.69 ± 26.85222.08 ± 37.1729%−9.617<0.001 *−0.040
Total Fat (kg)20.55 ± 5.2019.73 ± 4.43−4%0.7260.4840.21320.24 ± 7.1519.59 ± 7.71−3%1.8880.0830.213
Total Fat (%)30.91 ± 5.6929.81 ± 4.77−3%0.8150.4340.22829.42 ± 8.8226.61 ± 9.73−10%2.2250.046 *0.228
Lean Mass (kg)43.09 ± 4.5943.00 ± 3.77−1%0.1150.9110.09441.97 ± 6.1342.40 ± 5.651%−0.7580.4630.094
Body Water (%)48.73 ± 4.0348.55 ± 3.980%0.1760.864−0.00349.38 ± 5.5549.95 ± 5.691%−1.1710.264−0.003
Visceral Fat (a.u.)7.91 ± 2.598.18 ± 2.523%−1.3990.192−0.4227.08 ± 2.636.92 ± 2.33−1%0.5190.613−0.422
MET (Kcal)1341.64 ± 125.611356.91 ± 93.91−19%1.3840.1960.4171304.08 ± 183.171310.54 ± 181.061%−0.5670.5810.417
Sleep Quality (a.u.)4.64 ± 2.346.82 ± 1.1747%−2.8690.017 *−0.8655.46 ± 1.454.62 ± 1.45−14%2.8560.014 *−0.865
Legend: Kg—kilograms; Kgf—Kilograms of force; reps—repetitions; 5TSTS—Five Times Sit-to-Stand Test; CS30—30-Second Chair Stand Test; TUG—Timed Up and Go Test; 2MST—Two-Minute Step Test; MET—Metabolic Rate; * p < 0.05.
Table 3. Results of 32 weeks of multicomponent training in the functional fitness and body composition regarding the interaction with group and time.
Table 3. Results of 32 weeks of multicomponent training in the functional fitness and body composition regarding the interaction with group and time.
VariableMomentExercise (N = 13)Control (N = 11)ANOVABayes FactorSig. Prob.
Body mass (kg)Pre63.6 ± 12.965.6 ± 6.77Time0.31 ± 4.84%Anecdotal
Post64.6 ± 11.866 ± 5.44Group0.38 ± 1.1%Anecdotal
Interaction0.04 ± 1.65%Anecdotal
HG (kgf)Pre20.2 ± 8.1826.9 ± 7.83Time0.37 ± 0.98%Anecdotal
Post22.6 ± 5.6826.7 ± 5.83Group2.41 ± 0.95%Anecdotal
Interaction0.44 ± 2.48%Anecdotal
ULS (rep)Pre18.9 ± 3.0122.3 ± 5.42Time85.02 ± 1.12%Strong
Post24.3 ± 2.5924.1± 3.24Group0.56 ± 0.64%Anecdotal
Interaction80.39 ± 1.76%Strong
Waist (cm)Pre85.5 11.889.9 ± 7.20Time0.44 ± 0.86%Anecdotal
Post84.8 11.485.7 ± 8.72Group0.39 ± 3.49%Anecdotal
Interaction0.08 ± 2.13%Anecdotal
Hip (cm)Pre98.5 ± 9.94102.0 ± 6.74Time0.29 ± 1.32%Anecdotal
Post98.4 ± 10.5101.0 ± 3.36Group0.57 ± 1.7%Anecdotal
Interaction0.06 ± 2.09%Anecdotal
LLP (sec)Pre7.46 ± 1.336.73 ± 1.35Time0.85 ± 0.88%Anecdotal
Post6.08 ± 1.267.09 ± 1.3Group0.37 ± 0.81%Anecdotal
Interaction2.00 ± 3.31%Anecdotal
LLS (rep)Pre20.3 ± 3.9922.7 ± 2.94Time1.92 ± 1.74%Anecdotal
Post23.8 ± 4.5123.3 ± 4.47Group0.43 ± 0.8%Anecdotal
Interaction0.78 ± 2.95%Anecdotal
DB (sec)Pre5.56 ± 1.025.80 ± 0.824Time2.68 ± 0.95%Anecdotal
Post4.78 0.6815.38 ± 1.34Group0.61 ± 2.98%Anecdotal
Interaction0.79 ± 3.6%Anecdotal
LLF (cm)Pre−6.54 ± 11.23.27 ± 5.35Time3.79 ± 0.64%Moderate
Post2.15 ± 6.736.73 ± 9.63Group2.62 ± 0.63%Anecdotal
Interaction7.94 ± 2.16%Strong
ULF (cm)Pre−6.85 ± 8.57−7.46 ± 10.7Time0.82 ± 0.72%Anecdotal
Post−3.46 ± 7.63−4.46 ± 9.32Group0.41 ± 0.56%Anecdotal
Interaction0.80 ± 83.77%Anecdotal
AF (rep)Pre175.0 ± 26.9189.0 ± 38.2Time2.33 ± 0.99%Anecdotal
Post222.0 ± 37.2193.0 ± 62.2Group0.36 ± 0.75%Anecdotal
Interaction1.24 ± 1.78%Anecdotal
Tot. BF (kg)Pre20.3 ± 7.0520.5 ± 5.20Time0.31 ± 2.31%Anecdotal
Post19.7 ± 7.7419.7 ± 4.43Group0.36 ± 0.94%Anecdotal
Interaction0.04 ± 3.85%Anecdotal
BF percentage (%)Pre29.4 ± 8.8030.9 ± 5.63Time0.46 ± 1.09%Anecdotal
Post26.5 ± 9.8129.9 ± 4.66Group0.52 ± 1.41%Anecdotal
Interaction0.10 ± 5.03%Anecdotal
Tot. LM (kg)Pre42 ± 6.0343.3 ± 4.65Time0.30 ± 1.29%Anecdotal
Post42.4 ± 5.7443 ± 3.77Group0.45 ± 7.9%Anecdotal
Interaction0.05 ± 2.41%Anecdotal
Wat. Percentage (%)Pre50 ± 5.1348.7 ± 4.03Time0.29 ± 1.49%Anecdotal
Post50.1 ± 5.7548.7 ± 4.12Group0.50 ± 2.21%Anecdotal
Interaction0.05 ± 2.3%Anecdotal
Visc. Fat (Index)Pre7.08 ± 2.637.91 ± 2.59Time0.30 ± 1.65%Anecdotal
Post6.92 ± 2.338.18 ± 2.52Group0.64 ± 0.98%Anecdotal
Interaction0.07 ± 2.43%Anecdotal
Basal Met.Pre1304 ± 1831669 ± 762Time0.58 ± 1.55%Anecdotal
Post1311 ± 1811357 ± 937Group0.83 ± 0.78%Anecdotal
Interaction0.47 ± 1.64%Anecdotal
Sleep scorePre5.46 ± 1.454.64 ± 2.34Time0.51 ± 3.41%Anecdotal
Post4.62 ± 1.266.82 ± 1.17Group0.56 ± 1.11%Anecdotal
Interaction10.35 ± 2.07%Strong
Table 4. Associations of sleep quality with anthropometrics, body composition, physical fitness variables, and sleep quality for both control and experimental groups, and by moments.
Table 4. Associations of sleep quality with anthropometrics, body composition, physical fitness variables, and sleep quality for both control and experimental groups, and by moments.
GroupVariable AgeBody MassHand GripArm CurlWist CircumferenceHip CircumferenceSTS5TCS30TUGSeat and ReachBach Strech2MSTTotal FatFat PercentageLean MassBody WaterVisceral FattMET
ControlSleep Quality M1r−0.550.1960.30.2820.4270.3920.2370.4260.3780.175−0.2550.441−0.153−0.03−0.1830.3720.036−0.155
p0.0790.5640.370.4020.190.2330.4830.1910.2520.6060.4480.1740.6540.9290.590.260.9170.649
Sleep Quality M2r0.1500.0420.214−0.4180.145−0.1240.082−0.124−0.101−0.014−0.1280.038−0.485−0.0640.1930.665 *0.3860.442
p0.6590.9010.5280.2010.6700.7160.8100.7170.7680.9680.7080.9130.1300.8330.6230.0260.2410.174
ExperimentalSleep Quality M1r−0.0230.364−0.154−0.2010.4540.4850.360−0.2720.575 *0.256−0.0010.0980.562 *0.619 *−0.044−0.646 *0.5150.064
p0.9410.2210.6160.5100.1190.0930.2270.3690.0400.3990.9970.7500.0460.0240.8860.0170.0720.837
Sleep Quality M2r−0.1130.367−0.243−0.0630.2530.3680.492−0.3780.359−0.297−0.1150.3630.5410.620 *−0.052−0.5230.4720.004
p0.7140.2180.4230.8390.4040.2170.0880.2030.2290.3250.7080.2220.0560.0240.8670.0670.1030.991
Legend: 5TSTS—Five Times Sit-to-Stand Test; CS30—30-Second Chair Stand Test; TUG—Timed Up and Go Test; 2MST—Two-Minute Step Test; MET—Metabolic Rate; * p < 0.05.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Forte, P.; Encarnação, S.G.; Branquinho, L.; Barbosa, T.M.; Monteiro, A.M.; Pecos-Martín, D. The Effects of an 8-Month Multicomponent Training Program in Body Composition, Functional Fitness, and Sleep Quality in Aged People: A Randomized Controlled Trial. J. Clin. Med. 2024, 13, 6603. https://doi.org/10.3390/jcm13216603

AMA Style

Forte P, Encarnação SG, Branquinho L, Barbosa TM, Monteiro AM, Pecos-Martín D. The Effects of an 8-Month Multicomponent Training Program in Body Composition, Functional Fitness, and Sleep Quality in Aged People: A Randomized Controlled Trial. Journal of Clinical Medicine. 2024; 13(21):6603. https://doi.org/10.3390/jcm13216603

Chicago/Turabian Style

Forte, Pedro, Samuel G. Encarnação, Luís Branquinho, Tiago M. Barbosa, António M. Monteiro, and Daniel Pecos-Martín. 2024. "The Effects of an 8-Month Multicomponent Training Program in Body Composition, Functional Fitness, and Sleep Quality in Aged People: A Randomized Controlled Trial" Journal of Clinical Medicine 13, no. 21: 6603. https://doi.org/10.3390/jcm13216603

APA Style

Forte, P., Encarnação, S. G., Branquinho, L., Barbosa, T. M., Monteiro, A. M., & Pecos-Martín, D. (2024). The Effects of an 8-Month Multicomponent Training Program in Body Composition, Functional Fitness, and Sleep Quality in Aged People: A Randomized Controlled Trial. Journal of Clinical Medicine, 13(21), 6603. https://doi.org/10.3390/jcm13216603

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop