Main Outcomes of the HEBE Trial: Improving Cardiorespiratory Fitness and Body Composition Through a Tailored Feasible Lifestyle Program
Abstract
1. Introduction
2. Materials and Methods
2.1. Study Design
2.2. Assessments
- Medical history and physical examination, including anthropometric measurements (body weight, height, and waist circumference) and hemodynamics (resting systolic and diastolic blood pressure, heart rate). Biological sampling included fasting plasma glucose and lipid profile. Based on clinical and anthropometric measurements, metabolic syndrome was defined according to guidelines [28].
- Body composition was assessed using bioelectrical impedance analysis [29] (BIA, Bodystat Quadscan 4000, BodyStat Ltd., Sulby, Isle of Man, British Isles, UK), providing estimates of fat mass (FM) and fat-free mass (FFM). The Fat Mass Index (FMi) and Fat-Free Mass Index (FFMi) were calculated to normalize FM and FFM values for height, using the following formulas: FMi = FM (kg)/height (m2); FFMi = FFM (kg)/height (m2).
- Lifestyle
- Cardiopulmonary Fitness Testing
2.3. Lifestyle Prescription Program
2.3.1. Exercise Prescription
2.3.2. Nutrition
2.3.3. Other Lifestyles
2.4. Outcomes
2.5. Statistical Analysis
2.5.1. Analysis of the Main Outcome
2.5.2. Analysis of the Secondary Outcomes
3. Results
3.1. Population
3.2. Main Outcome: Cardiopulmonary Test
3.3. Secondary Outcomes
3.3.1. Functional Parameters
3.3.2. Body Composition Changes
3.3.3. Multivariable Regression Model
3.3.4. Other Lifestyle Components/Parameters
3.3.5. Check of Non-Completers’ Data
4. Discussion
4.1. Cardiorespiratory Fitness to Monitor LMPs
4.2. Body Composition
4.3. LMPs in Clinical Settings
4.4. LMPs and Perceived Well-Being
4.5. Clinical Implications
4.6. Limitations
- -
- It is a single-arm (pre–post) study, a condition which limits the isolation of the effect of the intervention from other experimental variables, unmeasured confounders, and potential observation effects such as the Hawthorne effect. Consequently, the findings should be interpreted with caution, and causal inferences cannot be established. Moreover, we do not have data on long-term follow-up data, and we may not demonstrate the maintenance of behavioural and physiological improvements in the long term.
- -
- The sample size was calculated to detect a clinically relevant increase in VO2max as the primary endpoint, and the follow-up was limited to six months due to funding constraints. In addition to the previous limitations, secondary outcomes were analyzed on a per-protocol basis, which may introduce selection bias and further reduce the effective sample size. Accordingly, inferences for secondary endpoints should be interpreted with caution. The stratified sampling plan ensured adequate representation of key subgroups and improved the precision of estimates within the target population. In addition, a weighted sensitivity analysis was performed to account for potential imbalances across strata, thereby enhancing the robustness of the findings. Nevertheless, the generalizability of the results to a broader population of healthy individuals remains limited, mainly by the study’s eligibility criteria and setting. In particular, the sample consists exclusively of employees of the University of Milan with a very high educational level (59.2% holding a PhD or postgraduate degree), limiting the generalizability of the results to populations with lower health literacy. Moreover, we did not assess the intervention effects after 6 months due to financial restraints.
- -
- This paper focuses primarily on CRF and a subset of clinical variables commonly collected in trials. Other CPX variables were included in the text to provide a clinically meaningful, although not exhaustive, characterization of general cardiopulmonary status, without unnecessarily increasing methodological complexity or overextending the scope of the manuscript. We are planning another manuscript devoted to these data. Moreover, future analyses will explore the multi-omics biomarkers collected during the study to investigate interactions between immunological, metabolic, and autonomic control mechanisms.
- -
- We mainly focused on exercise, which was tailored and prescribed, and it might be most responsible for the observed improvements; however, the counselling given on nutrition and other lifestyle components, albeit limited, might contribute to the observed results. Nevertheless, distinguishing the relative contribution of different lifestyle components may not have significant clinical relevance, considering that the preventive/therapeutic action of lifestyle improvement is more efficacious when all lifestyle components are considered and that improving one lifestyle component (in particular exercise) may also foster improvements in others [82].
- -
- The retrospective registration of the trial may represent a limitation, considering that prospective registration is generally preferred for interventional studies
- -
- We did not report in the present paper the data regarding the assessment of physical activity using a wearable device because we are preparing other papers on these specific (and other) data, considering that the HEBE study was designed to collect many markers and many different papers are planned. Anyway, this specific point was not a main goal of the present study, which focused on cardiorespiratory fitness, the strongest parameter affected by physical training, which may determine health outcomes.
5. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
Abbreviations
| AHA score | American Heart Association score |
| AT | Anaerobic threshold |
| BC | Body composition |
| BMI | Body mass index |
| CI | Confidence interval |
| CNCD | Chronic non-communicable disease |
| CPX | Cardiopulmonary exercise test |
| CRF | Cardiorespiratory Fitness |
| DAP | Diastolic arterial pressure |
| DELTA | Pre–post differences |
| F | Female |
| FM | Fat mass |
| FMi | Fat mass index |
| FFM | Fat-free mass |
| FFMi | Fat-free mass index |
| HDL | High-density lipoprotein |
| HG | Handgrip |
| HR | Heart rate |
| IPAQ | International physical activity questionnaire |
| ITT | Intention-to-treat |
| LDL | Low-density lipoprotein |
| LMPs | Lifestyle modification programs |
| M | Male |
| MAR | Missingness at random |
| METs | Metabolic equivalents |
| METSpeak | Metabolic equivalents at exercise peak |
| MICE | Multiple imputation by chain equations |
| MS | Metabolic syndrome |
| O | Oxygen |
| p0 | Pre-treatment outcome proportions |
| p1 | Post-treatment outcome proportions |
| q25 | 25th percentile |
| q75 | 75th percentile |
| RD | Relative difference |
| SAP | Systolic arterial pressure |
| T0 | Baseline |
| T1 | End of the intervention |
| V | Volume |
| VE | Ventilation |
| VO2max | Volume of maximal oxygen |
| W | Watt |
| 4S-Q | Short–subjective stress-related somatic symptoms questionnaire |
| 6MWT | Six-minute walking test |
| Δ | Delta |
Appendix A
Appendix A.1. Lifestyle Assessment
- -
- Physical activity (total activity volume) was assessed by the International Physical Activity Questionnaire (IPAQ) [36], which focuses on intensity (nominally estimated in Metabolic Equivalents (METs) according to the type of activity) and duration (in minutes) of physical activity, considering the following levels: brisk walking (≈3.3 METs), other activities of moderate intensity (≈4.0 METs) and activities of vigorous intensity (≈8.0 METs). We use the following equations to guess weekly physical activity volume: moderate-intensity [MET·minutes/week] = (3.3 × minutes of brisk walking × days of brisk walking) + (4.0 × minutes of other moderate-intensity activity × days of other moderate-intensity activities); vigorous-intensity: [MET·minutes/week] = 8.0 × minutes of vigorous-intensity activity × days of vigorous-intensity activity; and total weekly physical activity volume [MET·minutes/week] = sum of Moderate + Vigorous MET·minutes/week scores.
- -
- We also assessed the frequency of regular strength and flexibility exercises, considering the following scale: never; sometimes; 1 section/week; 2–3 sections/week; more than 3 sections/week.
- -
- Sedentary behaviour was assessed by asking the number of hours spent in sedentary behaviour (for instance, studying, sitting, driving, TV viewing, computer or smart devices usage) during weekly working days or weekend days.
- -
- Nutrition was assessed using the American Heart Association Healthy Diet Score (AHA score) [37], taking into consideration fruits/vegetables, fish, sweetened beverages, whole grains, and sodium consumption.
- -
- Sleep was assessed by inquiring about the number of hours on average slept every night and asking about the perception of sleep quality
- -
- Stress and somatic symptom perception were assessed using a self-administered questionnaire [30,31,32,33,34,35], providing nominal self-rated scales (higher values indicate higher degrees of symptoms) focusing on: (i) the appraisal of the overall stress and fatigue perception by evaluation scales with integer scores from 0 (‘no perception’) to 10 (‘highest perception’) for each measure; (ii) the Short–Subjective Stress-related Somatic Symptoms Questionnaire (4S-Q), inquiring about four somatic symptoms accounting for the majority of somatic complaints. For scoring purposes, each response will be coded from 0 (‘no feeling’) to 10 (‘a strong feeling’); thus, the total score ranges from 0 to 40. Moreover, we also assessed the following:
- -
- Perception of quality of sleep, quality of health, and quality of life were assessed using evaluation scales from 0 (‘worst quality) to 10 (‘best quality’) for each measure.
- -
- Smoke behaviour: We considered non-smokers all subjects who reported having never smoked or having stopped smoking for more than one year.
- -
- We enquired about the usage of alcohol, considering Italian habits, asking about the number of glasses of wine or beer consumed per week and the number of glasses of spirits consumed per week.
- -
- Gum bleeding was evaluated considering the following choices: “yes”, “no”, or “sometimes”.
- -
- Work-related discomfort was evaluated considering the following choices: “no”, “sometimes”, “yes”, or “no response”.
Appendix A.2. Ongoing Multi-Omics Analysis and Study of the Autonomic Nervous System (ANS)
| Variable | |
|---|---|
| Age (years): median (q25–q75) | 51.1 (45.0–56.2) |
| Role: | |
| UNIMI Faculty | 38 (38.8%) |
| Technical and Administrative Staff | 45 (45.9%) |
| Researcher | 15 (15.3%) |
| Gender: Female | 52 (53.1%) |
| Education Level | |
| High School Diploma | 4 (4.1%) |
| Bachelor’s Degree | 26 (26.5%) |
| PhD/Postgraduate Specialization | 68 (59.2%) |
| Frequency of medical consultations for | |
| health status assessment | |
| Never | 1 (1.0%) |
| Once per year | 42 (42.9%) |
| Once every 2 years | 3 (3.1%) |
| Regularly for specific medical issues | 14 (14.3%) |
| Only when experiencing illness | 38 (38.8%) |
| Presence of Chronic Disease | |
| No | 71 (72.4%) |
| Yes | 23 (23.5%) |
| No response | 4 (4.1%) |
| Work-related Discomfort | |
| No | 57 (58.2%) |
| Sometimes | 27 (27.6%) |
| Yes | 13 (13.3%) |
| No response | 1 (1.0%) |
| Lifestyle Goals for Improvement | |
| Eating a healthier diet | 22 (22.4%) |
| Becoming more physically active | 52 (53.1%) |
| Managing stress | 21 (21.4%) |
| Quitting smoking | 3 (3.1%) |
| T0 Median, 25th–75th Percentile Unweighted | T1 Median, 25th–75th Percentile Unweighted | Median Difference Between T1 and T0 | |
|---|---|---|---|
| Fasting Blood Glucose (mg/dL) | 89 (85; 96) | 90 (83; 95) missing: 4 (4.3%) | −2.0 (−7.3, 3.3) missing: 4 (4.3%) |
| Triglycerides (mg/dL) | 82 (62; 118) | 74 (61; 92) missing: 4 (4.3%) | −6.0 (−14.6, 2.6) missing: 4 (4.3%) |
| Total Cholesterol (mg/dL) | 210 (179; 232) | 188 (170; 218) missing: 4 (4.3%) | −8.0 (−16.2, 0.2) missing: 4 (4.3%) |
| HDL Cholesterol (mg/dL) | 60 (50;70) | 55 (50; 71) missing: 4 (4.3%) | −1.0 (−4.4, 2.4) missing: 4 (4.3%) |
| LDL Cholesterol (mg/dL) | 124 (104; 147) | 112 (96; 133) missing: 4 (4.3%) | −7.0 (−15.0, 1.0) missing: 4 (4.3%) |
| Satisfaction with the Program: median (q25; q75) | 8 (8; 10) |
| No response | |
| Perceived Difficulty in Following Program: median (q25; q75) | 7 (3.7 (7.6%)3; 8) |
| No response | 7 (7.6%) |
| Overall Perception of Well-Being | |
| Much Worse | 0 (0.0%) |
| Worse | 1 (1.1%) |
| No Change | 6 (6.5%) |
| Improved | 56 (60.9%) |
| Much Improved | 21 (22.8%) |
| No response | 8 (8.7%) |
| Reasons for Non-Adherence * (N = 63) | |
| Lack of Time | 42 (66.7%) |
| Motivation Issues | 7 (11.1%) |
| Difficulty Following the Program | 4 (6.3%) |
| Health Issues | 16 (25.4%) |
| Other Reasons | 8 (12.7%) |
| T0 N (%) | T1 N (%) | Probability of: | Relative Difference Between T1 and T0 | |
|---|---|---|---|---|
| Smoke Non-smoker/ex-smoker Smokers Missing | 87 (94.6%) 5 (5.4%) - | 84 (91.3%) 4 (4.3%) 4 (4.3%) | Being non-ssmoker OR former smoker: | 0.7% (−1.7, 3.2%) |
| Gum Bleeding No Sometime Yes Missing | 79 (85.9%) 0 (0.0%) 13 (14.1%) - | 79 (85.9%) 5 (5.4%) 4 (4.3%) 4 (4.3%) | No bleeding: | 4.6% (−12.2%, 24.6%) |
| Flexibility exercise (Stretching) No sometimes 1 session/week 2–3 sessions/week More than 3 sessions/week Missing | 49 (53.3%) 24 (26.1%) 8 (8.7%) 8 (8.7%) 3 (3.3%) - | 26 (28.3%) 20 (21.7%) 25 (27.2%) 11 (12.0%) 6 (6.5%) 4 (4.3%) | Doing weekly stretching (any frequency) | 37.2% (−3.4%, 95.0%) |
| Strength Exercises No sometimes 1 session/week 2–3 sessions/week More than 3 sessions/week Missing | 21 (22.8%) 49 (53.3%) 21 (22.8%) 1 (1.1%) 0 (0.0%) - | 21 (22.8%) 41 (44.6%) 26 (28.3%) 0 (0.0%) 0 (0.0%) 4 (4.3%) | Doing weekly exercise (any frequency) | 3.0% (−14.7%, 24.4%) |
| Parameter | T0 Median, 25th–75th Percentile Unweighted | T1 Median, 25th–75th Percentile Unweighted | Median Difference Between T1 and T0 |
|---|---|---|---|
| METs TOT (MET·minutes/week) | 1114 (511; 1760) | 1774 (1094; 2449) | 434 (44, 824) |
| - | 4 (4.4%) | 4 (4.4%) | |
| Sedentary behaviours (hours) * | 55 (48; 65) | 51 (41; 59) | −5 (−8.5, −1.5) |
| missing | 2 (2.2%) | 7 (7.8%) | 9 (9.8%) |
| Wine/beer (glasses/week) | 2 (0; 4) | 1 (0; 3) | 0 (−1.0, 0.0) |
| missing | 1 (1.1%) | 9 (10.0%) | 10 (10.9%) |
| Spirits (glasses/week) | 0 (0; 0) | 0 (0; 0) | 0 ** |
| missing | 1 (1.1%) | 7 (7.8%) | 8 (8.7%) |
| 4SQ score (a.u.) | 6 (2; 15) | 4 (0; 12) | −1.0 (−3.7, 1.7) |
| missing | - | 4 (5.5%) | 5 (5.5%) |
| Stress Perception score (a.u.) | 5.0 (2.8; 8.0) | 4.0 (2.0; 7.0) | −1.0 (−2.6, 0.6) |
| missing | - | 4 (4.4%) | 4 (4.4%) |
| Fatigue Perception score (a.u.) | 7.0 (3.0; 8.0) | 4.0 (3.0; 8.8) | −1.0 (−2.6, 0.6) |
| missing | - | 4 (4.4%) | 4 (4.4%) |
| AHA healthy diet score (a.u.) | 2.5 (2.0; 3.0) | 3.0 (2.0; 4.0) | 0.0 (−0.3, 0.3) |
| missing | - | 4 (4.4%) | 4 (4.4%) |
| Sleep (hours/day) | 7.0 (6.0; 7.0) | 7.0 (6.0; 7.0) | 0 ** |
| missing | - | 4 (4.4%) | 4 (4.4%) |
| Perception of sleep quality (a.u.) | 6.0 (5.0; 8.0) | 7.0 (6.0; 8.0) | 0 (−0.6, 0.6) |
| missing | - | 4 (4.4%) | 4 (4.4%) |
| Perception of health quality (a.u.) | 7.0 (6.0; 8.0) | 8.0 (7.0; 8.0) | 1 (−0.6, 2.6) |
| missing | - | 4 (4.4%) | 4 (4.4%) |
| Perception of job performance (a.u.) | 7.0 (6.0; 8.0) | 8.0 (7.0; 8.0) | 0 (−1.2, 1.2) |
| missing | - | 4 (4.4%) | 4 (4.4%) |
| Parameter | Completers (n = 92) | Non-Completers (n = 6) | Cramer V |
|---|---|---|---|
| Gender | 0.404 | ||
| Female | 51 (55.4%) | 1 (16.7%) | |
| Male | 41 (44.6%) | 5 (83.3%) | |
| Physical activity | 0.082 | ||
| <600 MET minutes/week | 54 (58.7%) | 4 (66.7%) | |
| ≥600 MET minutes/week | 38 (41.3%) | 2 (33.3%) | |
| AHA score | 0.188 | ||
| 0–1 | 16 (17.4%) | 2 (33.3%) | |
| 2–3 | 60 (65.2%) | 3 (50.0%) | |
| 4–5 | 16 (17.4%) | 1 (16.7%) | |
| Metabolic syndrome | 0.093 | ||
| No | 69 (75.8%) | 5 (83.3%) | |
| Yes | 22 (24.2%) | 1 (16.7%) |

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| 1° VISIT ACTIONS | AIMS |
|---|---|
| Welcome |
|
| Clinical history and clinical assessment |
|
| Explanation of diagnosis and specific benefits derived from lifestyle change |
|
| Setting specific individual goals |
|
| Education about physical activity/nutrition, tailored exercise prescription, and optimization of nutritional habits |
|
| VO2max (mL/kg/min) | Baseline (T0) Mean, sd | End Treatment (T1) Mean, sd | Pre–Post Difference: Est (95% CI) | Pre–Post Difference: t, df, p |
|---|---|---|---|---|
| Intention-to treat Sensitivity analysis | 27.3, 6.9 26.9, 6.7 | 30.1, 8.0 29.4, 7.6 | 2.86 (2.23, 3.55) 2.45 (1.76, 3.14) | 9.03, 78.3, <0.0001 * 6.95, 60.3, <0.0001 * |
| Per-protocol Sensitivity analysis | 27.4, 7.1 27.0, 6.9 | 30.2, 8.0 29.5, 7.7 | 2.95 (2.32, 3.57) 2.45 (1.85, 3.05) | 9.35, 84, <0.0001 * 8.15, 76, <0.0001 * |
| Parameter | T0 Median, (q25; q75) | T1 Median, (q25; q75) | Difference Between T1 and T0 (est, 95% CI) | Difference Between T1 and T0 (Sensitivity Analysis) |
|---|---|---|---|---|
| Load (Watt) * | 168 (127; 197) | 176 (136; 224) | 14.0 (7.3, 20.7) | 12.0 (5.0, 21.0) |
| FC rest (b/min) | 79 (72; 88) | 79 (72; 87) | 0.0 (−4.5, 4.5) | 0.0 (−3.0, 6.0) |
| FC peak (b/min) | 165 (156; 173) | 167 (157; 176) | 2.0 (−0.6, 4.6) | 0.0 (−2.0, 4.0) |
| SAP rest (mmHg) * | 120 (110;120) | 110 (110; 116) | −10.0 (−18.3, −1.7) | −10.0 (−10.0, 0.0) |
| SAP peak (mmHg) | 160 (150; 180) | 160 (150; 170) | 0.0 (−3.4, 3.4) | 0.0 (0.0, 10.0) |
| DAP rest (mmHg) | 80 (70;80) | 70 (70; 80) | −5.0 (−14.7, 4.7) | −10.0 (−10.0, 0.0) |
| DAP peak (mmHg) | 80 (80;80) | 80 (70; 80) | 0 (−2.5, 2.5) | 0.0 (0.0, 15.0) |
| VE/VCO2 slope | 26 (24; 29) | 26 (24; 29) | −0.03 (−1.4, 1.1) | −0.03 (−1.91, 1.70) |
| VO2/Work(mL/min)/Watt) | 9.7 (9;10) | 9.8 (9.1; 10) | 0.04 (−0.39, 0.43) | −0.14 (−0.73, 0.50) |
| AT % peak VO2 * | 76 (68; 85) | 86 (84; 88) | 9.0 (4.3, 13.7) | 6.0 (2.0, 16.0) |
| AT Load (Watt) * | 123 (98; 147) | 147 (112; 196) | 28.0 (12.7, 43.3) | 21.0 (8.0, 35.0) |
| AT VO2 (mL/min/kg) * | 22 (18;25) | 26 (22; 31) | 4.5 (2.6, 6.4) | 3.3 (1.7, 5.9) |
| METs peak * | 8.5 (7.1; 10.0) | 9.4 (8; 11) | 0.7 (0.3, 1.1) | 0.6 (0.3, 1.3) |
| 6MWT (m) * | 648 (604; 682) | 678 (630; 720) | 27.0 (13.5, 40.5) | 30.0 (9.0, 57.0) |
| HG right arm mean (Kg) | 36 (28; 43) | 35 (27; 43) | 0.2 (−0.8, 1.2) | 0.5 (−0.9, 1.4) |
| HG left arm mean (Kg) | 32 (26; 40) | 31 (27; 40) | 0.6 (−0.2, 1.5) | 0.7 (−0.4, 1.9) |
| Parameter | T0 Median, (q25; q75) | T1 Median, (q25; q75) | Difference Between T1 and T0 (est, 95% CI) | Difference Between T1 and T0 (Sensitivity Analysis) |
|---|---|---|---|---|
| Height (cm) | 172 (166; 177) | - | - | - |
| Weight (Kg) | 74 (67; 90) | 74 (64; 83) | −1.5 (−3.3, 0.3) | −1.0 (−2.0, 1.0) |
| Hydration (%) | 74 (73; 74) | 74 (73; 74) | 0.1 (−0.06, 0.3) | 0.2 (0.1, 0.6) |
| Waist Circumference (cm) * | 92 (83; 100) | 88 (79; 95) | −3.0 (−5.8, −0.2) | −2.0 (−4.0, 0.0) |
| BMI (kg/m2) * | 26 (23; 28) | 24 (23; 27) | −0.5 (−1.0, −0.1) | −0.4 (−0.8, 0.2) |
| Fat-Free Mass (Kg) | 58 (48; 64) | 59 (48; 65) | 0.8 (−0.2, 1.8) | 0.7 (−0.1, 2.2) |
| Fat Mass (Kg) * | 19 (13; 24) | 15 (11; 20) | −3.3 (−5.1, −1.5) | −2.7 (−4.7, −0.6) |
| Total Body Water (L) | 43 (34; 48) | 45 (35; 48) | 0.7 (−0.01, 1.4) | 0.7 (0.0, 1.3) |
| Body Cellular Mass (%) | 30 (24; 35) | 30 (25; 35) | 0.2 (−0.5, 0.9) | 0.3 (−0.6, 1.3) |
| Fat-Free Mass (%) * | 75 (68; 80) | 79 (74; 84) | 3.7 (1.6, 5.8) | 3.7 (1.2, 5.9) |
| Fat Mass (%) * | 25 (20; 32) | 21 (16; 27). | −3.7 (−5.8, −1.6) | −3.7 (−5.4, −0.4) |
| Total Body Water (%) * | 55 (50; 59) | 58 (55; 62) | 2.9 (1.4, 4.4) | 2.9 (0.6, 4.3) |
| Fat Mass Index (FMi) * | 0.00069 (0.00046; 0.00085) | 0.00051 (0.00038; 0.00068) | −0.00011 (−0.00018, −0.00005) | −0.000099 (−0.00017, −0.00002) |
| Fat-Free Mass Index (FFMi) | 19 (18; 22) | 19 (18; 21) | 0.3 (−0.1, 0.6) | 0.3 (−0.1, 0.6) |
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Lucini, D.; Rota, F.; Marano, G.; Oggionni, G.; Luconi, E.; Iodice, S.; Bianchi, F.; Mandò, C.; Bernardelli, G.; Malacarne, M.; et al. Main Outcomes of the HEBE Trial: Improving Cardiorespiratory Fitness and Body Composition Through a Tailored Feasible Lifestyle Program. Nutrients 2026, 18, 1918. https://doi.org/10.3390/nu18121918
Lucini D, Rota F, Marano G, Oggionni G, Luconi E, Iodice S, Bianchi F, Mandò C, Bernardelli G, Malacarne M, et al. Main Outcomes of the HEBE Trial: Improving Cardiorespiratory Fitness and Body Composition Through a Tailored Feasible Lifestyle Program. Nutrients. 2026; 18(12):1918. https://doi.org/10.3390/nu18121918
Chicago/Turabian StyleLucini, Daniela, Federica Rota, Giuseppe Marano, Gianluigi Oggionni, Ester Luconi, Simona Iodice, Francesca Bianchi, Chiara Mandò, Giuseppina Bernardelli, Mara Malacarne, and et al. 2026. "Main Outcomes of the HEBE Trial: Improving Cardiorespiratory Fitness and Body Composition Through a Tailored Feasible Lifestyle Program" Nutrients 18, no. 12: 1918. https://doi.org/10.3390/nu18121918
APA StyleLucini, D., Rota, F., Marano, G., Oggionni, G., Luconi, E., Iodice, S., Bianchi, F., Mandò, C., Bernardelli, G., Malacarne, M., Castaldi, S., Boracchi, P., Bollati, V., Clerici, M., Biganzoli, E. M., & on behalf of the HEBE Consortium. (2026). Main Outcomes of the HEBE Trial: Improving Cardiorespiratory Fitness and Body Composition Through a Tailored Feasible Lifestyle Program. Nutrients, 18(12), 1918. https://doi.org/10.3390/nu18121918

