Trigger Point Therapy Techniques as an Effective Unconventional Method of Treating Tension Headaches: A Systematic Review
Abstract
:1. Introduction
- Are various trigger points therapy techniques effective in treatment of tension-type headaches?
- How trigger points therapy affect physical and psychological variables in tension-type headaches?
2. Materials and Methods
2.1. Eligibility Criteria
2.2. Search Strategy
2.3. Data Extraction and Evaluation of the Methodological Quality of Studies
3. Results
4. Discussion
5. Conclusions
- Trigger point therapy has reduced the duration, intensity, and frequency of headaches.
- Dry needling, ischaemic compression, positional relaxation techniques, and massage protocols focused on deactivating trigger points are effective methods of unconventional treatment of tension-type headaches.
Author Contributions
Funding
Conflicts of Interest
References
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Studies | Participants | Interventions | Comparisons | Outcomes |
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Reference | Type of Study | Participants, Diagnosis of TTH | Treatment | Control Group/Comparators | Type of TrP | Treated Muscles |
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Abaschian et al., 2020 [23] | RCT | n = 21 (investigation group—12 women, CG—9 women). ETTH was based on ICHD-3. criteria. | dry needling with passive stretching | passive stretch session only | active or latent | upper trapezius, sternocleidomastoid, temporalis |
Berggreen et al., 2011 [24] | RCT | n = 35 (19—massage treatment; 16—CG); CTTH diagnosis was based on 1988 International Headache Society (IHS) criteria | ischaemic compression | no treatment | active | m. sternocleidomastoid, masseter muscle, m. temporalis, medial and lateral pterygoid muscles, anterior neck muscles, facial muscles, occipitofrontalis muscles, splenius capitis and splenius cervicis muscles, posterior cervical muscles, suboccipital muscles |
Gildir et al., 2019 [25] | RCT | n = 160 (study group n = 80, control group n = 80); diagnosis of CTTH was based on the International Classification of Headache Disorders, 3rd edition beta version) (ICHD-3 beta criteria) | dry needling of active TrPs | placebo group—sham dry needling (into adipose tissue without TrPs) | active | upper trapezius, masseter, temporalis, frontalis, splenius cervicis and capitis, suboccipital |
Kamali et al., 2019 [26] | RCT | n = 40 (20—friction massage group; 20—dry needling group); no information about TTH diagnosis criteria | 2 groups—dry needling and friction massage | lack of CG—two different physiotherapy methods | active or latent | suboccipital, temporalis, SCM, and upper trapezius muscles |
Mohamadi, Ghanbari, Rahimi Jaberi 2012 [27] | case report | n = 1; no information about TTH diagnosis criteria | Positional Release Therapy | lack of CG | active | right trapezius, left sternocleidomastoid, right and left obliqus capitis superior, left rectus capitis anterior |
Mohamadi et al., 2020 [28] | RCT | n = 32 (SG—16, CG—16); diagnosis of TTH was based on the International Headache Society criteria (2004) | Positional Release Technique | lack of intervention | active | trapezius, sternocleidomastoid, obliquscapitis superior, rectus capitis anterior, rectus capitis posterior, interspinalis, and multifidus |
Moraska, Chandler, 2008 [29] | pilot study | n = 16; (13—CTTH; 3—ETTH); the diagnosis of TTH was based on the International Headache Society criteria (2004) | massage focused on TrP | lack of CG | active | upper trapezius, sternocleidomastoid, suboccipital, and splenius capitis. |
Moraska et al., 2015 [30] | RCT | n = 56 (17—massage group, 19—placebo group, 20—wait-list); TTH diagnosis was based on International Classification of Headache Disorders, 2nd edition (ICHD-2) | massage focused on TrP | placebo group- detuned ultrasound; wait-list group | active | upper trapezius, suboccipital muscles, sternocleidomastoid |
von Stülpnagel et al., 2009 [31] | pilot study | n = 9; children; TTH diagnosis was based on the criteria of the International Headache Society | trigger point–specific physiotherapy—ischaemic compression, local stretching of the taut band, active and passive stretching of the muscle combined with postisometric relaxation. | lack of CG | active | sternocleidomastoid, splenius capitis, upper trapezius, temporalis, semispinalis, levator scapulae, masseter, and frontalis muscles |
Outcomes | Side Effects | |||||||
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Reference | Methods | General Outcomes | Pain Frequency | Pain Intensity | Pain Duration | Other | Follow-Up | |
Abaschian et al., 2020 [23] | headache diary -intensity and frequency of headache; quality of life—SF-36; depression symptoms—Beck questionnaire | The intensity of tension-type headaches in the intervention group decreases statistically significantly after one month of intervention (p = 0.017). In the control group, the intensity of the headache increased after one month of intervention (p = 0.023). “One month after the intervention, there was a significant difference between the changes in headache intensity in the two groups (p = 0.003)”. Statistically, changes in headache frequency were significant after 4 weeks of intervention in the intervention group (p = 0.021), but they were not significant in the control group (p = 0.805). “There was a significant difference between the frequency changes of headache between two groups after 4 weeks of intervention (p = 0.018)”. | IG—baseline 11.08 (3.60), after 1 month—10.33 (3.67); p = 0.021 * CG—baseline 11.44 (3.77), after 1 month 11.77 (3.96) p = 0.805 [days per month] | IG—baseline 6.08 (1.23), after 1 month 5.52 (1.07); p = 0.017 * CG—baseline 4.83 (1.14), after 1 month 5.12 (1.08) p = 0.023 * [VAS 0–10] | ND | physical functioning— there was a significant difference between the control and intervention groups (p = 0.008) in terms of changes in physical functioning and quality of life. In the other areas of quality of life (role limitations, vitality, mental health, social health, bodily pain, genetal health), there was no significant difference between the two groups of intervention and control. | 1 month after treatment | ND |
p-value between group = 0.018 * | p-value between group = 0.003 * | |||||||
Berggreen et al., 2011 [24] | headache diary—intensity (morning and evening pain, pain inconvenience and medicine consumption); McGill’s Pain Questionnaire (MPQ); number of TrPs—palpation; quality of life—SF-36 | “The intention-to-treat analysis of the primary outcome (pain intensity in the morning), showed a significant decrease compared with the control group (difference 8.8 mm [95% CI 0.11—17.4], p = 0.047)”. “There were no significant differences between the treatment group and the control group for evening” (difference 3.4 mm [95% CI 9.3—16.0], p = 0.594). | ND | morning pain: TG—before treatment 28.0 (15.9), after treatment 16.2 (11.8), CG—before treatment 26.6 (12.6), after treatment 24.9 (14.5) | ND | VAS inconvenience morning and evening— no significant differences between the treatment group and the control group numer of TrPs— TG before treatment 37.9, after treatment 12.6; CG before treatment 43.2, after treatment 42.1, difference in the change: 31.2 [95% CI 20.8–41.5]) medicine consumption—TG before treatment 111.7 mg/day, after treatment 64.1 mg/day, CG before treatment 75.9 mg/day, after treatment 84.6 mg/day MPQ and SF-36—“There were no signifi cant differences between the treatment group and the controlgroup for MPQ pain score or SF-36 score” | - | ND |
p-value between group = 0.047 * | ||||||||
evening pain: TG—before treatment—34.7 (21.9), after treatment—22.2 (21.4), CG -before treatment 29.8 (18.2), after treatment 25.5 (16.3) | ||||||||
p-value between groups = 0.594 | ||||||||
Gildir et al., 2019 [25] | headache diary—TTH intensity, frequency and duration; quality of life—Turkish version of SF-36 | “trigger point dry needling in patients with CTTH is effective and safe in reducing headache frequency, intensity and duration, and increasing health-related quality of life. Effectiveness of treatment begins in the first week of treatment and continues throughout the second week and follow-up periods” (1 month). | SG: before treatment 18.5 ± 2.7 after treatment 3.8 ± 1.8; CG: before treatment 18 ± 2.4 after treatment 7.9 ± 2.0 [day per month] p-value between group <0.05 | SG: before treatment 4.5 ± 1.0 after treatment 0.7 ± 0.8; CG: before treatment 4.6 ± 1.2, after treatment 4.6 ± 0.7 [VAS 0–10 cm] p-value between group <0.05 | SG: before treatment 3.9 ± 0.7, after treatment 0.7 ± 0.8; CG: before treatment 3.8 ± 0.9, after treatment 3.9 ± 1.0 [hours per day] p = 0.001 | quality of life—Compared to the control group, the study group showed significantly lower results in all quality of life aspects (physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, mental health) after the treatment (p = 0.001). | after 4 weeks; pain intensity: SG 0.9 ± 0.9, CG 4.9 ± 0.7 [VAS 0–10 cm] pain frequency: SG 4.9 ± 2.8, CG 16.3 ± 2.6 [day per month]; pain duration: SG 0.7 ± 0.6, CG: 4.1 ± 0.8 [hours per day] | “Five of the patients in each group experienced pain and fear during the procedure”. |
Kamali et al., 2019 [26] | headache frequency, headache intensity; pressure pain threshold–algometry; cervical range of motion—goniometer | “The results showed that both treatment methods significantly reduced headache frequency and intensity, and increased pain threshold at the trigger points” (p < 0.05). “Between-group comparisons showed that dry needling increased pain threshold significantly more than friction massage”. | DN group—baseline 5.00, after treatment1.95 ± 2.08, p < 0.05; FM group—7.00, after treatment 2.85 ± 2.56, p < 0.05 [days a week] | DN group—baseline 8.00, after treatment 3.00 ± 2.31, p < 0.05; FM group— baseline 9.50, after treatment4.22 ± 3.51, p < 0.05 [VAS 0–10] | ND | pressure pain treshold—DN group before treatment 1.07 (median), after treatment 1.27 ± 0.25 (mean ± SD), FM group before treatment 0.86 (median), after treatment 1.12 ± 0.42 (mean ± SD), between-group comparison after treatment—0.008 cervical range of motion | - | ND |
p-value between group = 0.7 | p-value between group = 0.4 | |||||||
Mohamadi, Ghanbari, Rahimi Jaberi 2012 [27] | Pain intensity—Numeric Pain Index (NPI) | “After 3 treatment sessions, the patient’s headache stopped completely. Throughout the next 8 months, she had no pain and did not use any medication. Unfortunately, after this time and following a family conflict, her headache returned”. | ND | before treatment—10; after first session—10; after second session—8; after third session—0 [NPI 0–10] | ND | ND | “Throughout the next 8 months, she had no pain and did not use any medication”. | ND |
Mohamadi et al., 2020 [28] | headache diary—headache frequency and intensity; PPT—algometry; protone resonance spectroscopy; McGill Pain Questionnaire | Headache frequency (p = 0.001) and intensity (p = 0.002) decreased significantly in the PRT group after treatment. | SG: before treatment 18.30 ± 6.29, after treatment 5.84 ± 3.76, p = 0.001 * CG: before treatment 16.69 ± 6.14, after treatment 17.30 ± 6.57, p = 0.36 [days per month] | SG: before treatment 7.46 ± 1.80, after treatment 4.38 ± 1.66, p = 0.002 * CG: before treatment 6.53 ± 1.89, after treatment 7.00 ± 1.47, p = 0.14 [0–10] | ND | metabolite profile—SG: no significant changes after treatment, CG: no significant changes in any variables except M-Ino/Cr ratio in the somatosensory cortex, which increased significantly (p = 0.041). McGill score—McGill score (p = 0.003) decreased significantly in the PRT group aftertreatment. Statistically significant differences between groups were found (F1,22 = 24.02; p < 0.001; eta = 0.52) local PPT: SG before treatment 1.99 ± 0.55, after treatment 2.60 ± 0.74 (p = 0.003), CG before treatment 2.34 ± 0.84, after treatment 2.33 ± 0.81 (p = 0.88). distal PPT: SG before treatment 6.10 ± 1.63, after treatment 6.53 ± 1.36 (p = 0.23), CG before treatment 5.01 ± 1.49, after treatment 4.79 ± 1.66 (p = 0.19). Statistically significant differences between groups were found for local PPT (F1,22 = 10.31, p = 0.004, eta = 0.32) and distal PPT (F1,22 = 4.72, p = 0.04, eta = 0.17). | - | ND |
p-value between group < 0.001 * | p-value between group < 0.001 * | |||||||
Moraska, Chandler, 2008 [29] | headache diary—frequency (primary outcome) and peak intensity, duration (secondary outcome) | “Headache frequency decreased from 4.7 ± 0.7 episodes per week during baseline to 3.7 ± 0.9 during treatment period 2 (p < 0.05); reduction was also noted during the follow-up phase (3.2 ± 1.0). Secondary measures of headache also decreased across the study phases with headache intensity decreasing by 30% (p < 0.01) and headache duration from 4.0 ± 1.3 to 2.8 ± 0.5 h (p < 0.05)”. | CTTH group—baseline: 5.33 ± 0.54, 3 weeks 4.93 ± 0.75; 6 weeks 4.28 ± 0.88; follow up 3.67 ± 1.18 ETTH group- baseline 2.57 ± 0.85; 3 weeks 2.57 ± 1.71; 6 weeks 1.00 ± 0.33; follow-up 1.33 ± 0.33 [days per week] p < 0.01 | CTTH group—baseline 43.2 ± 6.30; 3 weeks 38.7 ± 9.18; 6 weeks 31.9 ± 9.39; follow-up 32.8 ± 10.3 ETTH group—baseline 60.3 ± 22.5; 3 weeks 41.2 ± 20.0; 6 weeks 43.1 ± 28.4; follow-up 40.6 ± 23.2 [VAS 0–100 mm] p = 0.001 | CTTH group—baseline 3.58 ± 1.10; 3 weeks 3.96 ± 1.01; 6 weeks 2.85 ± 0.70; follow-up 2.70 ± 0.48 ETTH group—baseline 5.73 ± 5.38; 3 weeks 4.77 ± 3.80; 6 weeks 5.37 ± 3.93; follow-up 2.90 ± 1.65 [hours] p < 0.05 | Headache Disability Index questionnaire: HDI- Total: CTTH group—baseline: 43.6 ± 7.66, 3 weeks 34.0 ± 9.55; 6 weeks 23.3 ± 10.6; follow up 26.4 ± 9.20 ETTH group—baseline 47.0 ± 29.1; 3 weeks 40.6 ± 34.6; 6 weeks 33.4 ± 14.6; follow-up 26.6 ± 10.2 HDI- Emotional: CTTH group—baseline: 17.8 ± 3.58, 3 weeks 14.3 ± 4.19; 6 weeks 9.08 ± 4.32; follow up 9.85 ± 4.18 ETTH group—baseline 19.0 ± 13.1; 3 weeks 15.3 ± 12.9; 6 weeks 10.7 ± 7.28; follow-up 7.33 ± 3.46 HDI—Functional: CTTH group—baseline: 25.8 ± 4.80, 3 weeks 19.7 ± 5.66; 6 weeks 14.2 ± 6.57; follow up 16.5 ± 5.34 ETTH group—baseline 28.0 ± 16.1; 3 weeks 25.3 ± 21.8; 6 weeks 22.7 ± 7.96; follow-up 19.3 ± 6.92 | after 3 weeks | ND |
Moraska et al., 2015 [30] | headache diary—frequency, intensity, and duration, medication use (dose/wk); PPT—algometry; quality of life—Headache Disability Inventory, Headache Impact Test (HIT-6); perceived clinical change | “…group differences across time were detected in HA frequency (p = 0.026), but not for intensity or duration. Post hoc analysis indicated that HA frequency decreased from baseline for both massage (p < 0.0003) and placebo (p = 0.013), but no difference was detected between massage and placebo. Patient report of perceived clinical change was greater reduction in HA pain for massage than placebo or wait-list groups (p = 0.002)”. | Massage group—baseline 3.72 ± 0.23, after 3 weeks of treatment 3.38± 0.31, after 6 weeks of treatment 2.37 ± 0.36, p = 0.0003 *; Placebo group—baseline 3.81 ± 0.21, after 3 weeks of treatment 3.21 ± 0.29, after 6 weeks of treatment 2.92 ± 0.34, p = 0.013 *; Wait-list group—baseline 3.69 ± 0.21, after 3 weeks of treatment 3.54 ± 0.29, after 6 weeks of treatment 3.67 ± 0.33, p = 0.098. p-value between massage group and placebo group = 0.26 Group × Time Interaction = 0.026 * | Massage group—baseline 31.4 ± 2.69, after 3 weeks of treatment 26.3 ± 2.50, after 6 weeks of treatment 27.3 ± 3.04; Placebo group—baseline 33.3 ± 2.52, after 3 weeks of treatment 30.8 ± 2.34, after 6 weeks of treatment 29.8 ± 2.82; Wait-list group—baseline 31.2 ± 2.46, after 3 weeks of treatment 27.8 ± 2.28, after 6 weeks of treatment 29.5 ± 2.75. “No significant treatment group differences weredetected for HA intensity” Group × Time Interaction = 0.03 | Massage group—baseline 3.15 ± 0.43, after 3 weeks of treatment 3.20 ± 0.55, after 6 weeks of treatment 2.81 ± 0.50; Placebo group—baseline 2.86 ± 0.40, after 3 weeks of treatment 2.70 ± 0.52, after 6 weeks of treatment 2.84 ± 0.46; Wait-list group—baseline 3.02 ± 0.39, after 3 weeks of treatment 3.53 ± 0.51, after 6 weeks of treatment 3.36 ± 0.45 [hours]. “No significant treatment group differences were detected for HA duration” Group × Time Interaction = 0.49 | PPT—There was a significant time by treatment interaction for all the 4 sites tested (upper trapezius, left and right and suboccipital, left and right) (F values ranged from 4.49 to 7.91, p values ranged from <0.001 to 0.015). Post hoc analyses showed that scores ignificantly improved in the massage group (p values ranged from <0.001 to 0.002 across outcomes), but did not change in the placebo and wait-list groups (all Ps > 0.17). Quality of life—Post hoc tests showed a significant decrease in HDI scores in the intervention group (p = 0.0003) but not in the placebo (p = 0.06) or wait-list (p = 0.39) groups. A significant change in HIT-6 scores was detected over time in both the intervention (p = 0.0002) and placebo (p = 0.011) groups but not in the wait-list group (p = 0.52). perceived clinical change—end of treatment: massage group—small negative change 7.7%, no change 0%, small positive change 7.7%, moderate positive change 46.2%, large positive change 38.5%; placebo—small negative change 5.6%, no change 16.7%, small positive change 27.8%, moderate positive change 33.3%, large positive change 16.7%; wait-list—small negative change 5.9%, no change 82.4%, small positive change 11.7.%, moderate positive change 0%, large positive change 0%, p < 0.0001. perceived clinical change—after follow-up: massage group—small negative change 7.1%, no change 7.1%, small positive change 21.4%, moderate positive change 28.6%, large positive change 35.7%; placebo—small negative change 0%, no change 42.1%, small positive change 21.0%, moderate positive change 21.0%, large positive change 15.8%; wait-list—small negative change 0%, no change 81.2%, small positive change 12.5%, moderate positive change 6.2%, large positive change 0%, p = 0.002. | 4 weeks after end of treatment; pain intensity: massage group 22.8 ± 3.03, placebo group 31.5 ± 2.80, wait-list group 29.0 ± 2.74 [VAS 0–100]; pain frequency: massage group 2.61 ± 0.35, placebo group 2.96 ± 0.33, wait-list group 3.19 ± 0.32 [days per week]; pain duration: massage group 2.65 ± 0.4, placebo group—3.01 ± 0.44; wait-list group 3.12 ± 0.43 [hours]. | |
von Stülpnagel et al., 2009 [31] | headache diary—frequency, intensity, duration | “The headache frequency had been reduced from more than 3 days per week to 1 day per week (67.7% improvement). The intensity had nearly diminished to 1.67 on the visual analog scale compared to 6.5 visual analog scale before treatment (74.3% improvement). The headache duration also improved significantly from 6 h/d before treatment to 1.36 h/d after treatment (77.3% improvement)”. | before treatment 3.1 (1.5–7); after treatment 1 (0–3) [day per week] 67.7% improvement | before treatment 6.5 (5.5–8.5); after treatment 1.67 (0–4) [VAS 0–10] 74.3% improvement | before treatment 6 (1.5–12); after treatment 1.36 (0–2.5) [hours per day] 77.3% improvement | ND | - | no side effects |
Abaschian et al., 2020 [23] | Berggreen, Wiik and Lund, 2011 [24] | Gildir et al., 2019 [25] | Kamali et al., 2019 [26] | Mohamadi, Ghanbari, Rahimi Jaberi 2012 [27] | Mohamadi et al., 2020 [28] | Moraska, Chandler, 2008 [29] | Moraska et al., 2015 [30] | von Stülpnagel et al., 2009 [31] | |
---|---|---|---|---|---|---|---|---|---|
Eligibility criteria were specified (without points) | Y | Y | Y | N | - | Y | - | Y | - |
Subjects were randomly allocated to groups | 1 | 1 | 1 | 1 | - | 1 | - | 1 | - |
Allocation was concealed | 1 | 0 | 1 | 1 | - | 1 | - | 1 | - |
The groups were similar at baseline regarding the most important prognostic indicators | 0 | 1 | 1 | 1 | - | 1 | - | 1 | - |
There was blinding of all subjects | 1 | 0 | 1 | 1 | - | 0 | - | 0 | - |
There was blinding of all therapists who administered the therapy | 0 | 0 | 1 | 0 | - | 0 | - | 0 | - |
There was blinding of all assessors who measured at least one key outcome | 0 | 0 | 1 | 0 | - | 0 | - | 0 | - |
Measures of at least one key outcome were obtained from more than 85% of the subjects initially allocated to groups | 1 | 1 | 1 | 1 | - | 0 | - | 1 | - |
All subjects for whom outcome measures were available received the treatment or control condition as allocated | 0 | 1 | 0 | 0 | - | 1 | - | 0 | - |
The result of between-group comparisons are reported for at least one key outcome | 1 | 1 | 1 | 1 | - | 1 | - | 1 | - |
The study provides both point measures and measures of variability for at least one key outcome | 1 | 1 | 1 | 1 | - | 1 | - | 1 | - |
Total PEDro score | 6 | 6 | 9 | 7 | - | 6 | - | 6 | - |
Level of Evidence | 2b | 2b | 1b | 2b | 4 | 2b | 4 | 2b | 4 |
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Dolina, A.; Baszczowski, M.; Wilkowicz, W.; Zieliński, G.; Szkutnik, J.; Gawda, P. Trigger Point Therapy Techniques as an Effective Unconventional Method of Treating Tension Headaches: A Systematic Review. Healthcare 2024, 12, 1868. https://doi.org/10.3390/healthcare12181868
Dolina A, Baszczowski M, Wilkowicz W, Zieliński G, Szkutnik J, Gawda P. Trigger Point Therapy Techniques as an Effective Unconventional Method of Treating Tension Headaches: A Systematic Review. Healthcare. 2024; 12(18):1868. https://doi.org/10.3390/healthcare12181868
Chicago/Turabian StyleDolina, Aleksandra, Michał Baszczowski, Wiktor Wilkowicz, Grzegorz Zieliński, Jacek Szkutnik, and Piotr Gawda. 2024. "Trigger Point Therapy Techniques as an Effective Unconventional Method of Treating Tension Headaches: A Systematic Review" Healthcare 12, no. 18: 1868. https://doi.org/10.3390/healthcare12181868
APA StyleDolina, A., Baszczowski, M., Wilkowicz, W., Zieliński, G., Szkutnik, J., & Gawda, P. (2024). Trigger Point Therapy Techniques as an Effective Unconventional Method of Treating Tension Headaches: A Systematic Review. Healthcare, 12(18), 1868. https://doi.org/10.3390/healthcare12181868