Comparative Effects of the Bowen Technique With and Without Extracorporeal Shock Wave Therapy in Patients With Deep Gluteal Syndrome
Bowen+ESWT
1 other identifier
interventional
46
1 country
1
Brief Summary
A single-blinded, randomized controlled trial consisting of 46 participants with Deep Gluteal syndrome, calculated by the G power tool with an attrition rate of 5 % will be conducted. Participants will be recruited using non-probability convenience sampling based on pre-defined inclusion and exclusion criteria. Participants will be randomly assigned into two groups with 23 participants each group. Group A will receive Bowen Technique with extracorporeal shockwave therapy. Group B will receive Bowen Technique without extracorporeal shockwave therapy in conjunction with conventional therapy. Primary outcomes like pain, functional level and ROM will be measured at baseline and post-intervention using the Lower extremity functional scale (LEFS), Numeric Pain Rating scale (NPRS), and Goniometer. Data will be analyzed by IBM SPSS 26.0 with the Shapiro-Wilk test to confirm the normality.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started May 2026
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 25, 2026
CompletedFirst Submitted
Initial submission to the registry
August 10, 2026
CompletedFirst Posted
Study publicly available on registry
August 19, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
CompletedAugust 21, 2026
August 1, 2026
2 months
August 10, 2026
August 19, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
UNIVERSAL GONIOMETRY
A goniometer is a conventional clinical tool utilized to assess joint range of motion (ROM), offering objective and dependable measurements to assess mobility restrictions in musculoskeletal disorders72 . Goniometric measurement of passive hip ROM has good test-retest reliability, with ICC ranging from 0.82 to 0.94 across different hip movements79 * For goniometric evaluation of hip internal rotation, the minimal detectable change (MDC) is 8.6°, and for hip external rotation, it is 6.1° 18 * According to anchor-based methodology, the minimal clinically significant difference (MCID) for hip range of motion is 5.81° 80
6 Weeks
NUMERICAL PAIN RATING SCALE (NPRS)
The Numeric Pain Rating Scale (NPRS) is a self-reported metric utilized to evaluate pain severity in individuals with musculoskeletal conditions 70 * It is a simple 11-point scale that ranges from 0 (no pain) to 10 (worst pain imaginable) that can be administered verbally or in writing 74 * which shows multilevel likelihood ratios of 0.99 (scores 1-3), 2.67 (scores 4-6), and 5.60 (scores 7-10) for detecting pain-related functional interference, and an established sensitivity of 69 percent at ascore of 175 .Patients are asked to rate their current, best, and worst pain levels during the previous 24 hours, and the average of the three values is used to get the final pain intensity score 76 The NPRS minimal clinically significant difference (MCID) in this current study was set at two points 77 . The NPRS is widely used in research and clinical environments due to its ease of use, high reliability, validity, and responsiveness to clinically relevant changes in both acute and chronic
6 Weeks
Secondary Outcomes (1)
LEFS
6 Weeks
Study Arms (2)
GROUP A (Bowen Technique with ESWT)
EXPERIMENTALGroup A will receive Bowen Technqiue with ESWT along with conventional Physiotherapy Protocol.
GROUP B (Bowen technique without ESWT)
ACTIVE COMPARATORGroup B will receive Bowen Technqiue ONLY along with conventional Physiotherapy Protocol.
Interventions
Bowen Technique is a gentle manual fascial technique used to reduce muscle tension, pain, and soft-tissue restriction. ESWT is a non-invasive mechanical treatment that delivers shockwaves to promote analgesia, circulation, and tissue repair. In Deep Gluteal Syndrome, both can target the painful and restricted deep gluteal tissues, so my study compares Bowen alone with Bowen combined with ESWT to determine whether the addition of ESWT provides greater clinical benefit
The Bowen Technique is a gentle manual soft-tissue technique developed by Thomas Bowen. It uses slow, precise, cross-fiber rolling movements over muscles, tendons, ligaments, and fascia, with short rest periods between sets of movements. In your study, the therapist applies gentle pressure to the deep gluteal muscles, holds the tissue briefly, then moves across it in a controlled manner.
Eligibility Criteria
You may qualify if:
- Individuals aged 25 to 45 years, including both genders 55
- Positive FAIR, Active Piriformis Test, Seated Piriformis Stretch Test 56,6,57
- NPRS pain score ≥ 3/10 55
- For a minimum of four weeks, there has been unilateral discomfort in the buttock, with or without accompanying posterior thigh pain, exacerbated by sitting 58
You may not qualify if:
- Previous surgery involving the ipsilateral hip, pelvis, lumbar spine, or sacroiliac joint 34
- Women who were pregnant or nursing were excluded 59
- Medical conditions such as tumors or fractures 60
- Neuromuscular disorders that impair normal lumbopelvic morphology or progressive neurologic disease 60
- Disc pathologies identified through radiological imaging 17
- Pathologies of the hip joint and soft tissues 17
- Recent trauma history 17
- History of polyneuropathy, sciatic nerve injury, rheumatological disease, or malignancy 17
- Corticosteroid therapy or opioid-derived analgesia for pain during the previous month 17
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Management and technology Sialkot Campus
Sialkot, Punjab Province, 51070, Pakistan
Related Publications (4)
Amjad F, Khalid A. Comparative effects of Bowen therapy and tennis ball technique on pain and functional disability in patients with thoracic myofascial pain syndrome. J Orthop Surg Res. 2023 Nov 24;18(1):895. doi: 10.1186/s13018-023-04379-z.
PMID: 37996838RESULTDe la Corte-Rodriguez H, Roman-Belmonte JM, Rodriguez-Damiani BA, Vazquez-Sasot A, Rodriguez-Merchan EC. Extracorporeal Shock Wave Therapy for the Treatment of Musculoskeletal Pain: A Narrative Review. Healthcare (Basel). 2023 Oct 26;11(21):2830. doi: 10.3390/healthcare11212830.
PMID: 37957975RESULTKurkova S, Kyncl M, Ibrahim I, Lachman H, Sakmarova K, Machac S. Exploring non-invasive diagnostic tools for deep gluteal syndrome: a multimodal approach integrating clinical and imaging techniques. Quant Imaging Med Surg. 2025 Sep 1;15(9):8409-8422. doi: 10.21037/qims-2025-241. Epub 2025 Aug 13.
PMID: 40893505RESULTCarro LP, Hernando MF, Cerezal L, Navarro IS, Fernandez AA, Castillo AO. Deep gluteal space problems: piriformis syndrome, ischiofemoral impingement and sciatic nerve release. Muscles Ligaments Tendons J. 2016 Dec 21;6(3):384-396. doi: 10.11138/mltj/2016.6.3.384. eCollection 2016 Jul-Sep.
PMID: 28066745RESULT
Related Links
MeSH Terms
Conditions
Study Officials
- PRINCIPAL INVESTIGATOR
Hamza Zahid
University of Management and Technology Sialkot Pakistan
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- The study followed a single-blinded design in which the outcome assessors were masked to the participants' treatment allocation. Assessors were not informed whether a participant belonged to the Bowen Technique with ESWT group or the Bowen Technique without ESWT group. This helped reduce assessment and observer bias during pre- and post-treatment measurements. Participants were aware of the treatment they received, but the assessors remained blinded throughout outcome evaluation
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head of the department
Study Record Dates
First Submitted
August 10, 2026
First Posted
August 19, 2026
Study Start
May 1, 2026
Primary Completion
June 25, 2026
Study Completion
September 1, 2026
Last Updated
August 21, 2026
Record last verified: 2026-08