Myofascial Release and Positional Release Techniques in Unilateral Trapezitis
Effectiveness of Myofascial Release and Positional Release Techniques on Pain, Cervical Range of Motion, and Neck Disability in Patients With Unilateral Trapezitis
1 other identifier
interventional
30
1 country
1
Brief Summary
Unilateral trapezitis is characterized by upper trapezius myofascial pain and trigger points and commonly causes neck pain, restricted cervical range of motion (ROM), and functional disability. While myofascial release (MFR) and positional release technique (PRT) are widely used, their comparative effectiveness remains unclear. Therefore, this study aimed to compare the effectiveness of MFR versus PRT combined with conventional exercises on pain, cervical lateral flexion ROM, and neck disability in young adults with unilateral trapezitis. Thirty participants (aged 20-25 years) with unilateral trapezitis were randomly assigned to two groups (n=15 each). Group A received MFR plus conventional treatment (active neck movements, trapezius stretching), while Group B received PRT plus the same conventional treatment. Interventions were delivered 3 days/week for 20 minutes/session over 2 months. Outcomes included Numerical Pain Rating Scale (NPRS), goniometric cervical lateral flexion ROM (affected/unaffected sides), and Neck Disability Index (NDI), measured pre- and post-intervention. Both MFR and PRT effectively improved pain, ROM, and disability in unilateral trapezitis. PRT demonstrated greater short-term benefits for pain reduction and functional improvement, suggesting it as the preferred initial intervention when rapid symptomatic relief is prioritized.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Sep 2023
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
September 5, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 14, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
May 20, 2024
CompletedFirst Submitted
Initial submission to the registry
March 31, 2026
CompletedFirst Posted
Study publicly available on registry
April 7, 2026
CompletedAugust 7, 2026
August 1, 2026
6 months
March 31, 2026
August 4, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Neck Pain
Pain on the affected side was measured using the Numerical Pain Rating Scale. The Numerical Pain Rating Scale-11 is a widely used 11-point scale for self-reporting pain. The respondent chooses a whole number (0-10) that best reflects the intensity of their pain. The greater the number, the worse is the outcome.
8 weeks.
Secondary Outcomes (2)
Range of motion
8 weeks.
Functional status
8 weeks.
Study Arms (2)
Experimental Group 1
EXPERIMENTALIn this group, participants received the myofascial release technique and conventional treatment, including active neck movements and trapezius stretching.
Experimental Group 2
ACTIVE COMPARATORIn this group, participants received the positional release technique and conventional treatment, including active neck movements and trapezius stretching.
Interventions
Myofascial release technique is a specialized manual therapy technique used to alleviate chronic pain and restore motion by releasing tension in the fascia.
The Positional Release Technique is a gentle manual therapy that resolves pain and tissue dysfunction by moving the body into a "position of ease" or comfort.
Eligibility Criteria
You may qualify if:
- Subjects diagnosed with trapezitis with trigger point by an orthopedic surgeon,
- with unilateral upper trapezius tender point,
- taut band palpable in upper trapezius muscle,
- excruciating spot tenderness at one point along the length of the taut band of upper trapezius muscle,
- restriction in cervical lateral flexion when measured, and
- pain elevated by elongating (stretching) the trapezius muscle
You may not qualify if:
- Participants with history of cervical spine trauma or fracture,
- recent surgery on the cervical spine,
- skin condition around area to be treated,
- current use of anti-inflammatory medications,
- brachial nerve pain,
- deformities of the neck,
- sensory/perception anomalies close to the treatment area,
- radiculopathy or myopathy symptoms,
- degenerative cervical spine condition,
- with a history of cardiac illness or presence of a pacemaker,
- epilepsy,
- psychological disorder, and
- pregnant women
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- King Saud Universitylead
- Cooperative Institute of Health Sciencescollaborator
Study Sites (1)
Co-Operative Institute of Health Sciences
Kannur, Kerala, 670105, India
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 31, 2026
First Posted
April 7, 2026
Study Start
September 5, 2023
Primary Completion
March 14, 2024
Study Completion
May 20, 2024
Last Updated
August 7, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share