Effects of Graston Technique Versus Soft Tissue Release on Neck Pain and Range of Motion.
GT vs MSTR
Comparative Effects of Graston Technique and Manual Soft Tissue Release on Pain and Range of Motion in Patients With Tension Neck Syndrome
1 other identifier
interventional
40
1 country
1
Brief Summary
This study compares two manual therapy techniques for treating tension neck syndrome: Graston Technique and Manual Soft Tissue Release. Tension neck syndrome causes neck pain, stiffness, and reduced range of motion. Participants will be assigned to receive either Graston Technique or Manual Soft Tissue Release for a set number of sessions. Researchers will measure changes in neck pain and range of motion before and after treatment to see which technique is more effective. The purpose is to provide evidence on the best manual therapy approach for improving neck pain and movement in patients with tension neck syndrome.
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 Nov 2025
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
November 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 29, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 5, 2026
CompletedFirst Submitted
Initial submission to the registry
May 16, 2026
CompletedFirst Posted
Study publicly available on registry
May 22, 2026
CompletedMay 22, 2026
May 1, 2026
6 months
May 16, 2026
May 16, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Change in Neck Pain Intensity
Neck pain intensity measured using the Numeric Pain Rating Scale (NPRS), where 0 = no pain and 10 = worst pain imaginable. Higher scores indicate greater pain.
Baseline and after 12 weeks of intervention
Change in Cervical Range of Motion
Cervical range of motion for flexion, extension, lateral flexion, and rotation measured in degrees using a goniometer. Higher values indicate greater range of motion.
Baseline and after 12 weeks of intervention
Study Arms (2)
Graston Technique
EXPERIMENTALParticipants in this arm receive Graston Technique, an instrument-assisted soft tissue mobilization therapy. Treatment is applied to the cervical spine and upper trapezius muscles using stainless steel instruments. Frequency and duration of sessions are as defined in the study protocol. All interventions are delivered by a licensed physiotherapist.
Manual Soft Tissue Release
EXPERIMENTALParticipants in this arm receive Manual Soft Tissue Release, a hands-on manual therapy technique. The therapist applies sustained pressure and stretching to release tightness in the cervical spine and upper trapezius muscles. Frequency and duration of sessions are as defined in the study protocol. All interventions are delivered by a licensed physiotherapist.
Interventions
Instrument-assisted soft tissue mobilization using stainless steel Graston Technique instruments. The technique is applied to the cervical spine and upper trapezius muscles to reduce pain and improve range of motion in patients with tension neck syndrome. Treatment is delivered by a licensed physiotherapist according to the study protocol.
Manual soft tissue mobilization technique performed by a licensed physiotherapist using hands-on pressure and stretching. The technique targets tightness in the cervical spine and upper trapezius muscles to reduce pain and improve cervical range of motion in patients with tension neck syndrome. Treatment is delivered according to the study protocol.
Eligibility Criteria
You may qualify if:
- Patients aged 20-60 years.
- Patients of both genders.
- Patients with persistent neck pain.
- Patients with neck pain absent of spondylosis, disk prolapse, or radiculopathy.
You may not qualify if:
- The patients who did not want to participate
- The patients who just had cervical spine surgery.
- The patients who had recent cervical injury.
- The patients who comes with tumor of the cervical spine.
- The patients affected by neck dysfunction.
- The patients with cervical disc herniation.
- The patients who had difficulties in language.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Rafique Bhatti Memorial Hospital, Department of Physiotherapy
Lahore, Punjab Province, 54000, Pakistan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Wajeeha Nadeem, Masters in Rehabilitation Scie
Green Internation University
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
May 16, 2026
First Posted
May 22, 2026
Study Start
November 2, 2025
Primary Completion
April 29, 2026
Study Completion
May 5, 2026
Last Updated
May 22, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR
- Time Frame
- It will be available after the completion of the study.
- Access Criteria
- De-identified individual participant data and the study protocol will be made available to researchers whose proposed use of the data has been approved by the study team. Requests should be sent to the corresponding author via email. Data will be shared after execution of a data use agreement and for the purpose of meta-analysis or secondary research related to tension neck syndrome and manual therapy.
Only IPD used in the results publication will be shared