- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07602972
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
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.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Tension neck syndrome is a common musculoskeletal condition characterized by neck pain, muscle tightness, and limited cervical range of motion. Manual therapy interventions such as Graston Technique and Manual Soft Tissue Release are widely used in physiotherapy practice, but direct comparative evidence between them is limited.
This interventional study aims to compare the effects of Graston Technique versus Manual Soft Tissue Release on pain intensity and cervical range of motion in patients diagnosed with tension neck syndrome.
Participants will be randomly assigned to one of two intervention groups. Group 1 will receive Graston Technique, and Group 2 will receive Manual Soft Tissue Release. Both interventions will be delivered by qualified physiotherapists according to a standardized protocol. Outcomes including pain, measured by the Numeric Pain Rating Scale, and cervical range of motion, measured by goniometry, will be assessed at baseline and post-intervention.
The study will help determine which technique provides greater improvement in pain reduction and functional mobility, guiding clinical decision-making in the management of tension neck syndrome.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab Province
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Lahore, Punjab Province, Pakistan, 54000
- Rafique Bhatti Memorial Hospital, Department of Physiotherapy
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- 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.
Exclusion Criteria:
- 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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Graston Technique
Participants 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.
|
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.
Other Names:
|
|
Experimental: Manual Soft Tissue Release
Participants 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.
|
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.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Neck Pain Intensity
Time Frame: Baseline and after 12 weeks of intervention
|
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
Time Frame: Baseline and after 12 weeks of intervention
|
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
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Wajeeha Nadeem, Masters in Rehabilitation Scie, Green Internation University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- GIU/REC/26-36
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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