To Compare the Efficacy of Instrument Assisted STM vs BT in Alleviating Pain and Tightness of Trapezius Muscle

NCT ID: NCT07037147

Last Updated: 2025-06-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

26 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-03-04

Study Completion Date

2025-09-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Trapezius muscle pain and tightness are common musculoskeletal issues that can significantly impair movement and quality of life. Instrument Assisted Soft Tissue Mobilization (IASTM) and Bowen Therapy are gaining attention as non-invasive treatments for myofascial pain and tension.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

It will be single blinded randomized clinical trial (RCT). The study will be conducted on 26 participants which will be categorized into two groups. Group one will be given IASTM and group two will receive Bowen technique. Non-probability convenience sampling technique will be used for data collection at physiotherapy department at Fatima memorial hospital followed by lottery method of allocation of groups. Data will be collected by using visual analogue scale, goniometer and neck disability index.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Trapezius Muscle Strain

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

instrument assistance soft tissue mobilisation

Group Type EXPERIMENTAL

instrument assistance soft tissue mobilisation

Intervention Type COMBINATION_PRODUCT

In this group instrument assistance soft tissue mobilisation will be given followed by conventional therapy. IASTM will be given by using IASTM tool M2T blade. In this process patient will be asked to sit in a chair by resting its forearm in front of the table.

Bowen technique

Group Type EXPERIMENTAL

Bowen technique

Intervention Type COMBINATION_PRODUCT

In this group Bowen technique will be given after the basic conventional therapy. For this technique patient will be asked to lie in a prone position where the neck of the patient will be supported with the help of a small pillow. Therapist thumb will be placed on the affected side of the muscle.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

instrument assistance soft tissue mobilisation

In this group instrument assistance soft tissue mobilisation will be given followed by conventional therapy. IASTM will be given by using IASTM tool M2T blade. In this process patient will be asked to sit in a chair by resting its forearm in front of the table.

Intervention Type COMBINATION_PRODUCT

Bowen technique

In this group Bowen technique will be given after the basic conventional therapy. For this technique patient will be asked to lie in a prone position where the neck of the patient will be supported with the help of a small pillow. Therapist thumb will be placed on the affected side of the muscle.

Intervention Type COMBINATION_PRODUCT

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age from 18 to 50 years
* Both gender
* Bilateral trapezius muscle tightness assessed by palpation.
* Subject with the presence of myofacial trigger points in upper trapezius muscle assessed on palpation.
* Patient with symptoms for the past two weeks.
* People with pain of neck due to tight muscle more than 3 on VAS.

Exclusion Criteria

* Participant with any fracture of cervical spine or surgery within the 6 month timespan.
* Participant with radiating neck pain towards the upper extremity.
* People with other conditions like disc prolapse, spondylolisthesis, tb of spine etc.
* People with any instrument assistance soft tissue mobilisation technique contraindication.
* People with whiplash injury history.
* Participant who has been diagnosed with myopathy or fibromyalgia.
* Pregnant females who has already gone under myofacial therapy within the past month.
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Superior University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Muhammad Naveed Babur

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Fatima Memorial Hospital

Lahore, , Pakistan

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Pakistan

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

DPT/Batch-Fall20/1007

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Comparison of Two Treatments on Nonspecific Neck Pain
NCT06485921 ACTIVE_NOT_RECRUITING NA