Completed

Muscle Energy Technique vs. Modified Active Release Technique for Scapulocostal Syndrome: Impact on Pain, Chest Expansion, and Functional Disability

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Study Aim

This study aims to compare the effectiveness of two treatment techniques, Muscle Energy Technique and Modified Active Release Technique, on reducing pain, improving chest expansion, and decreasing functional disability in individuals with Scapulocostal Syndrome.

What is being tested

Muscle Energy Technique

+ Conventional Physical Therapy

+ Modified Active Release Technique

Other
Who is being recruted

Neurologic Manifestations+2

+ Pain

+ Signs and Symptoms

From 18 to 40 Years
+16 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: January 2025
See protocol details

Summary

Principal SponsorRiphah International University
Last updated: February 12, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: January 10, 2025

Actual date on which the first participant was enrolled.

This study focuses on comparing the effects of two techniques, Muscle Energy Technique and Modified Active Release Technique, in helping patients with Scapulocostal Syndrome, a condition that affects the shoulder and chest area. The main goal is to see how these techniques impact pain, chest expansion, and functional disability in these patients. This research is crucial as it could help improve treatment options for individuals dealing with this condition. During the study, participants undergo measurements using a simple measuring tape to assess chest expansion at different points of breathing. The study also uses the Neck Disability Index, a questionnaire about daily activities, to evaluate how the condition affects the patient's daily life. Additionally, the Numeric Pain Rating Scale is used to measure the severity of pain, with scores ranging from 0 (no pain) to 10 (severe pain). These tools help the researchers determine the effectiveness of the two techniques in managing pain and improving functionality.

Official TitleComparative Effects of Muscle Energy Technique and Modified Active Release Technique in Patients With Scapulocostal Syndrome.
Principal SponsorRiphah International University
Last updated: February 12, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

46 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 40 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neurologic ManifestationsPainSigns and SymptomsPathological Conditions, Signs and SymptomsNeck Pain

Criteria

7 inclusion criteria required to participate
NPRS value> than 3.

Pain duration should be present for at least for 3 months before inclusion in the study.

Chest expansion value < than 3cm are included.

Age between 18-40 yrs.

Show More Criteria

9 exclusion criteria prevent from participating
Brachial neuralgia.

Cervical Radiculopathy.

Thoracic outlet syndrome.

Past Surgical Area.

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental

Group II

Active Comparator

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

AAHAD Hospital Sialkot.

Sialkot, PakistanOpen AAHAD Hospital Sialkot. in Google Maps
CompletedOne Study Center