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Clinical Trials/NCT05779878
NCT05779878RecruitingNot Applicable

Comparative Effects of Myofascial Arm Pull Technique and Post Isometric Relaxation on Pain, Range of Motion and Functional Disability in Adhesive Capsulitis After Mastectomy

Sahreen Anwar1 site in 1 country40 target enrollmentStarted: March 9, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
Range of motion in all planes

Study Overview

Brief Summary

Adhesive capsulitis (AC) also known as frozen shoulder typically manifests to decrease range of motion (ROM) and function and increase pain in shoulder .Objective of the study is To compare the effects of Myofascial Arm Pull Technique and Post-isometric Relaxation on Pain, Range of Motion and functional disability in adhesive capsulitis after mastectomy. The study design will be a Randomized Clinical Trial that will be used to compare the effects of Myofascial arm pull technique with post isometric relaxation. Subject with adhesive capsulitis meeting the predetermined inclusion & exclusion criteria will be divided into two groups. Pre assessment will be done using numeric pain rating scale NPRS for pain , shoulder pain and disability index (SPADI) tool for disability and Goniometer for Range of motion. Consent will be taken from patients by consent form the patients. They will be divided into two groups randomly by Random Number Generator table: Group A and Group B. For common treatment, both the groups will receive Ultrasound with a dosage of 1 MHz in frequency, continuous mode and 1.5 W/ cm2 of intensity for 10 minutes of treatment duration and Movement with mobilization will be applied for 15 times in 3 sets, and a 1- minute rest period was provided between each set. Group A will be given Post isometric relaxation technique with ultrasonic therapy. Group B will be given myofascial arm pull technique with ultrasonic. Total intervention protocol will be given for four weeks of duration 3 sessions per week with total 12 sessions. In Post isometric relaxation technique the therapist will slowly provide resistance in the direction of flexion, abduction, or external rotation, and without the subject intending to move for 15 minutes/ day, 3 times/week for 12 weeks. Similarly, myofascial arm pull technique the therapist will hold arm of the subject firmly and initial stretch will be applied in abduction and external rotation for 8-10 times in each session per day for 3 days/week for 4 weeks. Outcome measures will be measured at baseline, after 2 weeks and after 4 weeks. Data analysis will be done by SPSS version 25.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
25 Years to 50 Years (Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Only Female gender
  • •Age between 25 to 50 years with post mastectomy.
  • •Diagnosis of breast cancer (grade 1to3 b).
  • •Post mastectomy state at least 6 months.
  • •Shoulder pain that began after the breast cancer surgery

Exclusion Criteria

  • •Bilateral breast cancer.
  • •History of neurologic deficits affecting shoulder functioning during daily activites.
  • •On numeric pain rating scale pain will be less than 5.

Arms & Interventions

Interventional Group A

Experimental

This group will be given Post isometric relaxation technique. Total intervention protocol will be given for four weeks of duration 3 sessions per week with total 12 sessions.

Intervention: Post Isometric Relaxation (Other)

Interventional Group B

Experimental

This Group will be given myofascial arm pull technique . Total intervention protocol will be given for four weeks of duration 3 sessions per week with total 12 sessions.

Intervention: Myofascial arm pull technique (Other)

Outcomes

Primary Outcomes

Range of motion in all planes

Time Frame: 4 weeks

Range of motions in all planes will be measured by using goniometer

Pain in Shoulder Joint

Time Frame: 4 weeks

Pain will be measured by using Numeric pain rating scale

Functional disability

Time Frame: 4 weeks

Functional disability will be measured by using Shoulder Pain and Disability Index

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Sahreen Anwar
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Sahreen Anwar

Dr

Riphah International University

Study Sites (1)

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