Comparative Effect of ART and MET on Pain, ROM and Functional Disability in AC Patients With Trigger Points

July 2, 2022 updated by: University of Lahore

Comparative Effect of Active Release Technique and Muscles Energy Technique on Pain, ROM and Functional Disability in Adhesive Capsulitis Patients With Trigger Points

The aim of this study to determine the Comparative effect of active release technique and muscle energy technique on pain, ROM and functional disability in adhesive capsulitis patients with trigger points.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

Detailed Description

74 participants are included in this study in two groups and 37 for each group. Group A for active release technique along with conventional therapy and Group B for muscles energy technique along with conventional therapy.

Study Type

Interventional

Enrollment (Anticipated)

74

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

40 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Both male and female.
  • Participants having unilateral adhesive capsulitis.
  • Participants with sub-acute adhesive capsulitis.
  • Participants having age of 40-60 years.

Exclusion Criteria:

  • Patient with cervical radiculopathy.
  • Fractures of upper limb.
  • Thoracic outlet syndrome.
  • Post-traumatic.

Study Plan

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

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Active Release Technique
In ART the particular muscle is taken from shortened to lengthened position or vice versa. Duration of treatment will be of 8-15min
Other: Active Release Technique and muscle energy technique
74 participants divided into two groups and 37 in each group.
Experimental: Muscles Energy Technique
In METs,the protocol will perform for 3 repetitions per day and thrice a week for 5 week.
Other: Active Release Technique and muscle energy technique
74 participants divided into two groups and 37 in each group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numerical pain rating scale
Time Frame: Change from Baseline in pain to 6 week
patients rate their pain from 0 to 10, from 0 to 20, or from 0 to 100. Zero represents "no pain," whereas 10, 20, or 100 represents the opposite end of the pain continuum (e.g., "the most intense pain imaginable," "pain as intense as it could be," "maximum pain").
Change from Baseline in pain to 6 week
Universal Goniometry
Time Frame: Change from Baseline in range of motion to 6 week
Universal goniometer (UG) is commonly used as a standard method to evaluate range of motion (ROM) as part of joint motions.
Change from Baseline in range of motion to 6 week
Shoulder Pain and Functional Disability Index
Time Frame: Change from Baseline in disability to 6 week
The Shoulder Pain and Disability Index (SPADI) is a self-administered questionnaire consisting of items grouped into pain and disability subscales.
Change from Baseline in disability to 6 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University of Lahore

Investigators

  • Study Chair: Shahzadi Sumbal Naz, Dpt, UOL

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 10, 2022

Primary Completion (Actual)

February 25, 2022

Study Completion (Anticipated)

September 30, 2022

Study Registration Dates

First Submitted

May 22, 2022

First Submitted That Met QC Criteria

July 2, 2022

First Posted (Actual)

July 7, 2022

Study Record Updates

Last Update Posted (Actual)

July 7, 2022

Last Update Submitted That Met QC Criteria

July 2, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC-UOL-/98-04/2022

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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