Effect of Active Release Technique and Abdominal Drawing-Maneuver on Pain and Quality of Life in Patients With Chronic Low Back Pain

May 23, 2022 updated by: Muhammad Naveed Babur, Superior University
To determine the effect of active release technique and abdominal drawing in maneuver on pain and quality of life in patients of chronic low back pain.

Study Overview

Status

Enrolling by invitation

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

23

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

  • Pakistan
      • Lahore, Pakistan
        • Ibrahim PT Clinic Lahore Zohaib Physiotherapy Clinic, Farooq Abad

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

20 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patient with hamstring tightness[9]
  • Subjects with pain between 4 and 7cm on visual analogue scale[18].
  • Subjects having 20-40 age group are included in this study[11]
  • Patients having pain for more than 3 month of mild-moderate intensity[9]

Exclusion Criteria:

  • Patients with any spine injury[11]
  • Lumber intervertebral disc fracture[11]
  • Patients having any surgical history of spine[11]
  • Spinal stenosis[11]

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: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Active Release Technique
Using Active Release Technique
Diagnostic test: Active Release Technique
Using Active Release Technique
Experimental: Abdominal Drawing-Maneuver
Using Abdominal Drawing-Maneuver Technique
Diagnostic test: Abdominal Drawing-Maneuver
Using Abdominal Drawing-Maneuver Technique

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Abdominal Drawing-Maneuver on Pain and Quality of Life in Patients With Chronic Low Back Pain
Time Frame: 6 Months
11 participents with The Hot pack initially for 10 minutes then this group will receive abdominal drawing-in maneuver technique for 2 times in week of 10 session. SF-36 Questionnaire.
6 Months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Active Release Technique in Patients With Chronic Low Back Pain
Time Frame: 6 Months
12 participents with The Hot pack initially for 10 minthen this group will receive active release technique 2 times in week of 10 session while other group will receive abdominal drawing-in maneuver technique for 2 times in week of 10 session. Visual analogue scale.
6 Months

Collaborators and Investigators

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

Sponsor

Superior University

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)

March 31, 2022

Primary Completion (Anticipated)

June 1, 2022

Study Completion (Anticipated)

September 1, 2022

Study Registration Dates

First Submitted

May 9, 2022

First Submitted That Met QC Criteria

May 23, 2022

First Posted (Actual)

May 27, 2022

Study Record Updates

Last Update Posted (Actual)

May 27, 2022

Last Update Submitted That Met QC Criteria

May 23, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • DPT/Batch-Fall17/518

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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