Comparison of Active Release Technique and Bent Leg Raise In Osteoarthritis.

September 17, 2021 updated by: Riphah International University

Comparison Of Effects Of Active Release Technique And Bent Leg Raise On Hamstring Flexibility In Patients With Knee Osteoarthritis

The objective of the study was to compare the effects of active release technique and bent leg raise on hamstring flexibility, functional outcomes, and pain in patients with knee osteoarthritis.

Study Overview

Status

Completed

Conditions

Detailed Description

Knee Osteoarthritis is a common progressive degenerative joint disease. Muscular weakness and other structural abnormalities can cause low back pain. Hamstring muscle being a postural muscle has an increased tendency to become tight. In this study, participants with knee osteoarthritis having hamstring tightness were included. Active Release Technique and Bent Leg Raise technique have been used to increase flexibility in hamstrings in these patients with knee osteoarthritis.

Study Type

Interventional

Enrollment (Actual)

48

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

    • Federal
      • Islamabad, Federal, Pakistan, 44000
        • Noor Physio and Sports Injury Clinic, G-8 Markaz
    • Punjab
      • Rawalpindi, Punjab, Pakistan, 46000
        • Riphah Rehabilitation Center, Westridge campus, Potohar Tower, Peshawar Road

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

45 years to 60 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Diagnosed patients of Knee Osteoarthritis
  • Hamstring length less than 160 degrees
  • Minimum history of 3 months
  • Willing to participate

Exclusion Criteria:

  • Patients who have passive knee extension more than 160 degrees
  • Patients with less than 3 months history
  • Patients who have osteoarthritis of other than the knee joint
  • Patients with history of fracture
  • Patients with post surgical history

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
Hot pack, TENS, Quadriceps Isometric strengthening, Active Release Technique

Moist Hot pack 10 mins/1 set/ (6 days/ week), TENS 20 mins/1 set/ (6 days/ week), Quadriceps Isometric Strengthening 5 sec hold, 10 reps/ 1 set/(6 days/ week), Active release Technique 5 reps/ 1 set/ (6 days/ week)

A total of 2 weeks (12 sessions, 6 sessions/ week) were given each consisting of 40 mins.

Active Comparator: Bent leg raise
Hot pack, TENS, Quadriceps Isometric strengthening, Bent leg raise

Moist Hot pack 10 mins/1 set/ (6 days/ week), TENS 20 mins/1 set/ (6 days/ week), Quadriceps Isometric Strengthening 5 sec hold, 10 reps/ 1 set/(6 days/ week), Bent leg raise 5 sec hold/ 5 sec stretch/ 3 reps/ 1 min rest interval/ 1 set/ (6 days/ week).

A total of 2 weeks (12 sessions, 6 sessions/ week) were given each consisting of 40 mins.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hamstring flexibility
Time Frame: 12 days
Changes from baseline, Hamstring flexibility was measured through passive knee extension test with the help of Goniometer. Normal value of knee extension angle is 180 degrees. Values decreased than 160 degree represents hamstring tightness.
12 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Functional outcome
Time Frame: 12 days
Changes from baseline, Functional outcome was taken through western Ontario McMaster Universities Osteoarthritis Index tool. It comprises three sections containing 24 items. Score ranges from 0 to 96. 0 representing a healthy state and higher scores indicating worst health.
12 days
Pain on Visual analogue Scale
Time Frame: 12 days
Changes from baseline, Pain was measured through Visual Analogue Scale. It comprises of a continuous scale of 10cm line. 0 to 4mm represents "no pain", 5mm to 44mm indicates "mild pain", whereas 45mm to 74mm indicates "moderate pain" and continues to the range of "worst pain" between 75mm to 100 mm.
12 days

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Asghar Khan, PhD, Riphah International 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)

November 14, 2020

Primary Completion (Actual)

April 20, 2021

Study Completion (Actual)

April 30, 2021

Study Registration Dates

First Submitted

August 23, 2021

First Submitted That Met QC Criteria

September 17, 2021

First Posted (Actual)

September 27, 2021

Study Record Updates

Last Update Posted (Actual)

September 27, 2021

Last Update Submitted That Met QC Criteria

September 17, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

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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