Effects of Hip Abductors Strengthening In Knee Osteoarthritis

March 8, 2022 updated by: Riphah International University

Comparison of Hip Abductors and Quadriceps Strengthening With Quadriceps Strengthening Alone in Knee Osteoarthritis

The aim of my study is to determine the effects of hip abductors strengthening and quadriceps strengthening in comparison with quadriceps strengthening alone in patients with knee osteoarthritis.

Study Overview

Detailed Description

As the quadriceps strengthening is a keystone of exercise therapy for knee osteoarthritis. Thus is the hip abductors strengthening along with quadriceps strengthening would be added to the treatment protocol of osteoarthritis it might give more positive results, decrease pain and increase the recovery rate as well as helpful to improve the functional outcomes.

Study Type

Interventional

Enrollment (Actual)

40

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

    • Khyber Pakhtunkhwa
      • Mansehra, Khyber Pakhtunkhwa, Pakistan, 21300
        • Khattak Physiotherapy and Rehabilitation Center

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

50 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Osteoarthritis of single or both knees
  • Kellgren Lawrence scale between 2-4

Exclusion Criteria:

  • Knee valgus or varus deformity
  • Hip or knee joint replacement
  • Tibial osteotomy
  • Any other surgery of hip or knee joint

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: Hip Abductor Strengthening
This group received quadriceps and hip abductor strengthening along with patellar mobilization and stretching exercises.

Elastic resisted training of Hip Abductors (5-10 seconds hold) 10 repetitions x 3 sets, 3 alternate days per week.

Elastic resisted training of Quadriceps (5-7 seconds hold) 10 repetitions x 3 sets, 3 alternate days per week.

Static Stretching of 5 seconds hold (Calf, Hamstrings, Gluteal muscles and Iliotibial band) 10 repetitions x 3 sets, 3 alternate days per week.

Patellar Mobilization in all four directions 10 repetitions x 3 sets, 3 alternate days per week.

Total 18 sessions were given in 06 weeks.

Active Comparator: Traditional Physical Therapy
This group received quadriceps strengthening along with patellar mobilization and stretching exercises.

Elastic resisted training of Quadriceps (5-7 seconds hold) 10 repetitions x 3 sets, 3 alternate days per week.

Static Stretching of 5 seconds hold (Calf, Hamstrings, Gluteal muscles and Iliotibial band) 10 repetitions x 3 sets, 3 alternate days per week.

Patellar Mobilization in all four directions 10 repetitions x 3 sets, 3 alternate days per week.

Total 18 sessions were given in 06 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric Pain Rating Scale (NPRS)
Time Frame: 6 weeks
Changes from baseline- The Numeric Pain Rating Scale is a self-reported, or clinician administered, measurement tool consisting of a numerical point scale from 0-10 with extreme anchors of '0-no pain' to '10-extreme pain'. The scale ranges most commonly from 0-10 or 0-100, and can be administered in written or verbal form. 0 means " no pain" ands 10 or 100 means "Worst pain imaginable"
6 weeks
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
Time Frame: 6 weeks
Changes from baseline- The Western Ontario and McMaster Universities Osteoarthritis Index is a tested questionnaire to assess symptoms and physical functional disability in patients with Osteoarthritis of the knee and the hip. The function dimension explores the degree of difficulty in 17 activities. Its score ranges from 0-96. 0 represents the best health status and 96 the worst possible status
6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Five Times Sit to Stand Test (FTSST)
Time Frame: 6 weeks
Changes from baseline- Five time Sit-to-Stand Test was related to lower-extremity proprioception, postural sway, strength, and visual contrast sensitivity. Various methods have been used in an attempt to determine how well older adults can rise from a chair have suggested repeating the chair rise 5 times.
6 weeks

Collaborators and Investigators

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

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 1, 2021

Primary Completion (Actual)

January 15, 2021

Study Completion (Actual)

January 30, 2022

Study Registration Dates

First Submitted

February 20, 2022

First Submitted That Met QC Criteria

March 8, 2022

First Posted (Actual)

March 9, 2022

Study Record Updates

Last Update Posted (Actual)

March 9, 2022

Last Update Submitted That Met QC Criteria

March 8, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • Riphah/RCRS/REC/00940

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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