- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05272124
Effects of Hip Abductors Strengthening In Knee Osteoarthritis
Comparison of Hip Abductors and Quadriceps Strengthening With Quadriceps Strengthening Alone in Knee Osteoarthritis
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Khyber Pakhtunkhwa
-
Mansehra, Khyber Pakhtunkhwa, Pakistan, 21300
- Khattak Physiotherapy and Rehabilitation Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Riphah/RCRS/REC/00940
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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