Effects of Hip Abductors Strengthening In Knee Osteoarthritis
Comparison of Hip Abductors and Quadriceps Strengthening With Quadriceps Strengthening Alone in Knee Osteoarthritis
1 other identifier
interventional
40
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2021
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
January 30, 2022
CompletedFirst Submitted
Initial submission to the registry
February 20, 2022
CompletedFirst Posted
Study publicly available on registry
March 9, 2022
CompletedMarch 9, 2022
March 1, 2022
14 days
February 20, 2022
March 8, 2022
Conditions
Outcome Measures
Primary Outcomes (2)
Numeric Pain Rating Scale (NPRS)
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)
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 Outcomes (1)
Five Times Sit to Stand Test (FTSST)
6 weeks
Study Arms (2)
Hip Abductor Strengthening
EXPERIMENTALThis group received quadriceps and hip abductor strengthening along with patellar mobilization and stretching exercises.
Traditional Physical Therapy
ACTIVE COMPARATORThis group received quadriceps strengthening along with patellar mobilization and stretching exercises.
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- Osteoarthritis of single or both knees
- Kellgren Lawrence scale between 2-4
You may not qualify if:
- Knee valgus or varus deformity
- Hip or knee joint replacement
- Tibial osteotomy
- Any other surgery of hip or knee joint
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Khattak Physiotherapy and Rehabilitation Center
Mansehra, Khyber Pakhtunkhwa, 21300, Pakistan
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad Affan Iqbal, PhD*
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Study is single blinded Randomized control Trials.patients are randomly allocated into two groups through lottery method.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 20, 2022
First Posted
March 9, 2022
Study Start
January 1, 2021
Primary Completion
January 15, 2021
Study Completion
January 30, 2022
Last Updated
March 9, 2022
Record last verified: 2022-03
Data Sharing
- IPD Sharing
- Will not share