Eccentric Versus Concentric Quadriceps Exercises in Knee Osteoarthritis
Differences in Improvements of Knee Range of Motion, Muscle Strength, and Functional Capacity Between Eccentric and Concentric Quadriceps Femoris Exercises in Patients With Knee Osteoarthritis
1 other identifier
interventional
24
1 country
1
Brief Summary
This study aims to compare the effectiveness of eccentric and concentric quadriceps femoris strengthening exercises in patients with knee osteoarthritis. Knee osteoarthritis is a common musculoskeletal condition that causes pain, reduced joint movement, muscle weakness, and functional limitations. Participants will be assigned to perform either eccentric or concentric unilateral open kinetic chain quadriceps exercises using isotonic loading based on a 10-repetition maximum (10-RM). The exercise program will be conducted three times per week for six weeks. The primary objective is to evaluate differences in quadriceps muscle strength between the two exercise approaches. Secondary outcomes include changes in knee range of motion and functional capacity measured using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC). The results of this study are expected to provide evidence to guide exercise prescription in rehabilitation programs for patients with knee osteoarthritis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable knee-osteoarthritis
Started Jul 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 13, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 21, 2025
CompletedFirst Submitted
Initial submission to the registry
March 4, 2026
CompletedFirst Posted
Study publicly available on registry
March 10, 2026
CompletedMarch 11, 2026
March 1, 2026
11 months
March 4, 2026
March 9, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Quadriceps Muscle Strength
Quadriceps muscle strength measured in kilograms using the 10-repetition maximum (10-RM) method on the NK Table. The outcome is defined as the difference between baseline and post-intervention values at six weeks.
Baseline and Week 6
Study Arms (2)
Eccentric Exercise Group
EXPERIMENTALParticipants perform unilateral open kinetic chain full-arc quadriceps strengthening exercises emphasizing eccentric contraction using isotonic loading based on a 10-repetition maximum (10-RM), three times weekly for six weeks.
Concentric Exercise Group
EXPERIMENTALParticipants perform unilateral open kinetic chain full-arc quadriceps strengthening exercises emphasizing concentric contraction using isotonic loading based on a 10-repetition maximum (10-RM), three times weekly for six weeks.
Interventions
Unilateral isotonic quadriceps strengthening emphasizing eccentric contraction using the NK Table, 3 sessions per week for 6 weeks, intensity based on 10-RM. Weeks 1-3: 3 sets of 6 repetitions; Weeks 4-6: 3 sets of 8 repetitions.
Unilateral isotonic quadriceps strengthening emphasizing concentric contraction using the NK Table, 3 sessions per week for 6 weeks, intensity based on 10-RM. Weeks 1-3: 3 sets of 6 repetitions; Weeks 4-6: 3 sets of 8 repetitions.
Eligibility Criteria
You may qualify if:
- Female participants aged 40-59 years
- Diagnosed with unilateral or bilateral knee osteoarthritis based on American College of Rheumatology (ACR) criteria and Kellgren-Lawrence grade II-III
- Knee pain lasting more than 3 months with Numeric Rating Scale (NRS) score 1-3
- Limited knee flexion range of motion
You may not qualify if:
- History of unstable cardiovascular, respiratory, or metabolic disease
- Knee joint instability due to cruciate or collateral ligament laxity or meniscal injury
- Previous knee surgery
- History of knee intra-articular injection within the last 3 months
- Cognitive impairment (Montreal Cognitive Assessment Indonesian Version \[MoCA-Ina\] score \< 26)
- Clinical signs of tendinopathy characterized by pain during active knee extension (open or closed kinetic chain)
- Balance disorders
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Physical Medicine and Rehabilitation
Jakarta, DKI Jakarta, 10430, Indonesia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This study is conducted as an open-label trial. Participants and treating therapists are aware of the assigned exercise intervention (eccentric or concentric quadriceps strengthening). No blinding of participants, care providers, or outcome assessors is performed.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- researcher
Study Record Dates
First Submitted
March 4, 2026
First Posted
March 10, 2026
Study Start
July 15, 2024
Primary Completion
June 13, 2025
Study Completion
November 21, 2025
Last Updated
March 11, 2026
Record last verified: 2026-03