Effect of 0° and 50° N-K Table Load Angles on Quadriceps Activation in Knee Osteoarthritis
Comparative Effectiveness of N-K Table Load Angles at 0° and 50° on Quadriceps Femoris Maximum Voluntary Contraction in Patients With Knee Osteoarthritis
1 other identifier
interventional
43
1 country
1
Brief Summary
Knee osteoarthritis (OA) is a common degenerative joint disease that leads to pain, reduced mobility, and functional limitation. Quadriceps femoris weakness plays a significant role in disease progression and disability. Isotonic strengthening using the N-K Table allows adjustment of load angles to optimize muscle activation; however, the effect of different load angles on quadriceps activation in patients with knee osteoarthritis remains unclear. This study aims to compare quadriceps femoris activation at 0° and 50° N-K Table load angles in patients with knee osteoarthritis using surface electromyography (sEMG). A randomized cross-over experimental design is applied to determine whether adjusting the load angle improves maximum voluntary contraction (MVC) during isotonic knee extension exercise.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable knee-osteoarthritis
Started Jan 2024
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 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 5, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
May 25, 2025
CompletedFirst Submitted
Initial submission to the registry
February 25, 2026
CompletedFirst Posted
Study publicly available on registry
March 6, 2026
CompletedMarch 6, 2026
March 1, 2026
5 months
February 25, 2026
March 4, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Maximum Voluntary Contraction (MVC) of Quadriceps Femoris Muscles
Maximum voluntary contraction (MVC) of the quadriceps femoris muscles (vastus medialis, rectus femoris, and vastus lateralis) measured using surface electromyography (sEMG) during isotonic knee extension exercise performed on the N-K Table at 0° and 50° load angles. MVC is defined as the highest sEMG amplitude recorded from three maximal voluntary contraction trials for each muscle.
Day 1
Study Arms (2)
0° Load Angle NK Table
EXPERIMENTALParticipants performed isotonic knee extension exercise using the N-K Table adjusted to a 0° load angle. Exercise intensity was set at 75% of the individual 10-repetition maximum (10RM). Each participant performed controlled knee extension movements from 90° flexion to near full extension. At each load angle, three maximal voluntary contractions were recorded with 3-second rest intervals between trials. Surface electromyography (sEMG) was used to measure maximum voluntary contraction (MVC) of the vastus medialis, vastus lateralis, and rectus femoris muscles.
50° Load Angle NK Table
EXPERIMENTALParticipants performed isotonic knee extension exercise using the N-K Table adjusted to a 50° load angle. Exercise intensity was set at 75% of the individual 10-repetition maximum (10RM). Each participant performed controlled knee extension movements from 90° flexion to near full extension. At each load angle, three maximal voluntary contractions were recorded with 3-second rest intervals between trials. Surface electromyography (sEMG) was used to measure maximum voluntary contraction (MVC) of the vastus medialis, vastus lateralis, and rectus femoris muscles.
Interventions
Isotonic knee extension exercise performed using the N-K Table device at specified load angles (0° and 50°) with resistance set at 75% of 10RM.
Eligibility Criteria
You may qualify if:
- Diagnosed with unilateral or bilateral knee osteoarthritis (OA), grade 2 or 3, in the subacute or chronic phase based on the criteria of the American College of Rheumatology (ACR) and Kellgren-Lawrence classification.
- Female, aged 50-65 years, based on ACR diagnostic criteria.
- Knee flexion-extension range of motion of at least 0-120 degrees.
- Normal cognitive function as assessed using the Montreal Cognitive Assessment Indonesia Version (MoCA-INA) (score ≥26-30)
You may not qualify if:
- Knee joint instability due to ligament laxity in the cruciate or collateral ligaments obtained from physical examination (valgus/varus test and anterior/posterior drawer test) or previous supporting examination.
- Presence of deformity in the form of genu varus, genu valgus, or genu recurvatum (Q angle 12-20°).
- History of knee injury (fracture, ligament rupture, or meniscus) or having undergone knee surgery.
- Pain or instability of the ankle joint obtained from physical examination.
- Stroke or disorders of the central and peripheral nervous system.
- Patients with metabolic diseases such as diabetes mellitus and heart disease or other autoimmune diseases based on medical records in unstable condition with pre-prandial capillary blood glucose ≠ 80-130 mg/dL or 1-2 hours post-prandial capillary blood glucose ≠ \<180 mg/dL, systolic blood pressure ≠ 90-140 mmHg and diastolic blood pressure ≠ 60-90 mmHg.
- Pain durin loaded knee extension exercise greatetr than 3 on the Visual Analogue Scale (VAS)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department of Physical Medicine and Rehabilitation, Dr. Cipto Mangunkusumo General Hospital
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 is an open-label study. Due to the nature of the exercise intervention, participants and investigators are aware of the load angle applied during testing.
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- researcher
Study Record Dates
First Submitted
February 25, 2026
First Posted
March 6, 2026
Study Start
January 20, 2024
Primary Completion
June 5, 2024
Study Completion
May 25, 2025
Last Updated
March 6, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share
There is no plan to share individual participant data.