Resisted Exercise and Kinesiology-Taping in Managing Knee Osteoarthritis
The Role of Resisted Exercise and Kinesiology-Taping in Managing Knee Osteoarthritis in Overweight and Obese Individuals.
1 other identifier
interventional
40
0 countries
N/A
Brief Summary
The study aims the Role of Resisted Exercise and Kinesiology Taping in Managing Knee Osteoarthritis in Overweight and Obese Individuals.
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 Jul 2025
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
First Submitted
Initial submission to the registry
July 3, 2025
CompletedFirst Posted
Study publicly available on registry
July 14, 2025
CompletedStudy Start
First participant enrolled
July 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 13, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 13, 2026
CompletedJuly 14, 2025
July 1, 2025
10 months
July 3, 2025
July 11, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Visual Analogue Scale (VAS)
A 10 cm horizontal line with "No Pain" (0) on the left and "Worst Pain" (10) on the right.
3 weeks
Study Arms (2)
Group A
EXPERIMENTALResisted exercises
Group B
PLACEBO COMPARATORkinesio-tapping
Interventions
Patients in this group will be applied Kinesio taping 3 times per week over the study period of 6 weeks. Before the kinesio taping, the skin surface will be clean. Patients will positioned lying on their side, hip extended, and knee joint at 60° of flexion. The knee will be tape with an I-shaped kinesio tape starting at the origin of the rectus femoris, and a Y-shaped kinesio tape proximal to the superior patellar border. The taping will be no tension at its base, whereas the portion between the anchor and the superior patella will be stretched ≈40%.
Eligibility Criteria
You may qualify if:
- Participants must have a clinical diagnosis of knee osteoarthritis, confirmed by imaging (e.g., X-ray, MRI) or a physician's diagnosis based on clinical evaluation. This ensures that participants actually have the condition being studied.
- Pain Level: Moderate pain (e.g., 3-6 on the Visual Analog Scale or VAS): Participants should experience moderate pain levels during activities of daily living (ADLs), such as walking, climbing stairs, or squatting. This level of pain should be sufficient to demonstrate the potential effects of the interventions (resisted exercise and kinesiotaping).
- Impairments related to knee pain, such as difficulty walking, bending, or climbing stairs
- Stable Medical Condition: Participants should have stable health with no significant comorbidities (e.g., uncontrolled cardiovascular diseases, severe arthritis in other joints, or neurological disorders)
You may not qualify if:
- Severe Knee Deformities or Structural Damage: Individuals with severe joint deformities or advanced OA (e.g., bone-on-bone contact as observed on radiographs) may be excluded, as they may not respond to conservative interventions like resisted exercise or kinesiotaping
- Recent Knee Surgery: Exclude participants who have undergone knee surgery (e.g., total knee replacement, arthroscopy) within the past 6-12 months, as recovery from surgery may confound the results of the study.
- Other Inflammatory Joint Disorders: Participants with other inflammatory joint diseases (e.g., rheumatoid arthritis, gout, or psoriatic arthritis) should be excluded to ensure that the results are specifically related to knee OA, not other conditions that affect the joints.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ataur Rahman, MS-PT (CPPT)
Riphah International University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 3, 2025
First Posted
July 14, 2025
Study Start
July 17, 2025
Primary Completion
May 13, 2026
Study Completion
May 13, 2026
Last Updated
July 14, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share