Study Stopped
The project's subsidies have expired and there is a temporary lack of funding.
Telerehabilitation for Hip and Knee Osteoarthritis
1 other identifier
interventional
110
1 country
1
Brief Summary
Digital health utilization in the form of telerehabilitation is a popular technology that is very little researched for musculoskeletal disorders particularly hip and knee osteoarthritis (OA). The progression of OA will lead to total hip or knee replacement surgery. As a consequence, the advancing aging population leads to an increased burden on the healthcare system due to rising osteoarthritis. That's why, we will conduct a randomized controlled trial to explore the effectiveness of telerehabilitation in hip and knee osteoarthritis. This study will recruit OA patients into control and experimental groups. The control group will receive a patient education while the experimental group will undergo remote exercise sessions. Both groups will receive one supervised session a week for 5 weeks. The pre- and post-outcome measures will be recorded for functional status of hip and knee, muscle strength, and range of motions of the lower extremity. This innovative study will evaluate the effectiveness of a telemedicine intervention applied to a clinical population in Taiwan. The use of telerehabilitation interventions aims to reduce treatment and transportation costs, as well as save time for patients with OA. This digital health approach also helps to alleviate the workload of physiotherapists and rehabilitation doctors in clinics. The findings from this study could broaden the scope for using remote digital technology to assist clinical patients in diverse settings, especially those with limited or no hospital access.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2025
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
First Submitted
Initial submission to the registry
March 23, 2025
CompletedFirst Posted
Study publicly available on registry
March 30, 2025
CompletedStudy Start
First participant enrolled
August 6, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 26, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2026
ExpectedMay 5, 2026
April 1, 2026
5 months
March 23, 2025
April 29, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
A questionnaire
The outcome measures will be recorded before and after finish all 5 week of the intervention
Secondary Outcomes (2)
Muscle strength
The outcome measures will be recorded before and after finish all 5 week of the intervention
Range of motion
The outcome measures will be recorded before and after finish all 5 week of the intervention
Other Outcomes (2)
Borg rate of perceived exertion (RPE)
Evaluate every week for 5 weeks during each exercise session of the experimental group
International Physical Activity Questionnaire-Short Form (IPAQ-SF)
The outcome measures will be recorded before and after finish all 5 week of the intervention
Study Arms (2)
Telerehabilitation
EXPERIMENTALReceive a remote exercise program for 40 minutes once a week for 5 weeks
Standard care
PLACEBO COMPARATORReceive a patient education session once a week for 5 weeks
Interventions
Exercise program include Warm-up, Targeted muscle Strengthening, Joint mobilization, and Proprioception
Education session on their pain, disability, and functional activities
Eligibility Criteria
You may qualify if:
- diagnosed with hip or knee osteoarthritis within last one year
- having sub-acute or chronic symptoms of pain and functional disability
- living in an area served by high-speed Internet services (at least 512 kb/s in upload)
- living within an hour driving distance from the treating hospital
- physically fit to provide a written consent to participate in this study
You may not qualify if:
- taking sedatives, autoimmune, or other medication that can interfere with their exercise program
- any health issues that could affect the tests or the rehabilitation program, including surgery over the recent six months
- having diagnosed with cognitive disorders
- having recent surgery or major postoperative complications
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Taipei Medical University-Shuang Ho Hospital, Ministry of Health and Welfare
New Taipei City, 235, Taiwan
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Hung-Chou Chen, Dr.
Taipei Medical University Shuang Ho Hospital
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 23, 2025
First Posted
March 30, 2025
Study Start
August 6, 2025
Primary Completion
December 26, 2025
Study Completion (Estimated)
December 1, 2026
Last Updated
May 5, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share