Comparing hybrid tele-rehabilitation and in-person rehabilitation for knee osteoarthritis
The Effect of Hybrid Tele-rehabilitation Versus Standard Rehabilitation in Patients With Knee Osteoarthritis: A Single-blind Randomized Controlled Trial
This study is testing if a mix of in-person and video rehab sessions can help people with knee osteoarthritis feel better and move easier, compared to just going to in-person sessions.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 40 Years to 80 Years |
| Sex | All |
| Sponsor | King Abdulaziz University Academic / other |
| Locations | 1 site (Jeddah) |
| Trial ID | NCT06956222 on ClinicalTrials.gov |
What this trial studies
This study investigates the effectiveness of a hybrid rehabilitation approach that combines in-person and video sessions for patients with knee osteoarthritis. Participants will either attend one in-person session and one video session per week or two in-person sessions per week over an 8-week period. The study aims to assess improvements in pain, physical function, adherence to the exercise program, and participant satisfaction with the video sessions. The goal is to determine if the hybrid approach can provide similar or better outcomes compared to traditional in-person rehabilitation.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 40 to 80 with mild to moderate knee osteoarthritis and a BMI under 34.
Not a fit: Patients with severe knee osteoarthritis, those awaiting surgery, or individuals with unstable medical conditions may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could enhance accessibility to rehabilitation for patients with knee osteoarthritis, potentially improving their pain management and physical function.
How similar studies have performed: Other studies have shown promising results with tele-rehabilitation approaches, suggesting potential success for this hybrid model.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Mild to moderate knee osteoarthritis. * Age 40 to 80 years old. * Body Mass Index \< 34 kg/m2. * Numeric pain rating scale \> 4 out of 10. * Pain for more than 3 months. * Morning stiffness lasting \< 30 minutes (standard clinical criteria of knee osteoarthritis) * Pain and crepitus with active motion (e.g., walking, sit to stand, stair climbing) (standard clinical criteria of knee osteoarthritis) * Access to the device with an internet connection. * Ability to use electronic devices or smart phones. Exclusion Criteria: * Severe knee osteoarthritis and limited mobility or bonded to a wheelchair. * Body Mass Index \> 34 kg/m2 * On a waiting list for hip or knee surgery. * Undergoing other forms of rehabilitation. * Previous knee arthroplasty. * Recent knee surgery within 6 months. * Received cortisone injection within the previous 30 days. * Rheumatoid arthritis, bilateral knee morning stiffness \> 30 minutes. * Unstable medical conditions.
Where this trial is running
Jeddah
- Department of Physical Therapy, Faculty of Medical Rehabilitation Sciences, King Abdulaziz University — Jeddah, Saudi Arabia (Recruiting)
Study contacts
- Principal investigator: Anfal Astek — Department of Physical Therapy, Faculty of Medical Rehabilitation Sciences, King Abdulaziz University, Jeddah, Saudi Arabia
- Study coordinator: Anfal Astek
- Email: aastek@kau.edu.sa
- Phone: +966555668075
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.