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Application of Smart Wearable Device-Based Telerehabilitation in Postoperative Recovery Following Arthroscopic Surgery for Discoid Meniscus: A Prospective, Randomized Controlled Trial Protocol

Application of Smart Wearable Device-Based Telerehabilitation in Postoperative Recovery Following Arthroscopic Surgery for Discoid Meniscus: A Prospective, Randomized Controlled Trial Protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122921
Enrollment
Unknown
Registered
2026-04-20
Start date
2026-04-30
Completion date
Unknown
Last updated
2026-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Discoid meniscus

Interventions

Clinic rehabilitation group:Postoperatively, patients received systematic on-site rehabilitation guidance from a therapist and were permitted to continue rehabilitation at home independently only afte
Telerehabilitation group:Postoperatively, patients underwent systematic telerehabilitation training assisted by smart wearable devices.

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 10 and 60 years. 2.Diagnosed with a discoid meniscus injury, confirmed by both magnetic resonance imaging (MRI) and arthroscopy. 3.Underwent arthroscopic partial meniscectomy (saucerization) with concomitant suture repair. 4.Willing to participate in the clinical trial and comply with the follow-up protocol.

Exclusion criteria

Exclusion criteria: 1.Presence of concomitant injuries in the same knee, such as ligament tears, fractures, or cartilage lesions. 2.Kellgren & Lawrence osteoarthritis grade greater than II. 3.History of trauma or surgery in other weight-bearing joints of the lower limb (e.g., ankle ligament tears, osteonecrosis of the femoral head) that could indirectly affect knee joint loading and movement.

Design outcomes

Primary

MeasureTime frame
Knee pain score VAS score;Tegner score for knee function assessment;IKDC score of knee function assessment;Lysholm score for knee function assessment;Ikeuchi;3D gait analysis;Knee range of motion;Limb Circumference;Muscle Strength;Return to Sport Assessment;

Secondary

MeasureTime frame
MRI T2 Mapping;Patient Satisfaction;Rehabilitation Adherence;X-ray;Minimal Clinically Important Difference (MCID);Patient accepted symptom status(PASS);Significant clinical benefit(SCB);

Countries

China

Contacts

Public ContactJian Li

West China Hospital, Sichuan University

18980601388@163.com+86 189 8060 1388

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026