Home-based rehabilitation program for knee recovery after ligament surgery
Effectiveness of the KC@H Programme Compared With Clinic-based Rehabilitation in Patients Recovering From Anterior Cruciate Ligament Reconstruction: Study Protocol for a Single-centre, Randomised Controlled Superiority Trial.
NA · University of Évora · NCT05828355
This study tests whether a home-based rehab program with online exercises can help people recover better after knee ligament surgery compared to traditional clinic visits.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 56 (estimated) |
| Ages | 18 Years to 55 Years |
| Sex | All |
| Sponsor | University of Évora (other) |
| Locations | 1 site (Évora) |
| Trial ID | NCT05828355 on ClinicalTrials.gov |
What this trial studies
This program aims to evaluate the effectiveness of a home-based rehabilitation approach for patients recovering from anterior cruciate ligament reconstruction compared to traditional clinic-based rehabilitation. It includes internet-based therapeutic exercises that patients can perform at home, potentially improving access to rehabilitation services. The study will measure patient-reported outcomes, clinician-reported outcomes, and physical performance metrics to assess the program's impact on recovery. A randomized controlled trial design will be employed to ensure robust results.
Who should consider this trial
Good fit: Ideal candidates are adults who have undergone primary anterior cruciate ligament reconstruction and have a healthy opposite knee.
Not a fit: Patients with significant lower limb injuries, mental health disorders requiring medication, or severe communication or balance impairments may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could enhance recovery outcomes for patients undergoing knee ligament surgery by providing more accessible rehabilitation options.
How similar studies have performed: Other studies have shown promise in using home-based rehabilitation approaches for similar conditions, indicating potential for success in this novel application.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Undergone primary ACLR regardless of surgical method and choice of autograft. * Have a healthy contralateral (opposite) knee. * The time between ACL injury and ACLR should not exceed 12 months. Exclusion Criteria: * Declined to participate. * Concomitant osteochondral injuries. * Undergone multiple reconstructions of the lateral collateral ligament or posterior cruciate ligament. * Significant lower limb injuries within the 12 months before the ACL injury. * Medical conditions that may affect recovery. * Using medication for mental health disorders. * Severe impairments in communication or balance.
Where this trial is running
Évora
- Hospital da Misericórdia de Évora — Évora, Portugal (RECRUITING)
Study contacts
- Principal investigator: João Paulo Sousa, PhD — Universidade de Évora - Comprehensive Health Research Center
- Study coordinator: João Paulo Sousa, PhD
- Email: jsousa@uevora.pt
- Phone: 919662332
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.
Conditions: Anterior Cruciate Ligament Reconstruction, Patient-reported Outcomes Measures, Clinician-reported Outcomes Measures, Functional Performance, Clinical Relevance, Internet-based Intervention, Exercise Therapy