Evaluating the Efficacy of a Mobile Application in Postoperative Rehabilitation
This study aims to evaluate the effectiveness of a mobile application in improving postoperative rehabilitation outcomes among patients undergoing orthopedic surgery.
| Condition(s) | Spine Degeneration, Hip Arthritis, Knee Osteoarthritis, Hip Fractures |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | This study aims to evaluate the effectiveness of a mobile application in improving postoperative rehabilitation outcomes among patients undergoing orthopedic surgery. |
| Who can participate | Inclusion Criteria: * Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * English reading/speaking * Are status post low-energy hip fracture, total knee/hip arthroplasty, or single to multilevel spinal fusion without paralysis * Must be able bodied enough to participate in a mobile app tool for physical therapy * Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration\] Exclusion Criteria: * Severe cognitive impairment: Not alert and oriented to person, place, time, and reason for being the hospital; and unable to follow 2 step commands * Severe physical impairment: * Neurologic paralysis * Polytraumas with restrictions incompatible with anti-gravity |
| Ages | 18 Years |
| Sex | All |
| Lead sponsor | Yale University |
| Locations | New Haven, Connecticut, United States |
| Start date | 2025-07-21 |
| NCT ID | NCT06407427 |
| Official listing | https://clinicaltrials.gov/study/NCT06407427 |