Mobile app to help recovery after hip, knee, or spine surgery
Official title: Using a Mobile Application for In-Bed Conditioning Exercises for Orthopedic Postoperative Patients
Run by Yale University · NCT06407427 · Data updated 2026-11-12
We will test a mobile app that prompts in-bed conditioning exercises to help people over 65 recover after hip fracture fixation, spinal fusion, or total hip/knee replacement.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Yale University Academic / other |
| Locations | 1 site (New Haven, Connecticut) |
| Status | Recruiting |
| Started | July 21, 2025 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | August 5, 2026 |
| Trial ID | NCT06407427 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are patients aged over 65 who are recovering from low-energy hip fracture fixation, total hip or knee arthroplasty, or single-to-multilevel spinal fusion, who are alert, can follow two-step commands, and own a mobile phone.
✕Probably not a fit
Patients with severe cognitive impairment, neurologic paralysis, major polytrauma restricting anti-gravity exercises, knee immobilization, or unstable medical conditions requiring ventilatory or high oxygen support are unlikely to benefit or qualify.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a prospective, single-arm pilot enrolling older adults recovering from hip fracture fixation, spinal fusion, or total hip/knee arthroplasty at Yale New Haven Hospital Saint Raphael's Campus. Participants who are cognitively able and own a mobile phone will use an app that sets reminders and adjusts in-bed exercise difficulty based on patient feedback. The study will track app usage, patient satisfaction, and physical therapy outcomes and will collect therapist feedback. Initial enrollment is 15 patients with a planned expansion to a randomized controlled trial of 50 participants per arm if pilot results support it.
Why it matters
Potential benefit: If successful, the app could improve early mobility, adherence to prescribed exercises, and short-term rehabilitation outcomes after orthopedic surgery.
How similar studies have gone: Prior studies of mobile apps for postoperative or home-based physical therapy have shown modest gains in exercise adherence and function, but high-quality evidence in older postoperative orthopedic populations remains limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
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 exercises * Knee immobilization, bed rest * Unstable medical conditions: * On ventilatory support * Utilizing high degrees of oxygen support (continuous BiPAP, high flow nasal cannula, nonrebreather mask, aerosol mask \>3L/min) * Hemodynamic instability requiring pressor medication support (can include those on pressors for elevated mean arterial pressure goals (MAPs)) * Neurologically instable with strokes, hemorrhages, increased intracranial pressures * Open wounds or surgical incisions * Tenuous closed wounds requiring immobilization or bending restrictions * Open wounds that are either packed/dressed or dressed with a wound vacuum * Surgical wounds that are draining fluid or purulence * Vulnerable populations * Incarcerated individuals * Patients without access to a mobile phone with iOS capability
Where it's running
-
Yale New Haven Hospital Saint Raphael's Campus
New Haven, Connecticut, United States Recruiting
Study contacts
- Principal investigator: Rajiv S Vasudevan, M.D. — Yale University
- Study coordinator: Rajiv S Vasudevan, M.D.
- Email: Rajiv.vasudevan@yale.edu
- Phone: 650-714-7908
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Evaluating a new surgical irrigation method for joint replacement surgeries
This study is testing a new way to clean the surgical area during knee or hip replacement surgeries to see if it can lower the risk of infections compared to the usual method.
-
Comparing Remimazolam and Propofol for Delirium After Surgery
This study is testing whether remimazolam or propofol is better at preventing confusion after surgery in older patients getting hip or knee replacements.
-
Collecting data on Taperloc Complete stems for hip surgeries
This study is trying to see how safe and effective the Taperloc Complete hip implants are for people who have had hip surgery, by looking at both past patients and following new ones over the years.
-
Effects of virtual reality on walking in adults with knee osteoarthritis
This study tests how immersive virtual reality environments—designed to feel safe or to provoke fear—affect walking and worry about movement in adults 50 and older with knee osteoarthritis and in healthy peers.
-
Weekly berobenatide for knee osteoarthritis in adults who are overweight or obese
This study tests whether weekly berobenatide helps reduce knee pain and improve function, while also affecting body weight, in adults with knee osteoarthritis who are overweight or obese (with or without type 2 diabetes).
-
Autologous adipose-derived stem cell injections for knee osteoarthritis
We’re testing whether injecting a patient’s own fat-derived stem cells into the knee can help people with knee OA feel less pain and move better, compared with a standard hyaluronic acid treatment.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.