Actively Recruiting
Using a Mobile Application for In-Bed Conditioning Exercises for Orthopedic Postoperative Patients
Led by Yale University · Updated on 2025-09-02
100
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness of a mobile application designed to improve rehabilitation outcomes in patients recovering from orthopedic surgeries such as hip fracture fixation, spinal fusion, and total knee or hip arthroplasty. This prospective, single-arm pilot study focuses on patients over 65 years old with adequate cognitive function and mobile phone access. The goal is to supplement inpatient rehabilitation with app-prompted in-bed conditioning exercises to enhance mobility and physical therapy performance in a population at risk for poor mobility and higher morbidity. Participants will be randomly assigned to receive either usual post-operative care alone or usual care plus the use of the mobile app. The app provides reminders for in-bed conditioning exercises, adjusting difficulty based on patient feedback. The initial pilot will enroll 15 patients, with plans to expand to a randomized controlled trial including 50 participants per group. Physical therapists will also provide feedback on the app's usability and patient interaction to assess feasibility. During the study, patient performance during physical therapy will be measured from postoperative day 1 to discharge (approximately days 3-5). Other assessments include patient satisfaction, length of hospital stay, pain scores, app usage, exercise compliance, and adverse events up to 90 days. Physical therapists will monitor setup assistance and app use for up to 120 days. Total participation duration varies, with assessments conducted mainly during the hospital stay and follow-up for safety and feasibility.
CONDITIONS
Brief Title
Evaluating the Efficacy of a Mobile Application in Postoperative Rehabilitation
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Signed and dated informed consent form
- Willingness to comply with all study procedures and availability for the study duration
- Ability to read and speak English
- Status post low-energy hip fracture, total knee/hip arthroplasty, or single to multilevel spinal fusion without paralysis
- Physically able to participate in mobile app-assisted physical therapy
- Agreement to follow lifestyle considerations throughout the study
You will not qualify if you...
- Severe cognitive impairment preventing orientation and following two-step commands
- Severe physical impairments including neurologic paralysis, polytraumas restricting anti-gravity exercises, knee immobilization, or bed rest
- Unstable medical conditions such as ventilatory support, high oxygen support, hemodynamic instability requiring pressors, or neurological instability
- Open wounds or surgical incisions requiring immobilization or showing drainage or infection
- Vulnerable populations such as incarcerated individuals
- Lack of access to a mobile phone with iOS capability
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 3 to 5 days during hospital stay
Participants use a mobile application to assist with in-bed conditioning exercises as part of their post-operative rehabilitation after orthopedic surgery. The app sets reminders and adjusts exercise difficulty based on participant feedback.
Daily use of the app with physical therapy visits approximately over 3 to 5 days
Duration - Up to 90 to 120 days
Participants and physical therapists provide feedback on app usability and patient performance, with monitoring for any adverse events.
Periodic assessments during follow-up period
Trial Site Locations
Total: 1 location
1
Yale New Haven Hospital Saint Raphael's Campus
New Haven, Connecticut, United States, 06510
Actively Recruiting
Research Team
R
Rajiv S Vasudevan, M.D.
D
David Gargano, PA-C
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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