Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06407427

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

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

Post-operative Follow-up

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

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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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