Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06407427

Evaluating the Efficacy of a Mobile Application in Postoperative Rehabilitation

Led by Yale University · Updated on 2025-09-02

100

Participants Needed

1

Research Sites

49 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to evaluate the effectiveness of a mobile application in improving postoperative rehabilitation outcomes among patients undergoing orthopedic surgery.

CONDITIONS

Official 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...

  • Provision of signed and dated informed consent form
  • Willingness to comply with all study procedures and be available for the study duration
  • Able 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-based physical therapy
  • Agreement to adhere to lifestyle considerations throughout the study duration
Not Eligible

You will not qualify if you...

  • Severe cognitive impairment preventing alertness, 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 neurologic instability
  • Presence of open wounds or surgical incisions requiring immobilization or with drainage
  • Vulnerable populations including 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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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.

CONTACT

D

David Gargano, PA-C

CONTACT

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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