Ignite Creation Date:
2024-05-11 @ 8:31 AM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06407427
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-05-31
First Post:
2024-05-06
Brief Title:
Evaluating the Efficacy of a Mobile Application in Postoperative Rehabilitation
Sponsor:
Yale University
Organization:
Yale University
Study Overview
Official Title:
Using a Mobile Application for In-Bed Conditioning Exercises for Orthopedic Postoperative Patients
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study aims to evaluate the effectiveness of a mobile application in improving postoperative rehabilitation outcomes among patients undergoing orthopedic surgery
Detailed Description:
The study aims to assess the effectiveness of a mobile app-based tool in improving conditioning mobility and physical therapy performance among patients recovering from orthopedic surgery particularly hip fracture fixation spinal fusion and total kneehip arthroplasty The app sets reminders for in-bed conditioning exercises with difficulty levels adjusted based on patient feedback The prospective single-arm pilot study will enroll patients over 65 years old with adequate cognitive status and a mobile phone Patient performance on the app satisfaction metrics and physical therapy outcomes will be evaluated along with feedback from physical therapists The study is conducted through the Yale New Haven Health System with plans to enroll 15 patients initially and subsequently expand to a randomized controlled trial with 50 participants in each arm The goal is to improve outcomes in this population characterized by poor mobility morbidity and mortality rates by supplementing inpatient rehabilitation with targeted app-prompted exercises
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None