Ignite Creation Date:
2024-05-06 @ 7:51 PM
Last Modification Date:
2024-10-26 @ 3:15 PM
Study NCT ID:
NCT06162052
Status:
RECRUITING
Last Update Posted:
2024-02-21
First Post:
2023-11-29
Brief Title:
Impact of a Telerehabilitation Program With Technology Enhancement on Post-burn Recovery
Sponsor:
The University of Texas Medical Branch Galveston
Organization:
The University of Texas Medical Branch Galveston
Study Overview
Official Title:
Impact of a Telerehabilitation Program With Technology Enhancement on Post-burn Recovery
Status:
RECRUITING
Status Verified Date:
2024-02
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:
The purpose of this study is to examine the effect of participating in a tele-rehabilitation program after a burn
Detailed Description:
This is a prospective single center randomized trial comparing a traditional approach to physical therapy to a technology-enhanced approach following a burn We hypothesize that with the implementation of a novel telerehabilitation program incorporating technology enhancement range of motion and quality of life can be improved To test the hypothesis in future grant applications this pilot study will be used to determine feasibility collect preliminary data vet endpoints and gain patient feedback To achieve these necessary goals we will compare two methods of supporting home performance of prescribed physical and occupational therapy Standard S patients will be equipped with paper instructions for their physical therapy exercises and Technology-Enhanced TE support patients will be given paper instructions set up with a habit and productivity application Avocation that gamifies tasks and tracks achievements a Fitbit activity tracker a logbook and have virtual movement therapy once weekly with an exercise physiologist for a total of four weeks
Specific Aim 1 To determine whether range of motion is altered with TE Range of motion in the affected joints will be measured by goniometry self-reported by patient and measured by study staff in the clinic
Specific Aim 2 To determine whether TE with prescribed movement affects scar pain and quality of life
Specific Aim 1 To determine whether range of motion is altered with TE Range of motion in the affected joints will be measured by goniometry self-reported by patient and measured by study staff in the clinic
Specific Aim 2 To determine whether TE with prescribed movement affects scar pain and quality of life
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