Ignite Creation Date:
2024-05-06 @ 8:26 PM
Last Modification Date:
2024-10-26 @ 3:28 PM
Study NCT ID:
NCT06386549
Status:
RECRUITING
Last Update Posted:
2024-04-26
First Post:
2024-03-25
Brief Title:
Effect of a Tele-rehabilitation Programme in Children With Burns a Randomized Controlled Trial
Sponsor:
LIAO Peng
Organization:
The Hong Kong Polytechnic University
Study Overview
Official Title:
Effect of a Tele-rehabilitation Programme in Children With Burns a Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-04
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 goal of this clinical trial is to compare tele-rehabilitation and routine post-discharge rehabilitation in children with burn injuries The main questions it aims to answer are
Is tele-rehabilitation better for improving the quality and outcomes of care for burn children
Is tele-rehabilitation more effective in improving scar management in children with burns injuries
Is tele-rehabilitation more effective in improving perceived stress in parents of children with burns injuries
Is tele-rehabilitation better for improving the quality and outcomes of care for burn children
Is tele-rehabilitation more effective in improving scar management in children with burns injuries
Is tele-rehabilitation more effective in improving perceived stress in parents of children with burns injuries
Detailed Description:
In this study experimental group received a 12-week tele-rehabilitation program which included face-to-face access to silicone pads pressure garments splint and other tools necessary for burn recovery The tele-rehabilitation program was used for intervention and regular follow-up
The control group also received a 12-week follow-up but only on the basis of face-to-face access to silicone pads pressure garments splint and other tools necessary for burn recovery
Researchers will compare whether the trial group has better the quality and outcomes of care and scarring for children and parents who perceived stress
The control group also received a 12-week follow-up but only on the basis of face-to-face access to silicone pads pressure garments splint and other tools necessary for burn recovery
Researchers will compare whether the trial group has better the quality and outcomes of care and scarring for children and parents who perceived stress
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