Ignite Creation Date:
2024-05-06 @ 8:20 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06347523
Status:
RECRUITING
Last Update Posted:
2024-05-14
First Post:
2024-03-22
Brief Title:
VR-Based Preoperative Rehabilitation Program for Patients Undergoing Anterior Cruciate Ligament ACL Reconstruction
Sponsor:
First Affiliated Hospital of Shantou University Medical College
Organization:
First Affiliated Hospital of Shantou University Medical College
Study Overview
Official Title:
The Application of a Preoperative Rehabilitation Program Based on Virtual Reality VR Technology in Patients Undergoing Anterior Cruciate Ligament ACL Reconstruction
Status:
RECRUITING
Status Verified Date:
2024-05
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:
Between April 2 2024 and October 1 2024 a study will be conducted at the Department of Orthopedics in the First Affiliated Hospital of Shantou University Medical College involving 120 patients who will undergo anterior cruciate ligament reconstruction surgery They will be randomly divided into two groups an experimental group and a control group
Detailed Description:
The control group will receive standard nursing care while the experimental group will receive an enhanced preoperative rehabilitation program incorporating Virtual Reality VR technology This program will include patient assessments personalized exercise prescriptions and VR-based educational videos covering psychological support nutritional guidance and exercise instructions
Patients in the experimental group will use VR headsets for preoperative and postoperative interactive training sessions as well as for viewing postoperative educational videos The intervention will start upon admission and will continue until discharge
Primary outcome measures will include knee joint range of motion and the Lysholm knee function score Secondary measures will encompass anxiety depression pain scores activities of daily living time to ambulation postoperative complications and patient satisfaction
Statistical analysis will be conducted to compare outcomes between the two groups
Patients in the experimental group will use VR headsets for preoperative and postoperative interactive training sessions as well as for viewing postoperative educational videos The intervention will start upon admission and will continue until discharge
Primary outcome measures will include knee joint range of motion and the Lysholm knee function score Secondary measures will encompass anxiety depression pain scores activities of daily living time to ambulation postoperative complications and patient satisfaction
Statistical analysis will be conducted to compare outcomes between the two groups
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