Virtual reality program for preoperative rehabilitation in ACL surgery patients
The Application of a Preoperative Rehabilitation Program Based on Virtual Reality (VR) Technology in Patients Undergoing Anterior Cruciate Ligament (ACL) Reconstruction
This study is testing whether a virtual reality program can help patients get ready for ACL surgery by improving their exercises, support, and education compared to standard care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 120 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | First Affiliated Hospital of Shantou University Medical College Academic / other |
| Locations | 1 site (Shantou, Guangdong) |
| Trial ID | NCT06347523 on ClinicalTrials.gov |
What this trial studies
This clinical trial involves 120 patients scheduled for anterior cruciate ligament (ACL) reconstruction surgery at the First Affiliated Hospital of Shantou University Medical College. Participants will be randomly assigned to either a control group receiving standard nursing care or an experimental group that will engage in a virtual reality (VR)-based preoperative rehabilitation program. The VR program includes personalized exercise prescriptions and educational content aimed at improving psychological support and nutritional guidance. The study will assess various outcomes, including knee joint range of motion, function scores, and patient satisfaction, comparing results between the two groups.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18 to 60 who are undergoing their first ACL reconstruction and have adequate communication skills.
Not a fit: Patients with cognitive impairments, severe sensory deficits, or limb paralysis may not benefit from this study.
Why it matters
Potential benefit: If successful, this program could enhance recovery outcomes and patient satisfaction for those undergoing ACL reconstruction.
How similar studies have performed: Other studies have shown promise in using VR technology for rehabilitation, suggesting potential success for this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Individuals eligible for inclusion in the study are those who undergo their initial anterior cruciate ligament (ACL) reconstruction surgery, aged between 18 and 60 years, possess adequate hearing and vision, have clear consciousness, and demonstrate proficient language communication skills. Exclusion Criteria: * Individuals with cognitive impairments, severe hearing or vision impairments, limb paralysis, or non-compliance with the experiment will be excluded from participation.
Where this trial is running
Shantou, Guangdong
- "The First Affiliated Hospital of Shantou University Medical College — Shantou, Guangdong, China (Recruiting)
Study contacts
- Study coordinator: Xiaolian Li, Master
- Email: Lxl0754@163.com
- Phone: 13822800990
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.