Anterior Cruciate Ligament Recovery With Virtual Psychological Intervention
Recruiting now · Not applicable
Conditions studied: Depression, Anterior Cruciate Ligament Injuries, Mental Health Issue
In brief
The goal of this parallel arm prospective randomized control trial study is to compare outcomes in Anterior Cruciate Ligament Reconstruction (ACLR) Surgery patients after exposure to a virtual psychological intervention (VPI) versus standard care. The main question the investigators are asking is if virtual administration of psychological CBT modules will be an accessible and convenient vehicle to improve ACLR outcomes. Participants will be placed either into a treatment group receiving virtual modules of cognitive behavioral therapy in addition to standard of care ACLR surgery or the control group receiving only the standard of care ACLR surgery. The investigators hypothesize that ACLR patients in the VPI cohort will have improved return to sport and post operative outcomes compared to controls.
Key facts
- Study ID
- NCT05965310
- Run by
- Henry Ford Health System
- People needed
- 60
- Starts
- 2023-09-01
- Expected to finish
- 2025-12-31
- Last updated by the study team
- 2024-12-05
Who can join
Age: 13 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients over the age of 12 with ACL injuries undergoing ACLR with a Henry Ford Sports Orthopedic Surgeon
- First time ACLR on the injured knee
You may not qualify if…
- Patients undergoing revision ACL surgery
- Concomitant posterior cruciate ligament injury of the involved knee
- Systemic or local infection pre-operatively
- Systemic administration of any type of corticosteroid or immunosuppressive agents within 30 days of surgery
- History of rheumatoid arthritis, inflammatory arthritis, or autoimmune diseases
- Pregnancy
Where it is running
- Henry Ford Health System — Detroit, Michigan, United States (enrolling)
Full record on ClinicalTrials.gov
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