Anterior Cruciate Ligament Recovery With Virtual Psychological Intervention
Eligible age
13+ yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
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About this study
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.
Sponsor: Henry Ford Health System
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's recruiting
Detroit
Source: ClinicalTrials.gov · NCT05965310 · last updated 2024-12-05