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Anterior Cruciate Ligament Recovery With Virtual Psychological Intervention

Recruiting

Randomized Control Trial of the Impact of a Virtual Psychological Intervention on the Outcomes of ACLR

Who can join

Ages 13 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* 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

Exclusion Criteria:

* 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

About the 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.

What is being tested

Sponsor: Henry Ford Health System · Participants: 60 · Started: Sep 1, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT05965310

Locations in the U.S.

MichiganHenry Ford Health System, Detroit

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.