RecruitingNot ApplicableNCT05965310

Anterior Cruciate Ligament Recovery With Virtual Psychological Intervention

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


Sponsor

Henry Ford Health System

Enrollment

60 participants

Start Date

Sep 1, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 13 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a virtual psychological support program can help young people recover better — both physically and mentally — after ACL reconstruction surgery (a procedure to repair a torn knee ligament). **You may be eligible if...** - You are over 12 years old - You tore your ACL and are having ACL reconstruction surgery for the first time on that knee - Your surgery is being performed by a Henry Ford Sports Orthopedic surgeon **You may NOT be eligible if...** - You are having revision (repeat) ACL surgery on that knee - You also have a posterior cruciate ligament (PCL) injury in the same knee - You have an active infection before surgery - You are on corticosteroids or immunosuppressants within 30 days of surgery - You have rheumatoid arthritis, inflammatory joint disease, or other conditions affecting the knee's recovery Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALVirtual Psychological Intervention: Cognitive Behavioral Therapy

An asynchronous course of pre- and post-operative CBT modules (VPI) will be delivered to patients in Group A as an adjuvant treatment to standard-of-care rehabilitation.


Locations(1)

Henry Ford Health System

Detroit, Michigan, United States

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NCT05965310


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