No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
13 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
60 (estimated)
Sponsor
Henry Ford Health System · Other
Who this trial is looking for
This trial is looking for patients who are having surgery for their first ACL injury. Participants will receive either virtual therapy along with standard care after surgery or just standard care to see which helps them recover better.
Are You a Good Fit for This Trial?
You may be able to join if
I am over 12 years old.
I have an ACL injury.
I am having my first ACL reconstruction surgery on my injured knee.
I am seeing a Henry Ford Sports Orthopedic Surgeon.
You may not be able to join if
I am having revision ACL surgery.
I have a posterior cruciate ligament injury.
I have an infection before surgery.
I have taken corticosteroids or immunosuppressants in the last 30 days.
I have a history of rheumatoid arthritis or other autoimmune diseases.
I am pregnant.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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…
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.
Trial Locations
Loading…
Loading trial locations…
Facility
City
State
Country
Status
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 kne…
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
Picking one helps us show the most relevant trials first.
Your results are loading in the background — you can
change this any time from the results page.
Set your location to continue
Find My Trials uses your location to surface clinical trials near you.
Add your city or zip code to your profile and try again.