RECRUITING

Anterior Cruciate Ligament Recovery With Virtual Psychological Intervention

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2023-09-01
Study Completion:2025-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05965310

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:13 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients over the age of 12 with ACL injuries undergoing ACLR with a Henry Ford Sports Orthopedic Surgeon
  2. * First time ACLR on the injured knee
  1. * Patients undergoing revision ACL surgery
  2. * Concomitant posterior cruciate ligament injury of the involved knee
  3. * Systemic or local infection pre-operatively
  4. * Systemic administration of any type of corticosteroid or immunosuppressive agents within 30 days of surgery
  5. * History of rheumatoid arthritis, inflammatory arthritis, or autoimmune diseases
  6. * Pregnancy

Contacts and Locations

Study Contact

Brittaney Pratt
CONTACT
8502842125
bpratt1@hfhs.org

Principal Investigator

Thomas Sean Lynch, MD
PRINCIPAL_INVESTIGATOR
Henry Ford Health System

Study Locations (Sites)

Henry Ford Health System
Detroit, Michigan, 48202
United States

Collaborators and Investigators

Sponsor: Henry Ford Health System

  • Thomas Sean Lynch, MD, PRINCIPAL_INVESTIGATOR, Henry Ford Health System

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-09-01
Study Completion Date2025-12-31

Study Record Updates

Study Start Date2023-09-01
Study Completion Date2025-12-31

Terms related to this study

Additional Relevant MeSH Terms

  • Depression
  • Anterior Cruciate Ligament Injuries
  • Mental Health Issue