ACTIVE_NOT_RECRUITING

Comparing Perioperative Education Modalities for ACL Reconstruction on Patient Satisfaction, Self-Efficacy, and Surgical Outcomes

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 purpose of this research is to find out whether the way information about surgery is presented to patients affects patient satisfaction, knowledge retention, and surgical outcomes such as anxiety

Official Title

Comparison of Perioperative Education Modalities for ACL Reconstruction on Patient Satisfaction, Self-Efficacy, and Surgical Outcomes: A Randomized Controlled Trial

Quick Facts

Study Start:2022-08-23
Study Completion:2026-03-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT05273463

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:15 Years to 65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients of Senior Attending orthopedic sports medicine surgeons at Mayo Clinic Arizona
  2. * Patients with a proficiency in English in order to participate without need for translator.
  3. * Patients with a diagnosis of a primary ACL injury in need of surgical reconstruction utilizing any surgical technique for ACL reconstruction.
  1. * Patients with a diagnosis of ACL injury in need of a surgical revision.
  2. * Patients who have any multi-ligamentous injuries to the knee requiring modified postoperative unloading.
  3. * Patients who have history of previous anterior cruciate ligament reconstructions in either leg.
  4. * Patients who have either auditory or visual impairments.
  5. * Patients who are medical professionals with work-related knowledge of ACL reconstruction.
  6. * Patients with an inability or unwillingness of individual or legal guardian to give written informed consent.

Contacts and Locations

Principal Investigator

Hayley Powell, MSN, RN
PRINCIPAL_INVESTIGATOR
Mayo Clinic

Study Locations (Sites)

Mayo Clinic Arizona
Phoenix, Arizona, 85054
United States

Collaborators and Investigators

Sponsor: Mayo Clinic

  • Hayley Powell, MSN, RN, PRINCIPAL_INVESTIGATOR, Mayo Clinic

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 Date2022-08-23
Study Completion Date2026-03-01

Study Record Updates

Study Start Date2022-08-23
Study Completion Date2026-03-01

Terms related to this study

Keywords Provided by Researchers

  • ACL Reconstruction

Additional Relevant MeSH Terms

  • ACL Injury
  • Anterior Cruciate Ligament Injuries