Comparing Perioperative Education Modalities for ACL Reconstruction on Patient Satisfaction, Self-Efficacy, and Surgical Outcomes
NCT ID: NCT05273463
Last Updated: 2025-12-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
105 participants
INTERVENTIONAL
2022-08-23
2026-03-01
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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Video-Based Education Group
Approximately 4 weeks before scheduled surgery, participants will receive the video-based intervention regarding pre-and postoperative care for ACL reconstruction.
Video-Based Intervention
15-minute video about what to expect before, during, and after your surgery
Virtual Classroom Course Group
Approximately 4 weeks before scheduled surgery, participants will receive the classroom-based intervention regarding pre-and postoperative care for ACL reconstruction.
Classroom-Based Intervention
Virtual 30-minute course with an Orthopedic nurse about what to expect before, during, and after your surgery
Standard of Care Group
Participants will receive verbal and written pre-and postoperative instruction as typically received by all ACL reconstruction patients treated by the attending physicians before and after surgery.
No interventions assigned to this group
Interventions
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Video-Based Intervention
15-minute video about what to expect before, during, and after your surgery
Classroom-Based Intervention
Virtual 30-minute course with an Orthopedic nurse about what to expect before, during, and after your surgery
Eligibility Criteria
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Inclusion Criteria
* Patients with a proficiency in English in order to participate without need for translator.
* Patients with a diagnosis of a primary ACL injury in need of surgical reconstruction utilizing any surgical technique for ACL reconstruction.
Exclusion Criteria
* Patients who have any multi-ligamentous injuries to the knee requiring modified postoperative unloading.
* Patients who have history of previous anterior cruciate ligament reconstructions in either leg.
* Patients who have either auditory or visual impairments.
* Patients who are medical professionals with work-related knowledge of ACL reconstruction.
* Patients with an inability or unwillingness of individual or legal guardian to give written informed consent.
15 Years
65 Years
ALL
No
Sponsors
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Mayo Clinic
OTHER
Responsible Party
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Hayley R. Powell
Principal Investigator
Principal Investigators
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Hayley Powell, MSN, RN
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
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Mayo Clinic Arizona
Phoenix, Arizona, United States
Countries
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Related Links
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Mayo Clinic Clinical Trials
Other Identifiers
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21-002443
Identifier Type: -
Identifier Source: org_study_id