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

Mayo Clinic logo

Mayo Clinic

Status

Active, not recruiting

Conditions

Anterior Cruciate Ligament Injuries
ACL Injury

Treatments

Behavioral: Classroom-Based Intervention
Behavioral: Video-Based Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT05273463
21-002443

Details and patient eligibility

About

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

Enrollment

105 estimated patients

Sex

All

Ages

15 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients of Senior Attending orthopedic sports medicine surgeons at Mayo Clinic Arizona
  • 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 with a diagnosis of ACL injury in need of a surgical revision.
  • 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.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

105 participants in 3 patient groups

Video-Based Education Group
Experimental group
Description:
Approximately 4 weeks before scheduled surgery, participants will receive the video-based intervention regarding pre-and postoperative care for ACL reconstruction.
Treatment:
Behavioral: Video-Based Intervention
Virtual Classroom Course Group
Experimental group
Description:
Approximately 4 weeks before scheduled surgery, participants will receive the classroom-based intervention regarding pre-and postoperative care for ACL reconstruction.
Treatment:
Behavioral: Classroom-Based Intervention
Standard of Care Group
No Intervention group
Description:
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.

Trial contacts and locations

1

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Central trial contact

Sailesh Tummala, MD; Kaycee Glattke, PhD

Data sourced from clinicaltrials.gov

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