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

Sponsor
Mayo Clinic (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05273463
Collaborator
(none)
105
1
3
4
26.2

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Video-Based Intervention
  • Behavioral: Classroom-Based Intervention
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
105 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Comparison of Perioperative Education Modalities for ACL Reconstruction on Patient Satisfaction, Self-Efficacy, and Surgical Outcomes: A Randomized Controlled Trial
Anticipated Study Start Date :
Aug 1, 2022
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: 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.

Behavioral: Video-Based Intervention
15-minute video about what to expect before, during, and after your surgery

Experimental: 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.

Behavioral: Classroom-Based Intervention
Virtual 30-minute course with an Orthopedic nurse about what to expect before, during, and after your surgery

No Intervention: 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.

Outcome Measures

Primary Outcome Measures

  1. Patient Satisfaction [24 months]

    Measured using the Leiden Perioperative Patient Satisfaction Questionnaire. Self-reported questionnaire that rates the subjects satisfaction with information provision, discomfort and needs during perioperative care.

Secondary Outcome Measures

  1. Anxiety [24 months]

    Measured using the PROMIS Emotional Distress - Anxiety Short Form 8a. Self-reported 8-item questionnaire that rates the subjects emotional distress in the past 7 days on a scale of 1=Never to 5=Always. Higher total scores indicate higher anxiety severity.

  2. Self-Efficacy [24 months]

    Measured using the PROMIS Self-Efficacy - Manage Symptoms Short Form 8a. Self-reported 8-item questionnaire that rates the subjects current level of confidence to statements about managing symptoms using a scale of 1="I am not at all confident to 5="I am very confident". Higher total score indicate higher confidence in managing symptoms.

  3. Kinesiophobia [24 months]

    Measured using the Tampa Scale for Kinesiophobia. Self-reported 17-item questionnaire based on evaluation of fear of movement, fear of physical activity, and fear avoidance using a scale of 1=Strongly Disagree to 4=Strongly Agree. Total score range from 17-68 and higher scores indicate severe kinesiophobia.

  4. Physical Function [24 months]

    Measured using the PROMIS Physical Function Short Form 10b. Self-reported 10-item questionnaire that rates the subjects ability to perform an activity using a scale of 5="Without any difficulty" to 1="Unable to do". Higher total scores indicate higher physical function.

  5. Knowledge Retention [24 months]

    Measured using the ACL Reconstruction Perioperative Education Quiz

  6. Pain Interference [24 months]

    Measured using the PROMIS Pain Interference Short Form 6a. Self-reported 6-item questionnaire that rates the subjects pain interference with activities in the past 7 days using a scale of 1="Not at all" to 5="Very much". Higher total scores indicate higher pain interference with activities experienced.

  7. History of Falls [24 months]

    Measured using the History of Falls Questionnaire. Self-reported 5-item questionnaire asking subjects about falls experienced in the past month and seriousness.

  8. Lysholm Knee Score [24 months]

    Measured using the Lysholm Knee Scoring Scale. Self-reported questionnaire that asks subjects to indicate which statement best describes their condition in regards to common complaints frequently experience with knee problems. Total scoring out of 100 and higher score less knee-specific symptoms.

  9. Activity Level [24 months]

    Measured using the Tegner Activity Scale. Self-reported level of activity prior to injury and post injury. Total of 10 levels and higher levels indicate greater activity level.

  10. Confidence in Returning to Sport [24 months]

    Measured using the ACL Return to Sport Index. Self-reported 6-item questionnaire to measure the readiness to return to sports after ACL injury or reconstruction. Using a scale from 0 points (extremely negative psychological responses) to 100 points (no negative psychological responses).

  11. Resilience [24 months]

    Measured using the Brief Resilience Scale. Self-reported 6-item questionnaire to measure perceived ability to recover from stress. Total score range 1-5 with higher scores indicating higher resilience.

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic Arizona Phoenix Arizona United States 85054

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Hayley Powell, RN, BSN, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Hayley R. Powell, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT05273463
Other Study ID Numbers:
  • 21-002443
First Posted:
Mar 10, 2022
Last Update Posted:
Aug 10, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hayley R. Powell, Principal Investigator, Mayo Clinic
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 10, 2022