Evaluating the Impact of Video Discharge Instructions for Mohs Surgery Post-Operative Care

Sponsor
Case Comprehensive Cancer Center (Other)
Overall Status
Terminated
CT.gov ID
NCT02970435
Collaborator
(none)
14
1
2
23.3
0.6

Study Details

Study Description

Brief Summary

The purpose of this research is to look at how educational videos provided by doctors might affect patients knowledge, satisfaction, confidence, and anxiety with post-operative Mohs surgery care. Patients will be randomized to either: 1) a group that receives educational videos in addition to standard-of-care written and verbal instructions or 2) a group that receives only standard-of-care written and verbal instructions.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Video Discharge Instructions
  • Behavioral: Telecommunication Reminders
  • Behavioral: Standard of Care
N/A

Detailed Description

The Primary Objective of this study is to determine if video discharge instructions, when added to standard of care written and verbal instructions, lead to a decrease in unnecessary phone calls from patients in a Mohs dermatology clinic.

The Secondary Objectives of this study are to determine if video discharge instructions, when added to standard of care written and verbal instructions, help to improve patients' satisfaction with education materials provided by the clinic, improve patients' knowledge of post-operative management, improve patients' confidence in taking care of their suture site post-operatively, and reduce post-operative anxiety about their suture site.

This study will be a randomized controlled trial in which the impact of video discharge instructions on patient calls, anxiety, and confidence will be evaluated. Patients will be randomized using a permuted block model generated through SAS.

Study Design

Study Type:
Interventional
Actual Enrollment :
14 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Evaluating the Impact of Video Discharge Instructions for Mohs Surgery Post-Operative Care
Actual Study Start Date :
Jul 12, 2017
Actual Primary Completion Date :
May 1, 2018
Actual Study Completion Date :
Jun 21, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Video Discharge Instructions

These videos contain the same instructions that a patient receives via the standard-of-care verbal and written discharge instructions. These instructions will be delivered by the same nursing and medical staff that also regularly provides verbal and written discharge instructions to patients. There will be no difference in the content between the standard-of-care verbal and written instructions and the video discharge instructions. Patients in this group will receive telecommunication reminders on how to access discharge videos.

Behavioral: Video Discharge Instructions
The video discharge instructions, will be provided to the patient at the time of surgical procedure.

Behavioral: Telecommunication Reminders
Telecommunication reminders including text messages, email, or phone calls to remind participants how to access the video discharge instruction up to three times before follow-up

Behavioral: Standard of Care
Standard of Care: verbal and written discharge instructions for patients after surgery

Active Comparator: Verbal and Written Discharge Instructions

Nursing and medical staff will provide verbal and written discharge instructions as is standard of care post surgery

Behavioral: Standard of Care
Standard of Care: verbal and written discharge instructions for patients after surgery

Outcome Measures

Primary Outcome Measures

  1. Ratio of patients in the intervention group who call the clinic compared to percentage of patients in the control group who call the clinic [Up to 8 weeks after discharge]

    Researchers will record when each participant calls the clinic. The number of people who call in the intervention group will be compared to the number of people who call in the control group. This will give an efficacy measure of the video discharge instructions

Secondary Outcome Measures

  1. Difference in knowledge of discharge instructions in intervention group versus control group [Up to 8 weeks after discharge]

    Answers to survey questions investigating knowledge of discharge instruction will be compared between the control and intervention groups.

  2. Difference in confidence in intervention group versus control group [Up to 8 weeks after discharge]

    A survey investigating confidence about Mohs surgery post-operative care will be used in this study. This survey will be quantified using the Likert scale.

  3. Difference in satisfaction in intervention group versus control group [Up to 8 weeks after discharge]

    A survey investigating patient satisfaction about Mohs surgery post-operative care will be used in this study. This survey will be quantified using the Likert scale.

  4. Difference in self reported anxiety levels in intervention group versus control group [Up to 8 weeks after discharge]

    A survey investigating anxiety about Mohs surgery post-operative care will be used in this study. This survey will be quantified using the Likert scale.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients who underwent a linear closure on the face at UH Mohs clinic

  • Fluent English speakers

Exclusion Criteria:

● Non-fluent English speakers

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospitals at Cleveland Medical Center, Seidman Cancer Center, Case Comprehensive Cancer Center Cleveland Ohio United States 44106-5065

Sponsors and Collaborators

  • Case Comprehensive Cancer Center

Investigators

  • Principal Investigator: Jeremy Bordeaux, MD, University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Case Comprehensive Cancer Center
ClinicalTrials.gov Identifier:
NCT02970435
Other Study ID Numbers:
  • CASE1616
First Posted:
Nov 22, 2016
Last Update Posted:
Jan 25, 2021
Last Verified:
Jan 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Case Comprehensive Cancer Center

Study Results

No Results Posted as of Jan 25, 2021