Skip to main content
Clinical Trials/NCT03344497
NCT03344497CompletedNot Applicable

Animated Video Consultation for Reducing Pre-Operative Anxiety in Outpatient Dermatologic Surgery

University of Arizona1 site in 1 country45 target enrollmentStarted: June 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
45
Locations
1
Primary Endpoint
Pre-operative anxiety levels assessed via questionnaire

Study Overview

Brief Summary

The purpose of this study is to evaluate whether the addition of an animated skin surgery educational video to conventional in-person surgery consultation will help reduce pre-operative anxiety in patients awaiting outpatient skin surgery.

Detailed Description

This will be an randomized controlled pilot study. Subjects will be randomized to either receive an animated video along with conventional consultation OR receive a conventional consultation only. Pre-operative anxiety will be assessed.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Male and female, at least 18 years of age
  • •Subjects scheduled to undergo outpatient skin surgery
  • •Subjects able to comprehend and read the English language.

Exclusion Criteria

  • •Subjects unable to or unwilling to comply with the study procedures
  • •Subjects unable to speak or read the English language.

Arms & Interventions

VC (Conventional Consultation/Video) Group

Other

Subjects will receive conventional consultation and watch an animated video.

Intervention: VC Group (Other)

CC (Conventional Consultation) Group

No Intervention

Subjects will receive conventional consultation only. Subjects will cross-over to receive animated video at the end.

Outcomes

Primary Outcomes

Pre-operative anxiety levels assessed via questionnaire

Time Frame: 1 day

Preoperative anxiety and information scale will be collected.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials