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NCT03344497 Clinical Trial

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

Dermatology/Skin - Other Clinical Trial

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

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03344497
Other study ID # 1702192435
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2017
Est. completion date February 1, 2018

Study information
Verified date November 2017
Source University of Arizona
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 45
Est. completion date February 1, 2018
Est. primary completion date February 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Male and female, at least 18 years of age

2. Subjects scheduled to undergo outpatient skin surgery

3. Subjects able to comprehend and read the English language.

Exclusion Criteria:

1. Subjects unable to or unwilling to comply with the study procedures

2. Subjects unable to speak or read the English language.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• VC Group
VC (Conventional Consultation/Video) Group

Locations
Country Name City State
United States University of Arizona - Banner University Medicine Dermatology Tucson Arizona

Sponsors (1)
Lead Sponsor Collaborator
University of Arizona

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pre-operative anxiety levels assessed via questionnaire Preoperative anxiety and information scale will be collected. 1 day
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