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NCT00552539 Clinical Trial

Syphilis Video Tool to Promote Knowledge and Testing in the ED

Syphilis Clinical Trial

Official title:
Video Tool to Promote Syphilis Knowledge and Testing in the Emergency Department

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00552539
Other study ID # 06431
Secondary ID
Status Completed
Phase N/A
First received October 31, 2007
Last updated October 31, 2007
Start date June 2006
Est. completion date August 2006

Study information
Verified date October 2007
Source Jacobi Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The objective of this study is to determine whether the "Syphilis and Men" educational video can be a useful tool to increase syphilis knowledge and testing among English and Spanish-speaking urgent care and emergency department patients, regardless of various self-reported characteristics that increase their risk for syphilis infection.

Description:

A randomized four-group intervention-control Solomon design was implemented with Group 1 participants receiving a pre-test survey, the educational video intervention, and a post-test survey; Group 2 the pre-test and post-test surveys; Group 3 the video intervention and a post-test survey; and Group 4 the post-test survey. This design was selected to assess the effect of the video in increasing syphilis knowledge while controlling for the influence of the pre-test instrument in potentially sensitizing participants to key facts. A computer-generated randomization list was created and used to assign patients to groups.

Recruitment information / eligibility
Status Completed
Enrollment 220
Est. completion date August 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- Patients aged 18-55 years of age were eligible only if they spoke English or Spanish.

Exclusion Criteria:

- Patients were excluded if clinically unstable, unarousable, hearing impaired or visually impaired despite corrected lens.

Study Design

Allocation: Randomized, Intervention Model: Factorial Assignment, Masking: Single Blind (Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Other:
• 'educational video'
'educational video'

Locations
Country Name City State
United States Jacobi Medical Center Bronx New York

Sponsors (2)
Lead Sponsor Collaborator
Jacobi Medical Center Public Health Solutions

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary The primary outcome was the score on a 10-question measure designed to assess knowledge attained from the educational video. 20 minutes
Secondary A secondary outcome was the decision to be tested for syphilis. 20 minutes
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