Syphilis Video Tool to Promote Knowledge and Testing in the ED
Primary Purpose
Syphilis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
'educational video'
Sponsored by
About this trial
This is an interventional prevention trial for Syphilis focused on measuring syphilis, educational video, knowledge, black, Hispanic
Eligibility Criteria
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.
Sites / Locations
- Jacobi Medical Center
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
No Intervention
Experimental
No Intervention
Arm Label
1
2
3
4
Arm Description
pre test survey, educational video, post test survey
no intervention
educational video and post test survey
post test survey
Outcomes
Primary Outcome Measures
The primary outcome was the score on a 10-question measure designed to assess knowledge attained from the educational video.
Secondary Outcome Measures
A secondary outcome was the decision to be tested for syphilis.
Full Information
NCT ID
NCT00552539
First Posted
October 31, 2007
Last Updated
October 31, 2007
Sponsor
Jacobi Medical Center
Collaborators
Public Health Solutions
1. Study Identification
Unique Protocol Identification Number
NCT00552539
Brief Title
Syphilis Video Tool to Promote Knowledge and Testing in the ED
Official Title
Video Tool to Promote Syphilis Knowledge and Testing in the Emergency Department
Study Type
Interventional
2. Study Status
Record Verification Date
October 2007
Overall Recruitment Status
Completed
Study Start Date
June 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2006 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Jacobi Medical Center
Collaborators
Public Health Solutions
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief 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.
Detailed 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Syphilis
Keywords
syphilis, educational video, knowledge, black, Hispanic
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
220 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
pre test survey, educational video, post test survey
Arm Title
2
Arm Type
No Intervention
Arm Description
no intervention
Arm Title
3
Arm Type
Experimental
Arm Description
educational video and post test survey
Arm Title
4
Arm Type
No Intervention
Arm Description
post test survey
Intervention Type
Other
Intervention Name(s)
'educational video'
Intervention Description
'educational video'
Primary Outcome Measure Information:
Title
The primary outcome was the score on a 10-question measure designed to assess knowledge attained from the educational video.
Time Frame
20 minutes
Secondary Outcome Measure Information:
Title
A secondary outcome was the decision to be tested for syphilis.
Time Frame
20 minutes
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yvette Calderon, MD, MS
Organizational Affiliation
Jacobi Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
John P Sanchez, MD, MPH
Organizational Affiliation
Jacobi Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Jacobi Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Syphilis Video Tool to Promote Knowledge and Testing in the ED
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