Evaluating the Efficacy of a Video Based Intervention to Educate Teen Moms About Fetal Alcohol Syndrome (FAS)

Sponsor
Texas Tech University Health Sciences Center (Other)
Overall Status
Terminated
CT.gov ID
NCT00747630
Collaborator
(none)
99
1
1
44.1
2.2

Study Details

Study Description

Brief Summary

Evaluating the efficacy of a video about FAS to determine whether it has an impact on knowledge about FAS and their likelihood to participate in risk taking behavior.

Condition or Disease Intervention/Treatment Phase
  • Other: An educational video about Fetal Alcohol Syndrome
Early Phase 1

Detailed Description

Teenage mothers are asked to participate in the study and then randomized into an intervention or control group. Both groups take a multiple choice survey and then are randomized to either watch a video about FAS or not. After the video (or not for the controls) they then take a post video short answer survey. The survey results are then scored and statistical analysis performed to determine whether the video intervention increased their knowledge about FAS and their likelihood to drink alcohol during pregnancy.

Study Design

Study Type:
Interventional
Actual Enrollment :
99 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Evaluating the Efficacy of a Video Based Intervention to Educate Teen Moms About Fetal Alcohol Syndrome
Study Start Date :
May 1, 2006
Actual Primary Completion Date :
Jan 1, 2010
Actual Study Completion Date :
Jan 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

The group selected to watch the video.

Other: An educational video about Fetal Alcohol Syndrome
A 20 minute video about FAS

Outcome Measures

Primary Outcome Measures

  1. To determine whether an educational video on FAS increases maternal knowledge on the subject and affects their likelihood to drink alcohol. [Immediate]

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 16 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Pregnant teens aged 12 to 16 years
Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Grand Expectations Lubbock Texas United States 79430

Sponsors and Collaborators

  • Texas Tech University Health Sciences Center

Investigators

  • Principal Investigator: Tammy Camp, MD, Texas Tech Department of Pediatrics

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Texas Tech University Health Sciences Center
ClinicalTrials.gov Identifier:
NCT00747630
Other Study ID Numbers:
  • FAS Study
First Posted:
Sep 5, 2008
Last Update Posted:
Dec 17, 2012
Last Verified:
Dec 1, 2012
Keywords provided by Texas Tech University Health Sciences Center
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 17, 2012