Brief, Behavioral Intervention to Reduce Douching Among Adolescent and Young Women
This study has suspended participant recruitment.
Sponsor:
Collaborator:
Tulane University School of Public Health and Tropical Medicine
Information provided by:
Centers for Disease Control and Prevention
ClinicalTrials.gov Identifier:
NCT00207480
First received: September 13, 2005
Last updated: NA
Last verified: September 2005
History: No changes posted
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Purpose
This study will implement and test a brief, tailored individual-level intervention to be used in two New Orleans adolescent clinics with female patients aged 16-24 who douche.
| Condition | Intervention | Phase |
|---|---|---|
|
Vaginal Douching Bacterial Vaginosis |
Behavioral: Brief, motivational interviewing intervention |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Educational/Counseling/Training |
| Official Title: | Brief, Behavioral Intervention to Reduce Douching Among Adolescent and Young Women |
Further study details as provided by Centers for Disease Control and Prevention:
| Estimated Enrollment: | 270 |
| Study Start Date: | October 2004 |
The study implements a client-centered behavioral intervention (CCBI) based on Prochaska’s Transtheoretical Model of Change (TMC) and the intervention will use Miller’s Motivational Interviewing (MI) techniques. This intervention will be evaluated using (1) an audio/computer-assisted self-administered interview (ACASI) survey to assess changes in respondents’ douching knowledge, attitudes, and practices, and (2) biological testing for Bacterial Vaginosis.
Eligibility| Ages Eligible for Study: | 16 Years to 24 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Women attending between the ages of 16 and 24 who have douched at least once in the last 180 days, agree to a test for Bacterial Vaginosis, and agree to allow us to contact you by telephone or in person for a follow-up interview and testing for bacterial vaginosis.
Exclusion Criteria:
- currently pregnant, non-English speaking
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00207480
Locations
| United States, Louisiana | |
| Orleans Women's Health Clinic | |
| New Orleans, Louisiana, United States, 70119 | |
Sponsors and Collaborators
Tulane University School of Public Health and Tropical Medicine
Investigators
| Principal Investigator: | Patricia Kissinger, PhD, RN | Tulane University School of Public Health and Tropical Medicine |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00207480 History of Changes |
| Other Study ID Numbers: | CDC-NCHSTP-4415, U36/CCU300430-24 |
| Study First Received: | September 13, 2005 |
| Last Updated: | September 13, 2005 |
| Health Authority: | United States: Federal Government |
Additional relevant MeSH terms:
|
Vaginosis, Bacterial Bacterial Infections Vaginitis Vaginal Diseases Genital Diseases, Female |
ClinicalTrials.gov processed this record on May 19, 2013