Improving Contraceptive Counseling in the United States
Completed · Not applicable
Conditions studied: New Behavioral Protocol, Treatment as Usual
In brief
This project develops a contraceptive counseling protocol (CCP) grounded in scientific evidence and evaluates the CCP for promoting behaviors conducive to preventing unintended pregnancy among women. The project develops and refines the CCP using focus groups and in-depth interviews with (a) key administrators in the national office of Planned Parenthood (b) key administrators in participating Title X clinics, (c) contraceptive counselors, and (d) clients of the health centers. The CCP uses scientifically grounded principles for guiding effective decision making and provider-client communication. Ten Title X clinics are randomly assigned to one of two conditions (5 clinics per condition): (1) treatment as usual (TAU) or (2) implementation of the CCP. Approximately 150 women are selected for study participation in each clinic, yielding about 1,400 participants (half control and half CCP). Immediately following their counseling session, women complete a computer-administered interview that serves as a fidelity check and permits evaluation of the effects of the CCP on variables associated with counseling satisfaction. All women are re-interviewed by phone 6 months later and 12 months later. The effect of the CCP on method-choice effectiveness, method switching, gaps in protection, and use accuracy are evaluated.
Key facts
- Study ID
- NCT02801266
- Run by
- New York University
- People needed
- 1418
- Starts
- 2012-10-01
- Expected to finish
- 2015-10-01
- Last updated by the study team
- 2022-11-02
Who can join
Age: 18 and older, up to 30. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Must be seeking contraception from clinic on day of recruitment
You may not qualify if…
- Not seeking contraception from clinic on day of recruitment
Where it is running
- New York University, Silver School of Social Work — New York, New York, United States
Full record on ClinicalTrials.gov
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