Use of Motivational Interviewing to Increase Contraception Use Among Young Women (MI RCT)
|ClinicalTrials.gov Identifier: NCT01881321|
Recruitment Status : Completed
First Posted : June 19, 2013
Last Update Posted : July 30, 2014
Study design: This is a 2-phase study. During the first phase, the investigators developed a contraceptive counseling intervention based on the principles of Motivational Interviewing, trained counselors, and conducted a small pilot study to develop skills and refine the intervention.
The second phase is this feasibility randomized controlled trial (RCT) to compare outcomes between:
Group 1 - Women randomized to a 20-40 minute contraceptive counseling session based on the principles of motivational interviewing, vs.
Group 2 - Women receiving usual clinic care.
Population: Women, aged 15-29 years, presenting to the University of Chicago family planning clinic for termination of an unintended pregnancy.
Hypothesis: A larger proportion of women who are randomized to receive the MI counseling intervention will be using very effective contraception 3 months after the intervention.
|Condition or disease||Intervention/treatment|
|Unplanned Pregnancy||Behavioral: Counseling Intervention|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||60 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Official Title:||Use of Motivational Interviewing to Increase Contraception Use Among Young Women: a Randomized Control Trial|
|Study Start Date :||June 2013|
|Primary Completion Date :||March 2014|
|Study Completion Date :||March 2014|
Experimental: Group 1: Counseling Intervention
Contraceptive counseling session based on the principles of motivational interviewing
Behavioral: Counseling Intervention
20-40 minute contraceptive counseling session based on the principles of motivational interviewing
No Intervention: Group 2: Usual Care
The standard clinic-based contraceptive counseling with no additional or theory-based contraceptive counseling session
- Use of very effective contraception [ Time Frame: up to 3 months after termination of pregnancy appointment ]
- Correct, consistent use of contraceptive method [ Time Frame: up to 3 months ]
- Use of any contraceptive method [ Time Frame: up to 3 months ]
- Contraceptive method satisfaction [ Time Frame: up to 3 months ]
- Intention to continue current method [ Time Frame: up to 3 months ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01881321
|United States, Illinois|
|University of Chicago Medical Center|
|Chicago, Illinois, United States, 60615|
|Principal Investigator:||Amy Whitaker, MD MS||University of Chicago|