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NCT01881321 · ClinicalTrials.gov registry record · NA
Use of Motivational Interviewing to Increase Contraception Use Among Young Women
A NA study of Unplanned Pregnancy, sponsored by University of Chicago.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
- 1
- Study location
NCT01881321: Completed NA study of Unplanned Pregnancy, sponsored by University of Chicago.
NCT01881321 is a NA study of Unplanned Pregnancy that has completed, run by University of Chicago. The registered enrollment target is 60 participants, below the 191-participant average among 3 other Unplanned Pregnancy trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01881321, a NA study of Unplanned Pregnancy, has completed, sponsored by University of Chicago.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Conditions Studied
Interventions
- BEHAVIORAL Counseling Intervention
Study Locations (1)
Illinois
- University of Chicago Medical Center - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2013-06 |
| Est. Completion | 2014-03 |
| Phase | NA |
What the finished NCT01881321 record still lists
NCT01881321 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 191-participant average among 3 other Unplanned Pregnancy trials with a reported enrollment target (69% lower).
The record links to 1 condition, with Unplanned Pregnancy appearing as the primary indexed condition, and to 1 intervention - of which Counseling Intervention is the first listed.
NCT01881321 reports a single indexed study location in Illinois.
Frequently Asked Questions
What is clinical trial NCT01881321 about?
NCT01881321 is a clinical study titled "Use of Motivational Interviewing to Increase Contraception Use Among Young Women". 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 ph...
What is the current status of trial NCT01881321?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2013-06. Estimated completion is 2014-03.
What conditions does trial NCT01881321 study?
This clinical trial studies the following conditions: Unplanned Pregnancy.
What interventions are being tested in trial NCT01881321?
The interventions under investigation include: Counseling Intervention (BEHAVIORAL).
Who is sponsoring clinical trial NCT01881321?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01881321 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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