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Unplanned Pregnancy clinical trials

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NCT ID: NCT06324929 Recruiting - Sexual Behavior Clinical Trials

Optimizing a Digital AEP Risk Intervention With Native Women and Communities Aim 1

CARRII Native
Start date: May 16, 2024
Phase: N/A
Study type: Interventional

The purpose of this aim of the study is to gather quantitative and qualitative information to inform the development of a digital app tailored for Native American women to help them avoid a pregnancy affected by alcohol.

NCT ID: NCT06223165 Recruiting - Clinical trials for Sexually Transmitted Infections

Optimizing the Floreciendo Sexual and Reproductive Health Workshop for Latina Teens and Female Caregivers: A Pilot

Floreciendo
Start date: March 9, 2024
Phase: N/A
Study type: Interventional

Floreciendo is a sexual and reproductive health workshop for Latina teens (ages 14-18 years) and their female caregivers (e.g., mothers, sisters, grandmothers). This study involves conducting a pilot optimization trial of Floreciendo using the multiphase optimization strategy (MOST) framework. The feasibility of using a 2 x 2 x 2 factorial trial design and the acceptability and preliminary effectiveness of the intervention components of Floreciendo will be examined. This work will be conducted in partnership with community-based organizations in the Chicagoland area.

NCT ID: NCT01881321 Completed - Unplanned Pregnancy Clinical Trials

Use of Motivational Interviewing to Increase Contraception Use Among Young Women

MI RCT
Start date: June 2013
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT00997932 Completed - Unplanned Pregnancy Clinical Trials

A Pilot Study of Early Postpartum Intrauterine Contraception

ImmPPIUD
Start date: June 2009
Phase: Phase 4
Study type: Interventional

This is a prospective clinical trial of ultrasound guided intrauterine contraception insertion 10 minutes - 48 hours after vaginal delivery of single infant. A six month follow-up will entail three follow-up visits; 4-6 weeks, 3 months, and 6 months. The objective of this study is to measure intrauterine device (IUD) expulsion and the feasibility of conducting a future clinical trial to evaluate placement of the levonorgestrel-releasing intrauterine contraceptive 10 minutes - 48 hours postpartum.

NCT ID: NCT00306007 Completed - Unplanned Pregnancy Clinical Trials

Evaluation of the Reliability, Validity, and Acceptability of the London Measure of Unplanned Pregnancy in a U.S. Population of Women

LMUP
Start date: November 2005
Phase: Phase 4
Study type: Observational

The aim of the study is to evaluate the reliability, validity, and acceptability of the London Measure of Unplanned Pregnancy (LMUP) in a U.S. population of women. The researchers hypothesize that the LMUP will be acceptable to a U.S. population and will be reliable and valid.