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Contraception Behavior clinical trials

View clinical trials related to Contraception Behavior.

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NCT ID: NCT03486743 Completed - Clinical trials for Contraception Behavior

Assessment of Cultural Acceptability of Long Acting Contraception in a Diverse, Urban Population

Start date: April 15, 2018
Phase: N/A
Study type: Interventional

Preliminary data from our work with teen mothers suggest that many women would benefit from contraception but do not actually make visits nor initiate conversations regarding contraception unless the subject is raised by the clinician. Those coming for primary care visits discuss their conditions and care with family and friends, spreading health care information. A substantial proportion of citizens obtain their health information from friends, family, internet, social media and other non-clinicians. Thus, educating women, even when not coming expressly for contraceptive services, increases more accurate health information throughout their communities and actually identifies fertility needs, ultimately increasing use of contraception.

NCT ID: NCT03448289 Completed - Primary Health Care Clinical Trials

Use of a Reproductive Life Planning Tool at the Pediatric Well-Baby Visit With Postpartum Women

Start date: January 24, 2018
Phase: N/A
Study type: Interventional

Improved access to timely health care and contraception in the postpartum (PP) period is needed to reduce unintended pregnancies and help women achieve desired birth spacing. While the routine 6-week visit has historically been considered the place for women to discuss and receive contraception, many women, particularly low-income women, do not attend the postpartum visit. A novel approach to increasing receipt of PP care and contraception is the adoption of a reproductive life planning tool. Explorations of the use of a self-administered Reproductive Life Plan Tool (RLPT) by pediatricians in the context of the Well-Baby Visit (WBV) with postpartum mothers, holds great promise. The objective of this study is to determine whether use of a simple self-administered Reproductive Life Plan Tool at the 2-month WBV increases the proportion of postpartum women receiving woman's health care and contraception at 6-months PP, compared to women not exposed to such an intervention. The two specific aims of the project are: 1) To determine if introducing a self-administered Reproductive Life Planning Tool (RLPT) with postpartum mothers during the 2-month WBV will increase the proportion of women receiving a well-woman primary care health visit by 6 months postpartum; and if introducing a self-administered Reproductive Life Planning Tool (RLPT) will increase utilization rates of contraception by 6 months postpartum. 2) To assess patient-, provider-, and systems-level barriers and facilitators to integrating a self-administered Reproductive Life Planning Tool (RLPT) designed to facilitate referral of postpartum women for primary well-woman care in the context of a pediatric clinic. The investigators hypothesize that exposure to a self-administered RLPT combined with a conversation with a pediatrician during a 2-month WBV will increase use of well-woman primary health care during the postpartum period as well as receipt of contraception, by 6-months postpartum. If successful, the results of this study have great potential to inform clinical and public health practice to increase women's use of health care and contraception in the postpartum period.

NCT ID: NCT03404284 Completed - Contraception Clinical Trials

Assessment of Family Planning and Immunization Service Integration in Malawi

Start date: June 2016
Phase: N/A
Study type: Observational

This is a mixed methods process evaluation of a programmatic intervention to integrate family planning and immunization services at health facilities and through outreach services in Dowa and Ntchisi districts of Malawi. The study involved qualitative methods (in depth interviews and focus group discussions with service providers, mothers and fathers of infants <1 year, and supervisors and program managers) as well as secondary analysis of service statistics for family planning and immunization services and of supervision reports.

NCT ID: NCT03400449 Completed - Contraceptive Usage Clinical Trials

Video Versus Conversational Contraceptive Counseling During Maternity Hospitalization

Start date: April 28, 2015
Phase: N/A
Study type: Interventional

A randomized trial comparing LARC uptake and satisfaction after either video or conversational-based contraceptive counseling for pregnant women in labor.

NCT ID: NCT03400410 Completed - Clinical trials for Contraception Behavior

Hormonal Contraceptive Health Education for Adolescent Males

Start date: May 21, 2018
Phase: N/A
Study type: Interventional

Prospective randomized control trial of an educational electronic application on female hormonal contraception for adolescent males in the pediatric emergency department.

NCT ID: NCT03366636 Completed - Clinical trials for Sexually Transmitted Diseases

Project Legacy Impact Evaluation Study

Start date: October 30, 2017
Phase: N/A
Study type: Interventional

This study will design and rigorously evaluate the efficacy of Project Legacy, a five week positive youth development intervention to decrease sexual risk for unintended pregnancies and STIs among youth experiencing homelessness or at risk of homelessness aged 14-19. This randomized control trial will compare Project Legacy to a usual services control.

NCT ID: NCT03224390 Completed - Clinical trials for Contraception Behavior

A Pilot Study to Estimate the Impact of a Screening and Referral Service on Contraceptive Use

Start date: July 12, 2017
Phase: N/A
Study type: Interventional

The specific aim of this pilot study is to estimate the impact of a new digital health service on the uptake of family planning among Kenyan women with an unmet need for contraception. Enrolled women will be randomized to a control arm or an encouragement arm that will receive a special invitation to try the new service.

NCT ID: NCT03165838 Completed - Pregnancy Related Clinical Trials

Effectiveness of Shortened Time Interval to Postpartum Visit in Improving Postpartum Attendance

Start date: November 18, 2013
Phase: N/A
Study type: Interventional

Due to potential to improve family planning, clinicians are increasingly interested in shortening the time to postpartum visits, but lack an evidence base to change policy.There are no studies that have examined the effectiveness of shortened interval to postpartum visit on attendance rate, contraception use, and rapid repeat of pregnancy (RROP). With this research, the investigators propose to conduct a randomized controlled trial (RCT) to examine the effect of reduced time interval to postpartum visit (3-4 weeks rather than 6-8 weeks) on postpartum visit attendance rate, contraceptive use, and RROP.

NCT ID: NCT03106805 Withdrawn - Clinical trials for Contraception Behavior

Early Versus Late Interval Postpartum Copper Intrauterine Device Insertion

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

The optimal interval between pregnancies is debated, but a duration greater than 11-18 months has been suggested as reducing complications in the subsequent pregnancy. Improved birth spacing can be a key benefit use of long-acting reversible contraception, but delay to initiation can still be problematic.So women who have recently given birth can be cost-effectively targeted for family planning education and engagement because often they are already connected with health professionals

NCT ID: NCT03012659 Active, not recruiting - Contraceptive Usage Clinical Trials

Contraceptive Equity Study 2016

CES
Start date: December 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the impact of a provider counseling training on patient contraceptive behaviors and satisfaction in a clustered randomized trial among 10 Planned Parenthood health centers.