Contraception Behavior

8

Review clinical trials related to Contraception Behavior. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

"Vasectomy: Right for Me?" Decision Support Tool

The goal of this trial is to learn if a web-based decision aid designed to provide evidence-based information about vasectomy and other birth control options helps improve users' decision-making about birth control. The main questions it aims to answer are: * Do people who use the decision aid have better knowledge about vasectomy? * Do people who use the decision aid have lower conflict with their decision? Participants will: * Use the decision aid (if they are assigned to the intervention arm). * Answer survey questions about their knowledge, decision-making, interest in vasectomy, and healthcare navigation experiences.

Participants needed: 750
Trial details
Age: 21-55Biological sex: MaleType: InterventionalSponsor: University of PittsburghUpdated: Jul 1, 2026Locations: 2
Eligibility criteria

Are assigned male at birth [+5]

Are not assigned male at birth [+6]

Status: Recruiting

CARRII Native Intervention Optimization Trial

The purpose of this study is to identify the best combination of new intervention components to use with CARRII, the first automated online intervention for alcohol-exposed pregnancies (AEP). This intervention is specifically designed for Native women and others who can become pregnant. Our goal is to maximize the effectiveness of the online intervention while keeping costs manageable for Native communities.

Participants needed: 512
Trial details
Age: 18-44Biological sex: FemaleType: InterventionalSponsor: University of VirginiaUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Native American/American Indian/Alaska Native, [+3]

cognitive disorders including mental retardation, dementia, or psychotic disorde...

Status: Recruiting

Patient-centered Information on Permanent Contraception

The goal of this study is to understand whether providing information to women with a strong desire to avoid future pregnancy about how tubal sterilization compares to long-acting reversible contraceptives improves perceived access to available contraceptives. Participants will: * Complete a baseline survey * Receive access to web-based educational resources * Complete a brief follow up survey immediately after exploring these web-based resources * Complete a follow-up survey 3 months after enrolling The investigators will compare outcomes among participants provided with access to a new website (intervention) summarizing recent patient-centered outcomes research (PCOR) comparing interval laparoscopic tubal sterilization and long-acting reversible contraception (LARC) to control participants provided with access to the existing Planned Parenthood website on tubal sterilization.

Participants needed: 650
Trial details
Age: 21-45Biological sex: FemaleType: InterventionalSponsor: University of California, San FranciscoUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

Self-reported fertility [+2]

Current pregnancy [+5]

Status: Recruiting

Effectiveness Testing of a Videogame Intervention (No Baby No) to Decrease Contraception Non-use Among Adolescents.

The purpose of this study is to evaluate the effectiveness of a videogame compared to an attention/time control at reducing contraceptive non-use among adolescents.

Participants needed: 850
Trial details
Age: 15-20Biological sex: AllType: InterventionalSponsor: Weill Medical College of Cornell UniversityUpdated: Dec 22, 2025Locations: 7
Eligibility criteria

Male or Female [+3]

Age less than 15 or older than 20 [+2]

Status: Recruiting

Transdermal Ethinyl Estradiol and Norelgestromin for Irregular Bleeding in Contraceptive Implant Users

The goal of this clinical trial is to evaluate the effectiveness of transdermal contraceptive patches in treating irregular vaginal bleeding in women over 18 years old who are using contraceptive implants and experiencing abnormal vaginal bleeding. The main questions it aims to answer are: * Does transdermal ethinyl estradiol and norelgestromin patch effectively treat irregular vaginal bleeding caused by contraceptive implants compared to placebo? * What proportion of participants will report cessation of vaginal bleeding during treatment and remain bleeding-free at day 14 of treatment? * What is the safety profile and adherence rate of the transdermal patch treatment? Researchers will compare participants receiving active hormonal patches (ethinyl estradiol 600 mcg + norelgestromin 6 mg) to those receiving placebo patches to see if the hormonal treatment effectively stops irregular vaginal bleeding. Participants will: * Apply transdermal patches for 21 days (changing patch every 7 days - total of 3 patches) * Attend follow-up visits at days 7, 14, 21, and 3 months (day 14 in-person, others via telephone) * Complete bleeding diaries and report any side effects * Follow-up schedule: Day 7: Telephone follow-up to assess bleeding pattern, side effects, and patch adherence Day 14: In-person visit at the clinic for comprehensive evaluation including bleeding assessment, side effects monitoring, and adherence check Day 21: Telephone follow-up to evaluate treatment completion, ongoing bleeding status, and need for additional treatment 3 months: Final telephone follow-up to assess long-term outcomes and recurrence of bleeding

Participants needed: 40
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Chulalongkorn UniversityUpdated: Dec 10, 2025Locations: 1
Eligibility criteria

Women aged 18 years and older [+4]

Previous treatment for irregular vaginal bleeding within the past 3 months [+5]

Status: Recruiting

SAPLAI : Assessing the faiSAbility of a Peer-to-peer Contraceptive Education Program on Social Networks Aimed at 15- to 19-year-old High School Students in GuAdeloupe and La RéunIon

The goal of this clinical trial is to evaluate the feasibility of a contraception education program delivered by peers via social networks to high school students. Our primary hypothesis is that the implementation of a peer-led contraceptive education program via social networks is a feasible approach in high schools on Reunion Island and Guadeloupe, as part of a before-and-after study. Our secondary hypotheses concern the evaluation of adoption, exploratory efficacy (on knowledge, attitudes and practices), acceptability and fidelity of the peer-led education program via social networks among high school students in La Réunion and Guadeloupe. Participants will : * Participate in a focus group to explore their views and experiences regarding the value of a peer educator as a source of sexual and reproductive health information. * answer questionnaires on their knowledge of sexual health * A selected group (peer influencers): Create educational content (after a training period) on sexual health, and particularly contraception, to be broadcast on social networks. * Take note of the program distributed on the networks by the peer influencers (for 3 months) * Fill in questionnaires on their knowledge of sexual health, after the program.

Participants needed: 120
Trial details
Age: 15-19Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Universitaire de la RéunionUpdated: Jun 4, 2025Locations: 2
Eligibility criteria

HIGH SCHOOL STUDENTS [+15]

Status: Recruiting

Evaluation of Parent Toolkit 2.0 (Morehouse Family Health Study)

Child Trends will conduct a randomized control trial evaluation of Parent Toolkit 2.0, an innovative intervention for parents and caregivers of middle and high school students. Child Trends will collaborate with Morehouse School of Medicine and Tressa Tucker \& Associates, LLC to implement and evaluate the program with 1,000 parent-teen pairs across Georgia. The program includes three components that will be delivered across a three-week period: (1) an online self-paced Parent Guide with information, tips, tools, and resources on adolescent health, including sexual health; (2) four videos modeling parent-teen communication around sex and contraception; and (3) two group-based sessions for parent participants to discuss program content and improve communication skills. The program aims to increase parent knowledge and parent-teen communication about adolescent health, sexual health, and relationships to help youth adopt health-promoting behaviors such as delaying sexual initiation and increasing contraceptive use.

Participants needed: 2,000
Trial details
Age: 12-15Biological sex: AllType: InterventionalSponsor: Child TrendsUpdated: Apr 30, 2025Locations: 1
Eligibility criteria

25 to 70 years old [+3]

Lives in a home with a child who is already enrolled in this study [+4]

Status: Recruiting

The Impact of Hormonal Contraceptive Use and Lifestyle Factors on Fracture Risk and Bone Quality in Young Female Adults

The study on hand is based on a cross-sectional design and aims to acquire 1) descriptive data on the physical state and health condition of female soldiers in the German armed forces. 2) a possible influence of different contraceptive methods as well as physical activity, body composition, strength, nutrition, and hemoglobin levels on bone health should be investigated.

Participants needed: 150
Trial details
Age: 18-35Biological sex: FemaleType: ObservationalSponsor: Bundeswehr University MunichUpdated: Sep 23, 2024Locations: 1
Eligibility criteria

18 - 35 years [+4]

for the bioelectrical impedance: electronic implants like defibrillator, pregnan...