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NCT03888404 · ClinicalTrials.gov registry record
Attitudes and Decision-making After Pregnancy Testing Study
A clinical trial of Unintended Pregnancy and Undesired Pregnancy, sponsored by University of California, San Francisco.
- Active
- Registry status
- 2,015
- Enrollment target
- 1
- Study location
NCT03888404: Active study of Unintended Pregnancy and Undesired Pregnancy, sponsored by University of California, San Francisco.
NCT03888404 is a study of Unintended Pregnancy and Undesired Pregnancy that is active but no longer recruiting, run by University of California, San Francisco. The registered enrollment target is 2,015 participants. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03888404, a study of Unintended Pregnancy and Undesired Pregnancy, is active but no longer recruiting, sponsored by University of California, San Francisco.
- ACTIVE NOT RECRUITING
- Registry status
- 2,015 participants
- Enrollment target
- 1
- Study location
Study Summary
The ADAPT Study is a longitudinal observational cohort study examining women's pregnancy preferences, pregnancy decision-making processes, and the effects of less preferred (commonly called "unintended") pregnancy on women's lives. This study will enroll and follow prospectively an Underlying Cohort (UC) of women who are not pregnant at baseline. The study will measure the degree to which participants desire to avoid pregnancy multiple times over the course of the year and capture incident pregnancies as they occur over time. Participants experiencing new pregnancies during the one-year UC will be transferred into a new cohort, the Pregnancy and Match Cohort (PMC); these women will be followed over the course of their pregnancy decision-making and health care-seeking to document these processes. In addition, they will be followed through their pregnancies and giving birth to investigate differences in health, well-being, and socioeconomic outcomes associated with carrying a pregnancy to term based on the participant's pre- and post-pregnancy preference about the pregnancy. Finally, a cohort of non-pregnant women from the UC, matched on desire to avoid pregnancy and time at risk of pregnancy, will be followed as part of the PMC. The study will compare the health, well-being, and socioeconomic outcomes of women with new pregnancies and new births to those in the non-pregnant group to assess the effect of pregnancy itself on women. The ADAPT study has the following aims: Aim 1: Assess the factors associated with women's pregnancy preferences, how preferences change over time, and their associations with contraceptive use, incident pregnancy, and feelings about the pregnancy after discovery (Underlying Cohort) Aim 2: Investigate the options that women consider when they become pregnant and the factors that influence their pregnancy decision-making and ability to access desired reproductive health care and services (prenatal, abortion, adoption) (Study A) Aim 3a: Exa
Primary Outcome
The Perceived Stress Scale (PSS) measures stress; scores are summed across 4 scale items (brief version), each with responses never to very often, on a 5-point scale, for a score ranging 0-16. The outcome will be the predicted mean PSS score over the 8 PMC survey observations (a single measure of effect), based on the marginal effect from a longitudinal multivariable mixed effects model.
Conditions Studied
Interventions
- OTHER Pregnancy preferences (Aim 1)
- OTHER Sociocultural environment (Aim 2)
- OTHER Pregnancy preferences (Aim 3a)
- OTHER Pregnancy (Aim 3b)
Study Locations (1)
California
- University of California, San Francisco - Oakland
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,015 participants |
| Start Date | 2019-03-16 |
| Est. Completion | 2026-06 |
What the registry record for NCT03888404 still lists
NCT03888404 is an observational study that tracks outcomes without assigning an intervention. Its 2,015 participants enrollment target places it among the larger protocols in the corpus.
The record links to 2 conditions, with Unintended Pregnancy appearing as the primary indexed condition, and to 4 interventions - of which Pregnancy preferences (Aim 1) is the first listed.
NCT03888404 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT03888404 about?
NCT03888404 is a clinical study titled "Attitudes and Decision-making After Pregnancy Testing Study". The ADAPT Study is a longitudinal observational cohort study examining women's pregnancy preferences, pregnancy decision-making processes, and the effects of less preferred (commonly called "unintended") pregnancy on women's lives. This study will enroll and follow prospectively an Underlying Cohort...
What is the current status of trial NCT03888404?
This trial is currently active not recruiting. The enrollment target is 2,015 participants. The study started on 2019-03-16. Estimated completion is 2026-06.
What conditions does trial NCT03888404 study?
This clinical trial studies the following conditions: Unintended Pregnancy, Undesired Pregnancy.
What interventions are being tested in trial NCT03888404?
The interventions under investigation include: Pregnancy preferences (Aim 1) (OTHER), Sociocultural environment (Aim 2) (OTHER), Pregnancy preferences (Aim 3a) (OTHER), Pregnancy (Aim 3b) (OTHER).
Who is sponsoring clinical trial NCT03888404?
This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03888404 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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