BridgeMD
New treatment option for Short Interpregnancy Intervals
Official title Planning Together: A Couple-based, Multi-level Prenatal Contraceptive Education Program for Economically Marginalized Families
ClinicalTrials.gov ID: NCT07214012
What this study is testing
- What it's testing
- The goal of this pilot trial is to examine the feasibility and acceptability of the Planning Together protocol The hypothesis of this study are 1. The study will achieve feasibility, demonstrated by ≥80% study accrual (30 couples in 8 months), ≥75% protocol adherence, and ≥75% (e.g., education workbook completion) 2.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- Patient
- \> 20 weeks pregnant, age 18+
- The pregnant person has an available romantic partner, and the couple was able to get pregnant on their own or will be able to after the delivery
- separately, the pregnant person reports being in a sexually, psychologically and physically safe relationship
- English-speaking Romantic Partner
You likely can't join if
- Patient Exclusion Criteria:
- Participant is under the age of 18
- Documented cognitive impairment or psychiatric condition in pregnant person's medical record (e.g., severe learning disability, dementia, current...
- Participation in a concurrent contraceptive education intervention
- The pregnant person has a high-risk medical condition Romantic Partner Exclusion Criteria:
- Less than 18 years of age
See the full eligibility criteria
- Patient
- \> 20 weeks pregnant, age 18+
- The pregnant person has an available romantic partner, and the couple was able to get pregnant on their own or will be able to after the delivery
- separately, the pregnant person reports being in a sexually, psychologically and physically safe relationship
- English-speaking Romantic Partner
- 18 years of age and older
- Cohabiting with the patient; in a romantic relationship with patient
- Capable of getting the patient pregnant after delivery
- Does not need to be the biological father of the current pregnancy
- English-speaking (in order to take part in the interview as the interviewer does not speak Spanish)
- Patient Exclusion Criteria:
- Participant is under the age of 18
- Documented cognitive impairment or psychiatric condition in pregnant person's medical record (e.g., severe learning disability, dementia, current psychotic disorder, suicidality)
- Participation in a concurrent contraceptive education intervention
- The pregnant person has a high-risk medical condition Romantic Partner Exclusion Criteria:
- Less than 18 years of age
- Are not cohabiting with the patient; not in a romantic relationship with patient
- Not capable of getting the patient pregnant after delivery
The study team makes the final eligibility decision.
Where it's taking place
- Knoxville, Tennessee, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Knoxville, Tennessee, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.