NCT07214012 Planning Together: A Couple-based, Multi-level Prenatal Contraceptive Education Program for Economically Marginalized Families
| NCT ID | NCT07214012 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Tennessee Graduate School of Medicine |
| Condition | Short Interpregnancy Intervals |
| Study Type | INTERVENTIONAL |
| Enrollment | 60 participants |
| Start Date | 2025-11-25 |
| Primary Completion | 2026-10-14 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 60 participants in total. It began in 2025-11-25 with a primary completion date of 2026-10-14.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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. The intervention will be acceptable, with \>80% of participants reporting satisfaction with Planning Together. 3. Patterns of primary outcomes (contraceptive knowledge, communication quality, community referral utilization) and secondary outcomes (agreed contraceptive plan, consistent contraceptive usage and satisfaction, psychological distress, and Short Interpregnancy Intervals \[SII\]) will suggest benefits of the intervention.
Eligibility Criteria
Inclusion Criteria: Patient Inclusion Criteria: 1. \> 20 weeks pregnant, age 18+ 2. 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 3. separately, the pregnant person reports being in a sexually, psychologically and physically safe relationship 4. English-speaking Romantic Partner Inclusion Criteria: 1. 18 years of age and older 2. Cohabiting with the patient; in a romantic relationship with patient 3. Capable of getting the patient pregnant after delivery 4. Does not need to be the biological father of the current pregnancy 5. English-speaking (in order to take part in the interview as the interviewer does not speak Spanish) Exclusion Criteria: Patient Exclusion Criteria: 1. Participant is under the age of 18 2. Documented cognitive impairment or psychiatric condition in pregnant person's medical record (e.g., severe learning disability, dementia, current psychotic disorder, suicidality) 3. Participation in a concurrent contraceptive education intervention 4. The pregnant person has a high-risk medical condition Romantic Partner Exclusion Criteria: 1. Less than 18 years of age 2. Are not cohabiting with the patient; not in a romantic relationship with patient 3. Not capable of getting the patient pregnant after delivery
Frequently Asked Questions
Who can join the NCT07214012 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Short Interpregnancy Intervals. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07214012 currently recruiting?
Yes, NCT07214012 is actively recruiting participants. Visit ClinicalTrials.gov or contact University of Tennessee Graduate School of Medicine to inquire about joining.
Where is the NCT07214012 trial being conducted?
This trial is being conducted at Knoxville, United States.
Who is sponsoring the NCT07214012 clinical trial?
NCT07214012 is sponsored by University of Tennessee Graduate School of Medicine. The trial plans to enroll 60 participants.
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