Condition: Short Interpregnancy Intervals · Maternal Health Disparities · Sponsor: University of Tennessee Graduate School of Medicine
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.
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| University of Tennessee Graduate School of Medicine | Knoxville, Tennessee, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07214012