Understanding factors affecting postpartum contraception and pregnancy spacing
Patient, Partner, and Provider Determinants of Postpartum Contraception and Inter-Pregnancy Intervals
This study is looking at what helps or stops new moms from using birth control after having a baby, so they can better plan their next pregnancy and stay healthy.
Quick facts
| Grant type | R01 grant |
|---|---|
| Study type | NIH-funded research |
| Funding institution | Northwestern University at Chicago NIH-funded |
| Lab location | 1 site (Chicago, United States) |
| Project ID | NIH-11067451 on NIH RePORTER |
What this research studies
This research investigates the factors that influence postpartum contraception use and the timing between pregnancies. It aims to identify barriers that prevent patients from receiving adequate postpartum care and counseling, particularly focusing on the psychosocial and behavioral aspects that may affect contraceptive choices. By analyzing patient, partner, and provider determinants, the study seeks to improve awareness and access to effective contraception options for postpartum patients. The ultimate goal is to reduce the risks associated with short interpregnancy intervals, such as preterm delivery and low birth weight.
Who could benefit from this research
Good fit: Ideal candidates for this research are postpartum individuals who have recently given birth and are considering their options for contraception and future pregnancies.
Not a fit: Patients who are not postpartum or those who have no interest in future pregnancies may not benefit from this research.
Why it matters
Potential benefit: If successful, this research could lead to improved postpartum care and better health outcomes for mothers and infants by promoting effective contraception and optimal pregnancy spacing.
How similar studies have performed: Previous research has shown that addressing barriers to postpartum care and enhancing contraceptive counseling can lead to better health outcomes, indicating that this approach has potential for success.
Where this research is happening
Chicago, United States
- Northwestern University at Chicago — Chicago, United States (Active)
Researchers
- Principal investigator: Bailey, Stacy C — Northwestern University at Chicago
- Study coordinator: Bailey, Stacy C
About this research
- This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
- Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
- For full project details, budget, and progress reports, visit the official NIH RePORTER page below.