Understanding postpartum contraception practices and attitudes
Regular Six Weeks Versus Earlier Postpartum Initiation of Long-acting Reversible Contraceptives: Knowledge Attitude and Practice Study (KAP)
This study looks at how new moms and healthcare providers feel about starting long-lasting birth control right after having a baby to see if starting it sooner is better for their health.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 600 (estimated) |
| Ages | 18 Years to 60 Years |
| Sex | All |
| Sponsor | Assiut University Academic / other |
| Locations | 1 site (Assiut) |
| Trial ID | NCT06273670 on ClinicalTrials.gov |
What this trial studies
This observational study aims to compare the knowledge, attitudes, and practices of clients and service providers regarding the initiation of long-acting reversible contraceptives (LARC) during the postpartum period. Utilizing structured questionnaires in both English and Arabic, the study will gather data from family planning centers in public health facilities. The focus is on understanding the differences between regular initiation at six weeks versus earlier initiation of LARC methods. The findings could inform better practices in postpartum family planning and improve maternal health outcomes.
Who should consider this trial
Good fit: Ideal candidates include postpartum women attending family planning centers who are either using or willing to use LARC methods.
Not a fit: Patients currently using or willing to use contraceptive methods other than LARC may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance postpartum contraceptive practices, leading to reduced maternal and infant mortality rates.
How similar studies have performed: Other studies have shown that improved knowledge and access to postpartum contraception can significantly enhance maternal health outcomes, indicating a promising approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Client's group All clients who were attending family planning centers in public health facilities at the study period if they have had a postpartum LARC method (Copper IUD, Progestin-releasing IUS, Subdermal implant) or willing to use it in the first year after delivery. Service provider group: All service providers who are working in primary health care units \& hospitals, including general practitioners, ob/gyn. specialists, nurses, and social workers. Exclusion Criteria: * Clients and service providers who refused to participate in the study * Clients who are currently using or willing to use a method other than LARC
Where this trial is running
Assiut
- Assiut University — Assiut, Egypt (Recruiting)
Study contacts
- Study coordinator: Nada M. Khalil, Diploma
- Email: Topspot55@gmail.com
- Phone: +201146640044
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.