Effectiveness of a package of postpartum family planning interventions on the uptake of contraceptive methods until 9 months postpartum in Burkina Faso

Not Applicable

• Conditions: Postpartum family planning

• Registration Number: PACTR201609001784334
• Lead Sponsor: Department of Reproductive Health Research, World Health Organization, Geneva, Switzerland

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-09-17
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Complete
• Sex: Female
• Target Recruitment: 560

Inclusion Criteria

All pregnant women will be eligible to participate in the intervention phase of the study if (1) they are in their third pregnancy trimester; (2) the status of the pregnancy and of the woman allows for a birth at the health center; (3) the woman has the intention to attend ANC, delivery and PNC at the health center; (4) the woman does not participate in another study; and (5) an informed consent is obtained.

Exclusion Criteria

All pregnant women that will not be eligible to participate in the intervention phase of the study if (1) they are not in their third pregnancy trimester; (2) the status of the pregnancy and of the woman do not allow for a birth at the health center; (3) the woman has not the intention to attend ANC, delivery and PNC at the health center; (4) the woman does participate in another study; and (5) an informed consent is not obtained.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome is the uptake of a modern contraceptive method at nine months postpartum.

Secondary Outcome Measures

Name	Time	Method
Intention to use a contraceptive method, and decision made to use a contraceptive method;Use of a modern contraceptive method