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Clinical Trials/NCT04780243
NCT04780243
Unknown
Not Applicable

Enhancing Postpartum Family Planning Utilization Through Integration With Expanded Program for Immunization in Sidama, South Ethiopia: A Quasi Experimental Study

Hawassa University1 site in 1 country1,474 target enrollmentFebruary 1, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Contraceptive Usage
Sponsor
Hawassa University
Enrollment
1474
Locations
1
Primary Endpoint
After the initiation of the intervention, improved Contraceptive prevalence rate will be expected as an outcome
Last Updated
5 years ago

Overview

Brief Summary

This study is aimed to enhance postpartum family planning by integrating family planning information with infant immunization services, which is the most widely utilized health services globally.

Detailed Description

In this study, a before-and-after type of quasi-experimental study will be conducted in purposely selected health centers Sidama region, Ethiopia. base line assessment of postpartum contraceptive utilization rate will be done which will be followed by an intervention. The intervention consists of screening, counseling for family planning and referring mothers coming for infant immunization services to family planning units. All mothers coming for infant immunization service will be screened for and counseled for family planning and those who will be voluntary to take any method will be referred to family planning unit. All mothers who will not be voluntary will be re-counseled by the next visit. Finally, the effect of this intervention on postpartum contraceptive utilization rate will be reassessed. The expected outcome will be to see an improved contraceptive uptake during the first year after delivery.

Registry
clinicaltrials.gov
Start Date
February 1, 2020
End Date
March 17, 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Sequential
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Abebaw Abeje Muluneh

Mr.

Hawassa University

Eligibility Criteria

Inclusion Criteria

  • all women visiting health facilities for infant immunization for at least two times will be included.

Exclusion Criteria

  • Women who are in difficulty of communicating during the study period will be excluded.

Outcomes

Primary Outcomes

After the initiation of the intervention, improved Contraceptive prevalence rate will be expected as an outcome

Time Frame: the outcome is measured two months after the initiation of the intervention

After counseling of the postpartum mothers for family planning, their informed decision making capacity to use contraceptives will be increased.

Study Sites (1)

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