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Expanded Program for Immunization, a Missed Opportunity for Postpartum Family Planning Utilization

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04780243
Enrollment
1474
Registered
2021-03-03
Start date
2020-02-01
Completion date
2021-03-17
Last updated
2021-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contraceptive Usage

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.

Interventions

OTHERcounseling

Mothers presented to infant immunization units are going to be counseled for family planning services and if decide to take any method, they will be linked to family planning services

Sponsors

Hawassa University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
After the initiation of the intervention, improved Contraceptive prevalence rate will be expected as an outcomethe outcome is measured two months after the initiation of the interventionAfter counseling of the postpartum mothers for family planning, their informed decision making capacity to use contraceptives will be increased.

Countries

Ethiopia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026