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Improving Adherence to Postpartum Family Planning Guidance in Ghana

Not Applicable
Completed
Conditions
Contraception
Interventions
Other: Postpartum Family Planning Package
Registration Number
NCT04306029
Lead Sponsor
University of Pennsylvania
Brief Summary

Evaluating a Postpartum Family Planning Package (PPFP) in a Hybrid Type II implementation study with a stepped-wedge design.

Detailed Description

Our overarching goal is to enable providers to consistently offer and deliver highly effective postpartum family planning methods in accordance with international guidelines. Our primary objective in this research is to assess the implementation and effectiveness of the "Postpartum Family Planning Package (PFPP)," an implementation strategy that consists of the following components: 1) a provider training on contraceptive methods available in the immediate postpartum period, and techniques for their placement in the case of intrauterine devices and implants, with quarterly booster trainings, and 2) promotion of the WHO MEC/Postpartum Family Planning Compendium mobile application as a provider decision tool to aid in postpartum family planning counselling.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
2142
Inclusion Criteria
  • Providers who care for postpartum women on the inpatient postpartum ward, including midwives, nurses, residents, fellows, and consultant physicians.

Provider

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Exclusion Criteria
  • Students caring for postpartum patients on the postpartum ward.

Client Inclusion Criteria:

  • Women receiving antenatal care who have the potential to be admitted to the inpatient postpartum ward following delivery, or women admitted in the postpartum ward.

Client Exclusion Criteria:

  • None
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
Post-InterventionPostpartum Family Planning PackagePostpartum staff has received the "Postpartum Family Planning Package," which consists of provider education on contraceptive delivery in the immediate postpartum period and promotion of the WHO MEC/PFP Compendium mobile application.
Primary Outcome Measures
NameTimeMethod
Provider discussed all guideline-appropriate contraceptive methods as defined by World Health Organization Medical Eligibility Criteria (yes/no)During postpartum inpatient stay, prior to hospital discharge (approximately 2 days)
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Ga West Municipal Hospital

🇬🇭

Amasaman, Greater Accra, Ghana

Nsawam Goverment Hospital

🇬🇭

Nsawam, Eastern Region, Ghana

Maamobi Hospital

🇬🇭

Accra, Ghana

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