AfyaJamii (Parenting Well): Evaluating the Feasibility of a Group Antenatal/Well-child Care Model in Pregnancy in Kenya

June 14, 2017 updated by: Astrid Christoffersen-Deb, Moi University

AfyaJamii (Parenting Well): Evaluating the Feasibility of a Group Antenatal and Well-child Care Model in Pregnancy in Kenya

This proposal is a program evaluation of a group care delivery model designed for pregnant women that was implemented as a pilot project in Teso District, Kenya in 2012.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The investigators will carry out a pre/post evaluation of this program comparing maternal and child health indicators collected at the facility and at 10 comparison facilities in the year prior to implementation (2012) and throughout the duration of the program (2013-2014). They will also analyze program attendance records, anonymous exit surveys, and training records.

Study Type

Interventional

Enrollment (Actual)

15

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Kocholya, Kenya
        • Teso North Ministry of Health Centers

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 50 years (Child, Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • All facilities that participated in AfyaJamii

Exclusion Criteria:

  • Any facility that did not offer AfyaJamii and was not been selected as a comparison facility

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: AfyaJamii facility
Facilities using AfyaJamii
AfyaJamii is a group antenatal and well-child care program developed in Kenya for use in Kenyan health centers
No Intervention: Referent facility
Facilities using Focused Antenatal Care Individual Model

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Facility 4 Antenatal Care (ANC) visits
Time Frame: 18 months
Average monthly number 4 or more ANC facility visits
18 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Facility New Family Planning (FP)
Time Frame: 18 months
Average monthly number new FP visits
18 months
Facility Total FP
Time Frame: 18 months
Average monthly number total FP visits
18 months
Facility Delivery Rate
Time Frame: 18 months
Average monthly number of Facility deliveries
18 months
Facility Oral Polio Vaccine 0 (OPV0)
Time Frame: 18 months
Average monthly number of OPV0 Immunization
18 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Collaborators

Investigators

  • Principal Investigator: Julia Songok, MBChB, Moi University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2012

Primary Completion (Actual)

October 1, 2014

Study Completion (Actual)

October 1, 2014

Study Registration Dates

First Submitted

May 31, 2017

First Submitted That Met QC Criteria

June 14, 2017

First Posted (Actual)

June 15, 2017

Study Record Updates

Last Update Posted (Actual)

June 15, 2017

Last Update Submitted That Met QC Criteria

June 14, 2017

Last Verified

June 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • UMoi2

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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