- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03188237
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
Conditions
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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