- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06654505
Can Village Health Volunteers/Workers Working As Male-Female Pairs Improve the Use of Postnatal Care Services in the Lao People's Democratic Republic
Effectiveness of Village Health Volunteers/Workers Working As Male-Female Pairs on Women's Use of Postnatal Care Services in Sepone District in Lao People's Democratic Republic: a Protocol for a Quasi-experimental Cluster Study
The study aims to assess the effectiveness of male-female VHV/Ws working in pairs on women's uptake of second PNC visits in rural Sepone, Lao PDR.
Methods A quasi-experimental cluster study will be conducted between July 2024 and October 2026 in 37 selected sites from two districts in southern Lao PDR. In 19 selected intervention villages in the Sepone district, female-male VHV/Ws pairs will promote postpartum services, whereas, in 18 similar control villages in the Vilabuly district, VHV/Ws will work as individuals.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Credo Ahissou, PhD
- Phone Number: +818064827518
- Email: Adelphahiss@gmail.com
Study Locations
-
-
-
Savannakhet, Lao People's Democratic Republic
- Recruiting
- Sepon and Vilabouly districts
-
Contact:
- Tiengkham PONGVONGSA
- Phone Number: +8562055640403
- Email: tiengkhampvs@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Women who gave birth within six weeks and twelve months before the study's baseline and end-line surveys.
Exclusion Criteria:
- Women whose births resulted in a loss,
- Women who do consent to participate in the surveys
- Women who face a language barrier with surveyors will not be enrolled.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Villages where Village Health Volunteers/Workers work as individuals
|
|
|
Experimental: Villages where Community Health Workers work in pairs
|
Community Health Workers will promote maternal and child health services as paired female and male
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Uptake of second postnatal care visit
Time Frame: 6 weeks after delivery
|
Second postnatal visit within 6 weeks after delivery in a health facility reported in maternal and child health handbook
|
6 weeks after delivery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lenght of facility-based postpartum stay
Time Frame: cutoff is 12 hours
|
Number of hours of stay in health facility after delivery
|
cutoff is 12 hours
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 24-2329-00-00-00
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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