Menu
Recruiting 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

No phase Interventional Pregnant Women Lactating Mother

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Paired Community Health Workers.
Who it may be relevant to
Registry conditions: Pregnant Women, Lactating Mother. Basic parameters: 15 years — 49 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Laos
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Interventions

  • Behavioral Paired Community Health Workers
    Community Health Workers will promote maternal and child health services as paired female and male

Primary outcome measures

  • Uptake of second postnatal care visit [Time frame: 6 weeks after delivery]
Secondary outcome measures (1)
  • Lenght of facility-based postpartum stay [Time frame: cutoff is 12 hours]

Eligibility criteria

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.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Health services research

Study locations

Laos · 1 center
  • Sepon and Vilabouly districts — Savannakhet

Identifiers

NCT: NCT06654505 · 24-2329-00-00-00

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗