Can Village Health Volunteers/Workers Working As Male-Female Pairs Improve the Use of Postnatal Care Services in the Lao People's Democratic Republic

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age15-49
SponsorUniversity of the Ryukyus

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Women who gave birth within six weeks and twelve months before the study's baseline and end-line surveys.

Disqualifiers

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.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Paired Community Health Workers

    Behavioral

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

Treatment groups

302 Participants
are divided into 2 treatment groups
Group A: Villages where Village Health Volunteers/Workers work as individualsNo intervention 0 interventions
Group B: Villages where Community Health Workers work in pairsExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Uptake of second postnatal care visit

Second postnatal visit within 6 weeks after delivery in a health facility reported in maternal and child health handbook

Time frame
6 weeks after delivery

Secondary outcomes

1

Lenght of facility-based postpartum stay

Number of hours of stay in health facility after delivery

Time frame
cutoff is 12 hours

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.