NCT06304831

Brief Summary

Despite increasing options for public and private health care providers in Laos, choosing a high-quality health provider or a facility is difficult because timely and reliable information about providers is not readily available. People rely on social networks or previous experiences to select providers. However, in Laos, only 28% describe their recent visit to a health care provider as high-quality suggesting that while there are increasing options for care, people may need support to find providers that meet their quality needs. Rapid adoption of mobile phones in Laos, particularly in urban areas, offer opportunities to enhance people's access to timely quality information about health care providers. The study team will use mobile phones to collect and disseminate quality information about providers - known to be valued by Laotians - to improve their access to quality care as well as their overall satisfaction with care.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
559

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 5, 2024

Completed
6 days until next milestone

Study Start

First participant enrolled

March 11, 2024

Completed
1 day until next milestone

First Posted

Study publicly available on registry

March 12, 2024

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 23, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 23, 2024

Completed
Last Updated

January 13, 2025

Status Verified

March 1, 2024

Enrollment Period

8 months

First QC Date

March 5, 2024

Last Update Submit

January 9, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Proportion of mothers that change their preferred health care providers for children for non-urgent care

    The primary outcome of this study is the proportion of mothers that changed their preferred health care facility for non-urgent child care services between baseline and endline surveys. Non-urgent care is defined as children with mild fever of 38 degrees along with cough. During the baseline and endline surveys, participants will be asked to specify their preferred location for non-urgent child care as follows: "If your child is sick tomorrow with mild fever of 38 degrees Celsius and cough, which hospital, clinic or health center will you take your child to?" The primary outcome will be a binary indicator for participants changing their preferred location between baseline and endline.

    3 months

Secondary Outcomes (6)

  • Proportion of mothers satisfied with health care for their children of their most recent visit

    3 months

  • Number and type of health care providers used in the past 3 months

    3 months

  • Proportion of mothers that change their most recently visited health care providers for children

    3 months

  • Proportion of mothers choosing the preferred facility for non-urgent care because of online or digital information sources

    3 months

  • Proportion of mothers that change their preferred health care providers for children for urgent care

    3 months

  • +1 more secondary outcomes

Study Arms (2)

Intervention

EXPERIMENTAL

The intervention group will receive biweekly updates about quality ratings of recently visited health care providers for children by everyone enrolled in the study.

Behavioral: Quality ratings of health care providers for children

Control

NO INTERVENTION

The control group will not receive any information about health care providers for children.

Interventions

Ratings of overall and components of quality (provider knowledge, respectfulness of provider, respectfulness of staff, cleanliness, cost) of health care providers for children will be provided on a webpage. The webpage will be updated every week and participants will be invited to access the latest ratings biweekly.

Intervention

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • All women 18 years of age and older and enrolled in Vientiane Multigenerational Birth Cohort (VITERBI) with at least one child less than two years old, able to read, have exclusive access to a mobile phone, have a WhatsApp account, understand and sign the ICF will be eligible to participate in the study. The eligibility criteria will be assessed using data collected from VITERBI. Ability to read will be tested using a script in Lao, "I use my mobile phone every day."

You may not qualify if:

  • Eligible women unwilling to sign informed consent, without exclusive access to a mobile phone, unable to read the test script, or unable operate a mobile phone will be excluded from the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Lao Tropical and Public Health Institute

Vientiane, Vientiane Capital, Laos

Location

Related Publications (1)

  • Aryal A, Clarke-Deelder E, Sayasone S, Fink G. Informing Facility Selection Through a Web-Based User Ratings System: Protocol for a Randomized Controlled Trial Among Mothers in Urban Lao People's Democratic Republic. JMIR Res Protoc. 2025 Sep 4;14:e66085. doi: 10.2196/66085.

Study Officials

  • Günther Fink, PhD

    Swiss Tropical & Public Health Institute

    STUDY CHAIR
  • Amit Aryal, MPH

    Swiss Tropical & Public Health Institute

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Model Details: This study consists of a randomized controlled experiment involving 660 mothers with children less than 2 years old. Participants will be randomly assigned to one of two groups: 1) a control group that will not receive any information about providers and 2) an intervention group that will receive biweekly updates about quality ratings based on reviews collected from mothers of young children in the study areas. The unit of randomization will be the individual participant. A simple random number draw generated by the ODK package installed on the tablets will be used to assign participants to treatment and control with equal probability.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 5, 2024

First Posted

March 12, 2024

Study Start

March 11, 2024

Primary Completion

October 23, 2024

Study Completion

October 23, 2024

Last Updated

January 13, 2025

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will not share

De-identified survey data will be retained for at least 15 years on a public data repository after publication of study findings.

Locations