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Evaluating the Impact of a Symptom Checker on Healthcare-seeking Decisions: a Mixed-Methods Study

Safety and Feasibility of the Integration of Ada Into the Mobile MomConnect Information Service for Pregnant Women and New Mothers in South Africa

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06790069
Acronym
SAFEMOM
Enrollment
968
Registered
2025-01-23
Start date
2023-05-04
Completion date
2023-08-15
Last updated
2025-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Maternal Health Care

Keywords

maternal health, mobile health tools, symptom checker

Brief summary

The goal of this study is to evaluate the integration of a symptom checker (SC) into the MomConnect (MC) platform to support maternal healthcare in South Africa. The main questions it aims to answer are: * Does the SC provide safe and appropriate medical advice? * Does the SC help mothers make informed decisions about when and where to seek healthcare, saving time and money by avoiding unnecessary visits? * Does the SC improve access to care for those facing significant healthcare barriers? Participants will answer survey questions before and after using the SC. A subset of participants will also be invited to participate in structured telephone interviews. The study will help researchers assess the SC's impact on healthcare decisions and resource use in South Africa.

Interventions

None listed

Sponsors

Reach Digital Health (formerly Praekelt.org)
CollaboratorUNKNOWN
Citizen Surveys
CollaboratorUNKNOWN
Rockefeller Foundation
CollaboratorOTHER
Ada Health GmbH
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
OTHER

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Women registered with MomConnect, who would like to assess their or their child's symptoms * At least 18 years of age * Women with access to WhatsApp * Capable of completing a symptom assessment in English

Exclusion criteria

* Incapable of completing a symptom assessment in English via WhatsApp (e.g. due to illiteracy, language barrier, mental impairment or inebriation or other incapacity or lack of access to WhatsApp)

Design outcomes

Primary

MeasureTime frame
Proportion of appropriate advice by the SC for mother and childFrom data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.
Proportion of safe advice by the SC for mother and childFrom data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.

Secondary

MeasureTime frame
Health seeking behaviour before and after using Ada+MomConnectFrom data collection with participant enrolment to the completion of the follow-up survey send out 1 week after enrolment.
Gaining of health information in a fast and standardised wayOn the day of enrolment.
UsabilityOn the day of enrolment.
Time saved from avoiding unnecessary healthcare consultationsOn the day of enrolment.
Time saved and associated estimate of income retained through avoiding unnecessary healthcare consultationsOn the day of enrolment.
Healthcare resource utilisationOn the day of enrolment.
Direct Healthcare costsOn the day of enrolment.
Potential prevention of a health problem in Perinatal Period for Mother or ChildFrom data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.
Potential prevention of a SEVERE health problem in Perinatal Period for Mother or ChildFrom data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.
Potential Occurrence of a health problem (adverse event) in Perinatal Period for Mother and ChildFrom data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.
Potential Occurrence of a SEVERE health problem (severe adverse event) in Perinatal Period for Mother or ChildFrom data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment.
Number of participants who consulted an HCP after using Ada+MomConnectAfter completion of the follow-up survey send out 1 week after enrolment.

Other

MeasureTime frame
Time to receiving adviceOn the day of enrolment.
Time to diagnosisFrom data collection with participant enrolment to the completion of the follow-up survey send out 1 week after enrolment.
Quantitative and qualitative information collected in the phone survey on demographics, health seeking behaviour and user experience with the symptom checkerApprox. 1-2 weeks after enrolment.
Condition comparisonOn the day of enrolment.
Socioeconomic background of usersOn the day of enrolment.
Subgroup analysisFrom data collection with participant enrolment to the completion of panel ratings, approximately 2-3 months after participant enrolment

Countries

South Africa

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 18, 2026