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Tests a data-driven action model to help Indonesian district health leaders

Tests a data-based decision model for primary care in Indonesian districts.

Plain-language title generated from the registry record
Registry title: Scalable Public Health Empowerment, Research, and Education Sites (SPHERES)

Key facts

Where
Gerung and Purbalingga, IndonesiaSee the 2 sites

Where in Indonesia

  • West Lombok District Health OfficeGerung, IndonesiaNo longer taking part
  • Purbalingga District Health OfficePurbalingga, IndonesiaNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Oxford University Clinical Research Unit Indonesia
Trial code
NCT07126041
Record updated
15 August 2025
Original description
SPHERES is a health service research trial in the Indonesian primary care system designed to improve health system performance using a structured data-driven action model. The intervention empowers district health leaders to make data-informed decisions that will enhance outcomes across maternal, child, infectious, and non-communicable disease programs.Read full original descriptionShow less

End-to-end Digital Transformation for Primary Health Care Performance Management Via Scalable Public Health Empowerment, Research, and Education Sites: A Stepped-Wedge Cluster Randomized Trial

SPHERES is a health service research trial in the Indonesian primary care system designed to improve health system performance using a structured data-driven action model. The intervention empowers district health leaders to make data-informed decisions that will enhance outcomes across maternal, child, infectious, and non-communicable disease programs.

Inclusion: Residing in or participating in the district catchment areas; Receiving services from participating health care facilities; Health providers and district health officials consent to participate in data collection.

Exclusion: Inability to provide consent due to cognitive impairment or acute illness for health workers or district health officials involved in data collection; Individuals (health workers or patients) who decline to provide informed consent; Individuals who are not directly involved in or accessing services from health care facilities or district health offices.

ClinicalTrials.gov NCT07126041