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ePartogram Effectiveness Study in Kenya

NCT03757598 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 113

Last updated 2019-12-11

No results posted yet for this study

Summary

Quasi-experimental study to evaluate whether clinical care offered to clients was more appropriate and in line with WHO recommendations for care in normally progressing labor and in labor with complications, among providers using the novel intervention, ePartogram (an electronic version of the WHO paper partograph) vs. providers who offered care using the standard paper partograph, and whether fetal/newborn outcomes were improved among cases where partograph was used.

Conditions

  • Obstetric Complication
  • Obstetric Labor Complications
  • Newborn Morbidity

Interventions

OTHER

ePartogram use

Electronic partograph based on WHO standard paper partograph is given in Android tablet used by provider monitoring clients in labor. Providers had received training in using the ePartogram and ongoing trouble shooting.

Sponsors & Collaborators

  • GE Healthcare

    collaborator INDUSTRY

  • Jhpiego

    lead OTHER

Principal Investigators

  • Sanghvi Harshad, MD · Jhpiego

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-08-01
Primary Completion
2017-05-30
Completion
2017-05-30

Countries

  • Kenya

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03757598 on ClinicalTrials.gov