Caring for Providers to Improve Patient Experience Study Phase 2 in Migori County

NCT05019131 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 83

Last updated 2025-05-07

Study results available
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Summary

The activities described in this proposal are aimed at addressing health care provider stress and unconscious bias to improve quality of maternal health care, particularly related to the person-centered dimensions of care-i.e. care that is respectful and responsive to women's needs, preferences, and values. The investigators focus on health provider stress and unconscious bias because they are key drivers of poor-quality care that are often not addressed in interventions designed to improve quality of maternal health care. The investigators plan to (1) design an intervention that enables providers to identify and manage their stress and unconscious bias; (2) pilot the intervention to assess its feasibility and acceptability; and (3) assess preliminary effect of the intervention on: (a) provider knowledge, attitudes, and behaviors related to stress and unconscious bias; and (b) provider stress levels.

Conditions

  • Maternal Health
  • Mental Health
  • Healthcare Provider
  • Adverse Outcomes
  • Stress
  • Stress, Psychological
  • Stress, Emotional
  • Quality of Care
  • Burnout
  • Discrimination, Social

Interventions

BEHAVIORAL

Training

trainings to reduce conscious bias and stress

BEHAVIORAL

Peer support and mentorship

facilitated peer and mentorship opportunities

BEHAVIORAL

Leadership engagement

Engaged leadership at the county and facility levels

BEHAVIORAL

Embedded champions

Facilitate local champions to promote intervention

Sponsors & Collaborators

  • Kenya Medical Research Institute

    collaborator OTHER
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH
  • University of California, San Francisco

    lead OTHER

Principal Investigators

  • Patience Afulani, PhD, MD, MPH · University of California, San Francisco

Study Design

Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-16
Primary Completion
2022-06-24
Completion
2023-08-31

Countries

  • Kenya

Study Locations

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Entities

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 NCT05019131 on ClinicalTrials.gov