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Search / Trial NCT06085105

Caring for Providers to Improve Patient Experience (CPIPE) Trial

Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Oct 11, 2023

Trial Information

Current as of July 09, 2025

Enrolling by invitation

Keywords

Quality Of Care Kenya Providers Mental Health Burnout Stress Person Centered Care Discrimination Prejudice Unconscious Bias

ClinConnect Summary

The Caring for Providers to Improve Patient Experience (CPIPE) Trial is focused on improving the care that women receive during and after childbirth. Researchers are looking at how stress and unconscious bias among healthcare providers can affect the quality of maternal health care. By addressing these issues, the trial aims to create a more respectful and responsive healthcare environment that meets women's needs. The study will test a special program designed to help providers manage stress and reduce bias, while also examining how this can lead to better health outcomes for mothers and their babies.

To participate in this trial, women who have given birth within the last 12 weeks and healthcare providers working in maternal health for at least six months are eligible. Women must be at least 15 years old and able to give consent, while providers need to be 18 or older and committed to attending training sessions. Participants can expect to take part in surveys and training sessions that aim to improve their experiences and the care provided. This trial is currently active but not recruiting new participants, meaning they are not looking for additional people at this time.

Gender

ALL

Eligibility criteria

  • Women's survey
  • Eligibility criteria
  • 1. Women receiving care at the study facilities.
  • 2. Have given birth within the 12 weeks preceding the data collection.
  • 3. Capable and willing to provide informed consent.
  • 4. Age 15 or above, with individuals aged 15-17 meeting the criteria for emancipated minors as defined by Kenyan or Ghana law (pregnant or parenting, living apart from their parents or guardian; living separately with or without their parents or guardian's consent, regardless of duration; and, controlling their financial affairs regardless of the source of income).
  • Exclusion criteria
  • 1. Women who are too ill to participate or do not live within a feasible location if interviews are scheduled to be conducted in the community.
  • 2. Women who are younger than 15 years of age.
  • Provider's cohort
  • Eligibility criteria
  • 1. Healthcare providers working in maternal health units for at least 6 months at the time of data collection.
  • 2. Capable and willing to provide informed consent.
  • 3. Able and committed to attending the intervention training and follow up activities.
  • 4. Age 18 or above.
  • Exclusion criteria
  • 1. Healthcare providers planning to no longer be working at the facilities in the next six months, at the time of enrollment.

About University Of California, San Francisco

The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.

Locations

Navrongo, , Ghana

Migori, , Kenya

Patients applied

0 patients applied

Trial Officials

Patience Afulani, PhD, MD, MPH

Principal Investigator

University of California, San Francisco

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported