Actively Recruiting

Phase 2
All Genders
Healthy Volunteers
NCT04984551

Impact of Project ECHO on Improving the Quality of Palliative Care in Patients With Advanced Cancer and Their Caregivers in Underserved Areas of Kenya, Nigeria, Ghana, South Africa, India, and Ethiopia

Led by M.D. Anderson Cancer Center · Updated on 2026-03-05

312

Participants Needed

1

Research Sites

331 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This trial investigates the experience and satisfaction of care in patients with cancer that has spread to other places in the body (advanced) and their caregivers living in underserved areas of Kenya, Nigeria, Ghana, South Africa, India and Ethiopia as part of Project Extension for Community Healthcare Outcomes (ECHO). Project ECHO is a model of medical education and care management that empowers clinicians to provide better care to more people where they live. Understanding the experiences and satisfaction of patients and caregivers may help improve healthcare workforce capacity and increase access to specialty care for the world's rural and underserved populations.

CONDITIONS

Official Title

Impact of Project ECHO on Improving the Quality of Palliative Care in Patients With Advanced Cancer and Their Caregivers in Underserved Areas of Kenya, Nigeria, Ghana, South Africa, India, and Ethiopia

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient scheduled to receive treatment at participating primary care practice for advanced cancer
  • Patient is 18 years or older
  • Patient willing to be accessible to the research team for follow-up by telephone or in person
  • Patient has prognosis of at least 1 year as determined by treating physician
  • Patient able to read and understand English as assessed by treating physician
  • Caregiver identified or self-identified as primary caregiver of the patient
  • Caregiver willing to be accessible to the research team for follow-up by telephone or in person
  • Caregiver is 18 years or older
  • Caregiver able to read and understand English as assessed by treating physician
  • ECHO participant must be a healthcare provider interested in participating for 2 years and able to understand the protocol and provide consent
  • ECHO participant able to read and understand English as assessed by principal investigator
Not Eligible

You will not qualify if you...

  • Unable to understand and sign consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

M D Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

S

Sriram Yennu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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