Acceptability and Feasibility of Interventions for Integrated Care of Chronic Kidney Disease With Other Long-term Health Conditions in Malawi: a Qualitative Study (Impso)

January 29, 2025 updated by: Liverpool School of Tropical Medicine

Understanding Risk Factors for Progressive Chronic Kidney Disease in Malawi to Inform Interventions for Earlier Detection ad Prevention (Impso Study)

The burden of chronic kidney disease (CKD) is rising globally, but disproportionately impacting on low- and middle-income countries (LMIC) including Malawi, which have the fewest resources to manage it. Furthermore, CKD is the leading cause of catastrophic health expenditure worldwide, largely due to the extremely high costs of kidney replacement therapy (KRT) for people with kidney failure. Access to KRT remains limited in many settings, including Malawi, where there is only one nephrologist for a population of over 21 million. It is therefore essential to diagnose and treat CKD in its early stages, to facilitate earlier and more cost-effective treatment to prevent its progression to advanced disease which is associated with increased risks of kidney failure and of cardiovascular morbidity and mortality. CKD is usually asymptomatic in its early stages, so early diagnosis and treatments requires access to key diagnostic tests, in addition to strategies for channelling resources to those at the highest risk.

The causes of CKD are diverse, particularly in LMIC settings where the increasing prevalence of non-communicable diseases intersects with ongoing high burdens of infectious diseases, malnutrition, and many other social and environmental determinants of kidney health. The World Health Organization recommends integrated approaches to improve equity of quality care for people living with long-term conditions, and CKD would be amenable to integrated approaches, however CKD has been neglected from global NCD agendas and there is little data to guide the most effective methods for integrating its care with other long-term conditions (such as hypertension, diabetes and HIV infection), particularly in low-income settings such as Malawi.

The aim of this study is to explore current experiences of care for CKD and related long-term conditions, and to qualitatively evaluate the acceptability and feasibility of different potential approaches to integrating their care, amongst different stakeholders groups in Malawi.

Study Overview

Study Type

Observational

Enrollment (Estimated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Blantyre, Malawi
        • Malawi Liverpool Wellcome Clinical Research Programme
        • Sub-Investigator:
          • Chimota Phiri
        • Contact:
        • Contact:
        • Principal Investigator:
          • Henry Mwandumba
        • Sub-Investigator:
          • Felix Limbani
        • Sub-Investigator:
          • Charlotte Snead

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

- We will recruit adults aged 18 years and older from the following stakeholder groups:

  • Patients
  • Caregivers
  • Healthcare workers (HCWs)
  • Policy makers

Patients will be adults with, or at risk of, CKD and at least one other long-term health condition, who receive outpatient care at Queen Elizabeth Central Hospital (QECH) in Blantyre, Chiradzulu District Hospital or primary health centres within Chiradzulu district.

  • Caregivers of patients from meeting eligibility criteria will also be invited to participate, if they are identified by the patient to be their primary caregiver.
  • Healthcare workers (HCWs) will be recruited from amongst staff working at any of the named study locations, whose role involves caring for patients with CKD and/or other long-term health conditions.
  • Policy makers will be individuals with leading roles in planning, managing and implementing services and policies for non-communicable diseases and/or other long-term conditions in Malawi

Description

Inclusion Criteria:

  • Eligibility criteria for each of the participant groups described above are as follows:

Patients:

  1. Adults aged ≥ 18 years
  2. Diagnosed with CKD, or at risk of CKD, AND at least one other long-term health condition out of:

    • Hypertension
    • Diabetes mellitus
    • HIV infection
    • Heart failure
    • Stroke (See Table 1 for diagnostic inclusion criteria for each of the above conditions)
  3. Receiving outpatient care at one of the selected study sites, for at least 6 months

Caregivers:

  1. Adults aged ≥ 18 years
  2. Identified by a patient meeting the above inclusion criteria to be their primary caregiver

Healthcare workers:

  • Adults aged ≥ 18 years
  • Currently employed as a healthcare worker at either QECH, Chiradzulu District Hospital, Ndunde Health Centre or Namadzi Health Centre.
  • Working in an outpatient clinic environments where care is delivered for patients with any of the above conditions, which may include (but is not limited to) the following:

    • CKD clinic (QECH)
    • Hypertension clinic (QECH)
    • Diabetes clinic (QECH)
    • HIV clinic (all study locations, including the Lighthouse clinic at QECH)
    • Cardiology /chest clinic (QECH)
    • General non-communicable disease (Chiradzulu District Hospital and its referring primary health centres)

Policy makers

  • Adults aged ≥ 18 years
  • Identified through stakeholder mapping and/or snowball sampling to have a leading role relevant to planning, managing and implementing services and/or policies for NCDs and/or other LTCs.

Exclusion Criteria:

  • • Under 18 years of age

    • Acute physical or mental illness, which requires urgent treatment and might impact on ability to participate in and complete interview
    • Current hospital inpatient
    • Unable to participate in interview due to severe communication difficulties (e.g. aphasia), confusion or behavioural disturbance
    • Declines consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients and caregivers
Patients aged 18 years and over with CKD, or at risk of CKD, who have at least one other long-term condition, and who are receiving care at either Queen Elizabeth Central Hospital in Blantyre, Chiradzulu District Hospital, Namadzi or Ndunde primary health care centres. Caregivers will be the caregivers of patients meeting these conditions.
The patient participants are people who are already receiving healthcare for CKD and/or hypertension, diabetes, HIV, heart failure and/or stroke at one of the named study sites, for at least 6 months prior to recruitment into this qualitative study. The caregiver participants are caregivers for patients meeting these criteria.
Healthcare workers
Healthcare workers, aged 18 years and over, providing care for patients with CKD and other long-term health conditions at Queen Elizabeth Central Hospital in Blantyre, Chiradzulu District Hospital, Namadzi or Ndunde primary health care centres.
The healthcare worker participants are all providing care to patients with long-tem conditions, at one of the names study sites
Policy makers
Policy makers with roles in policy making related to CKD and other long-term health conditions in Malawi.
The policy makers recruited to this study will be individuals involved in policy making for long-term conditions in Malawi

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Codes and themes
Time Frame: 6 months from end of data collection
The outcomes of this study will be the codes and themes identified through thematic analysis of the interview and focus group discussion transcripts.
6 months from end of data collection

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

February 17, 2025

Primary Completion (Estimated)

December 31, 2025

Study Completion (Estimated)

March 5, 2026

Study Registration Dates

First Submitted

January 29, 2025

First Submitted That Met QC Criteria

January 29, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 29, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Access may be granted to pseudonymised interview transcripts to approved researchers for the purposes of secondary analyses, only following completion of the analysis and subject to approval by the Malawi Liverpool Wellcome Programme (MLW) research strategy group.

IPD Sharing Time Frame

After completion of the main analysis, and up to a maximum of 5 years after completion fo the study

IPD Sharing Access Criteria

Subject to application to the MLW research strategy group and their approval

IPD Sharing Supporting Information Type

  • ANALYTIC_CODE
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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