Primary Health Care Delivery Models in Conflict Settings of Cameroon and Nigeria

May 16, 2022 updated by: Lundi-Anne Omam Ngo Bibaa, University of Cambridge

Primary Health Care Landscape in Conflict Settings and Choices of Delivery Models in North West and South West Regions of Cameroon and North East Nigeria

The overall objective of this research is to understand the PHC landscape in conflict-affected settings including choice of PHC delivery models and quality interventions used by humanitarian organisations

Study Overview

Detailed Description

There is sparse evidence to guide the selection and design of primary health care (PHC) services that improves and maintains quality care in humanitarian settings. The Northwest and Southwest regions of Cameroon, and Northeast Nigeria have protracted humanitarian crises. Various models of PHC are used in these settings; ensuring quality of PHC models of care is essential to improve health outcomes. We aim to explore how PHC models are selected by humanitarian organizations and through stakeholder engagement design a toolkit for evaluation of quality in PHC care delivery across different models.

The specific objectives of the study are;

  1. To map different primary health care delivery models used by public, private and humanitarian organization in the conflict affected settings of NWSW Cameroon and North East Nigeria by conducting a mapping survey
  2. To explore the factors influencing the selection of primary health care delivery models used by humanitarian organizations to guide the selection of models of care and strengthening of programming efforts in conflict settings by conducting an exploratory qualitative study
  3. To determine the coverage and gaps in services across the different PHC models to develop a pilot questionnaire to evaluate quality in conflict settings by conducting an exploratory qualitative study

The humanitarian crisis in North West and South West regions of Cameroon and North East Nigeria, has led to the closure of 269/933 and 617/2367 health facilities respectively with over 2.21 million IDPs and 350,000 returnees(2, 3), creating a huge gap in the availability and accessibility of health services to affected communities. The need to conduct this study becomes even more pertinent to inform program developers and donors on key considerations to make before using different models of care, and how quality can be improved to foster sustainability

Study Type

Observational

Enrollment (Anticipated)

200

Contacts and Locations

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

Study Contact

  • Name: LUNDI-ANNE OMAM N BIBAA
  • Phone Number: 0047849529803
  • Email: laon2@cam.ac.uk

Study Contact Backup

Study Locations

    • South West Region
      • Buea, South West Region, Cameroon, 88
        • Recruiting
        • Reach Out Cameroon
        • Contact:
          • Esther Njomo
      • Maiduguri, Nigeria
        • Recruiting
        • Herwa Cdi
        • Contact:
          • Mohammed Ngubdo Hassan
      • Cambridge, United Kingdom, CB39AL
        • Not yet recruiting
        • Lundi-Anne Omam Ngo Bibaa
        • Contact:
          • LUNDI-ANNE OMAM N BIBAA
          • Phone Number: 0047849529803
          • Email: laon2@cam.ac.uk
        • Principal Investigator:
          • Nicholas Tendongfor, PhD
        • Sub-Investigator:
          • Zara Wudiri, MD
        • Sub-Investigator:
          • Esther Njomo Omam, MA
        • Sub-Investigator:
          • Mohammed Ngubdo Hassan, MA

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

21 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

The Study population will be adults of age 21 years and above. The research will be undertaken with staff of humanitarian organizations and internally displaced populations. Project managers, project supervisors, grant writers and frontline workers of humanitarian organizations (UN agencies, international NGOs, national NGOs and CBOs) will be interviewed. Internally displaced persons in urban, peri-urban, rural and hard-to-reach areas. We will purposefully select participants from across the geographical area to ensure wide coverage of experiences/ views. In Cameroon and Nigeria, regions and states will be divided between rural, peri-urban and urban, and humanitarian organisations implementing programs in these areas will be group into urban, peri-urban and rural responders.

Description

Inclusion Criteria:

  • Male and female staff of humanitarian organisations, internally displaced persons (confirmed to be a resident of an IDP or host community);
  • Age 21 years of age or older;
  • Ability to provide informed consent or assent to participate in the research

Exclusion Criteria:

  • Individuals who are mentally ill or with limitations to communicate well;
  • Those who cannot speak or understand the local languages so that they cannot understand the interviewer.
  • Those who refuse to provide consent to the study or who do not want to participate in the study

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

  • Observational Models: Other
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Humanitarian workers
Staff working in humanitarian organisations will be recruited for interviews
The intervention to be evaluated in this study is program design and selection considerations by humanitarian organisations. It will comprise of factors that motivate organisations to chose certain delivery models in providing health care in conflict-affected settings
Internally displaced persons
Internally displaced persons living in conflict settings will be recruited for interviews
The intervention to be evaluated in this study is program design and selection considerations by humanitarian organisations. It will comprise of factors that motivate organisations to chose certain delivery models in providing health care in conflict-affected settings

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of frameworks developed
Time Frame: 12 months
Framework to guide humanitarian organizations in the selection of primary health care models will be collaboratively developed following the results from the study and stakeholders meeting
12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of quality oversight toolkit developed
Time Frame: 12 months
Following the development of a framework to inform the selection of models of care, an "oversight toolkit" for selecting models of care and monitoring a pragmatic set of quality interventions (QI) will be developed. The toolkit will include a composite score drawing from scores across all domains. This will be used to give an overall assessment score of quality.
12 months

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Rosalind Parkes-Ratanshi, University of Cambridge

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 (Actual)

March 17, 2022

Primary Completion (Anticipated)

March 30, 2023

Study Completion (Anticipated)

September 30, 2023

Study Registration Dates

First Submitted

February 17, 2022

First Submitted That Met QC Criteria

March 9, 2022

First Posted (Actual)

March 15, 2022

Study Record Updates

Last Update Posted (Actual)

May 18, 2022

Last Update Submitted That Met QC Criteria

May 16, 2022

Last Verified

May 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • Cambridge

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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