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Understanding the Health Systems and Policy Contexts of Medical Oxygen in Africa and Asia (MOXY-HSP)
Led by Murdoch Childrens Research Institute · Updated on 2026-02-06
1
Participants Needed
6
Research Sites
N/A
Total Duration
On this page
Sponsors
M
Murdoch Childrens Research Institute
Lead Sponsor
U
University of Ibadan
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to understand how national medical oxygen strategies work and achieve impact at both national and local levels across different countries. It focuses on health systems and policy contexts in six countries involved in the Medical Oxygen Implementation program. The study seeks to involve policymakers, implementers, and medical oxygen users to identify challenges and find potential solutions to improve access to medical oxygen. Researchers also aim to generate new data and draw lessons that can inform national and global policy and practice. The study uses a mixed-methods design with three embedded parts: stakeholder analysis, policy-implementation gap analysis, and comparative country case studies. It involves interviews with key informants from government, NGOs, professional associations, private sector, and civil society. The study is conducted in six countries and will be adapted to each context through ongoing collaboration with stakeholders. The research will run for four years and includes annual meetings to refine study topics and methods. Participants will take part in in-depth interviews focusing on national medical oxygen strategies over the four-year study period. Researchers will review policies, analyze program data, and compare findings across countries. The study will monitor how strategies are translated into action and their effects on oxygen service coverage. This involves collecting qualitative and quantitative data to better understand the implementation and challenges of medical oxygen programs within different health systems.
CONDITIONS
Brief Title
Health Systems and Policy Contexts of Medical Oxygen
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years and older
- Key informants representing government, non-governmental agencies, professional associations, private sector, or civil society
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or virtual)
Duration - Up to 4 years
Participants engage in in-depth interviews and provide insights on national medical oxygen strategies across multiple countries.
Repeated interviews over the study period
Duration - Up to 4 years
Participants may take part in national dialogues to review and validate preliminary findings and discuss feasible solutions for medical oxygen policies and practices.
Periodic meetings depending on country context
Trial Site Locations
Total: 6 locations
1
Cambodia
Phnom Penh, Cambodia
Actively Recruiting
2
Lao PDR
Vientiane, Laos
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3
Liberia
Monrovia, Liberia
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4
Nigeria
Ibadan, Nigeria
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5
Rwanda
Kigali, Rwanda
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6
Uganda
Kampala, Uganda
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Research Team
R
Rami Subhi, MBBS, FRACS, MD (Res)
H
Hamish Graham, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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