About this trial
The aim of this study is to conduct a mixed methods process evaluation of the META trial. Semi-structured interviews, focus groups, and brief questionnaires will be conducted with a purposive sample of participants (patients and healthcare providers) who were involved in the trial to explore the feasibility, acceptability and perceived effectiveness of the trial intervention.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Participants who participated in the META Trial
Participants who have the capacity to provide written informed consent
Disqualifiers
None
Trial population
All participants that took part in the META trial will be able to participate in this study. Not all participants involved in the META trial will be included in this study. However, participants will be purposefully sampled to be reflective of the population who participated in the META trial.
Trial design
Case-only
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Qualitative interview, focus group, and brief questionnaire findings
The primary outcome will the findings of in-depth semi-structured qualitative interviews, focus groups, and brief questionnaires with a purposive sample of patients and HCPs who participated in the META trial (n=50-60).
Locations
Sponsors and contacts
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University College Dublin
Lead sponsor
University College London Institute for Global Health
Collaborator
National Institute for Medical Research, Tanzania
Collaborator
Shree Hindu Mandal Hospital, Tanzania
Collaborator
Barcelona Institute for Global Health
Collaborator
This trial is not recruiting at the moment. You can still explore other options: