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Challenges and opportunities in clinical field research projects

Challenges and opportunities in clinical field research projects within the Fiocruz Vice-Presidency of Biological Collections and Research clinical research platform

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
REBEC
Registry ID
RBR-75vszpf
Enrollment
50
Registered
2026-05-19
Start date
2025-07-23
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schistosomiasis, Chagas disease, Tuberculosis Public health

Interventions

This is an observational and descriptive mixed-methods field clinical research study with no control group, in which the single participant group will consist of fifty-one participants, including rese

Sponsors

Vice-Presidência de Pesquisa e Coleções Biológicas - VPPCB
Lead Sponsor
Vice-Presidência de Pesquisa e Coleções Biológicas - VPPCB
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age equal to or greater than eighteen years; participants of both sexes; professionals acting as researchers or other members of the teams involved in at least one of the clinical field research projects belonging to the portfolio of the Clinical Research Platform developed between the years two thousand and twenty and two thousand and twenty-three

Exclusion criteria

Exclusion criteria: Researchers and other team members who have less than twelve months of experience in the aforementioned clinical field research projects

Design outcomes

Primary

MeasureTime frame
It is expected that a detailed analysis of strengths, weaknesses, opportunities, and threats will be conducted for the clinical field research projects, verified through the categorization of questionnaire responses into these four strategic dimensions, to support the development of institutional strategies

Secondary

MeasureTime frame
It is expected that a proposal for a Work Instruction for the collection and management of adverse events will be developed, along with a Risk Management Plan model adapted to the reality of clinical field research, as verified by the integration of qualitative data and weaknesses identified during the analysis

Countries

BR

Contacts

Public ContactRenata Diniz

Fundação Oswaldo Cruz

renata.diniz@fiocruz.br+55(21)2598-4242

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Jun 11, 2026