Scale Development for Organizational Trustworthiness
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Questionnaire.
- Who it may be relevant to
- Registry conditions: Psychometric. Basic parameters: 18 years — 99 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Teaming Researchers Up With Stakeholders to Test Trustworthy Engagement and Measures
Overview
The Teaming Researchers Up with Stakeholders to Test Trustworthy Engagement and Measure (TRUST TEAM) project seeks to better understand the role of organizational trustworthiness in the context of community-engaged research. At its core, how does organizational trustworthiness shape patients and other key stakeholders' involvement in community-academic research collaborations? What characteristics make an organization trustworthy and how does that strengthen relationships between academic organizations and community collaborators? This project is creating a first-of-its-kind psychometrically sound measure of organizational trustworthiness.
Interventions
- Other Questionnaire
This is not an intervention study.
Primary outcome measures
- Development of Organizational Trustworthiness Measure [Time frame: April 2025 to October 2026]
Eligibility criteria
Inclusion criteria
- Community/Advocacy Leaders, Clinician Non-Researchers, Patient Stakeholders
Exclusion criteria
- Clinical Researchers
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07358559 · STUDY25090191