- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07358559
Scale Development for Organizational Trustworthiness (TRUST TEAM)
Teaming Researchers Up With Stakeholders to Test Trustworthy Engagement and Measures
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.
Study Overview
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Virginia A Brown, PhD, MA
- Phone Number: 236 845-424-4040
- Email: brownv@thehastingscenter.org
Study Contact Backup
- Name: Phillip W Schnarrs, PhD
- Phone Number: 512-831-1200
- Email: pws21@pitt.edu
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Community/Advocacy Leaders, Clinician Non-Researchers, Patient Stakeholders
Exclusion Criteria:
- Clinical Researchers
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Development of Organizational Trustworthiness Measure
Time Frame: April 2025 to October 2026
|
Develop and test a measure of organizational trustworthiness
|
April 2025 to October 2026
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Virginia A Brown, PhD, MA, The Hastings Center for Bioethics
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY25090191
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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