- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05191420
Conversations You Want About Corona Virus Disease (COVID-19) (COVID-19)
May 27, 2026 updated by: Wake Forest University Health Sciences
BECAUSE YOU MATTER: Conversations You Want About COVID-19
Web-enabled virtual topical guide: develop virtual conversations for each concern and intensity level
Study Overview
Status
Terminated
Conditions
Detailed Description
Study will pilot test the virtual topical discussion guide with diverse health care professions and community members to confirm it is clear, relevant, understandable, and culturally appropriate
Study Type
Observational
Enrollment (Actual)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
North Carolina
-
Winston-Salem, North Carolina, United States, 27157
- Wake Forest Health Sciences
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Diverse health care professions and community members
Description
Inclusion Criteria:
- greater than or equal to 18 years of age
- English or Spanish speaking only
Exclusion Criteria:
- less than 18 years of age
- not English or Spanish speaking
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
|
Virtual topical discussion guide
Study will pilot test this virtual topical discussion guide to assess feasibility and acceptability by diverse patient populations.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Time spent with the guide
Time Frame: Week 4
|
Time spent with the guide
|
Week 4
|
|
Number of clinics viewed in the guide
Time Frame: Week 4
|
Number of clinics viewed in the guide
|
Week 4
|
|
Number of content areas accessed
Time Frame: Week 4
|
Number of content areas accessed
|
Week 4
|
|
Time spent with each content area
Time Frame: Week 4
|
Time spent with each content area
|
Week 4
|
|
Helpfulness of Tool
Time Frame: Week 4
|
How helpful was this tool in your decision-making, ranging from 1 not at all helpful to 5 incredibly helpful
|
Week 4
|
|
Number of Subjects saving responses
Time Frame: Week 4
|
Individuals will have the ability to send their guide responses to themselves for later use
|
Week 4
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Katherine A Poehling, MD, Wake Forest Health Sciences
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 9, 2022
Primary Completion (Actual)
May 15, 2023
Study Completion (Actual)
May 15, 2023
Study Registration Dates
First Submitted
January 11, 2022
First Submitted That Met QC Criteria
January 11, 2022
First Posted (Actual)
January 13, 2022
Study Record Updates
Last Update Posted (Actual)
June 1, 2026
Last Update Submitted That Met QC Criteria
May 27, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB00075790
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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