Conversations You Want About Corona Virus Disease (COVID-19) (COVID-19)

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

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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