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Behavioral Intervention
Tough Talks COVID Intervention for Vaccine Uptake
N/A
Waitlist Available
Led By Lisa Hightow-Weidman, MD, MPH
Research Sponsored by Florida State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up month 3
Awards & highlights
No Placebo-Only Group
Summary
This trial tests whether a mobile app called TT-C can help increase COVID-19 vaccination rates among Black young adults in Alabama, Georgia, and North Carolina. The app provides information to boost confidence in vaccines. Participants receive either standard vaccine information or access to the TT-C app.
Who is the study for?
This trial is for African American young adults aged 18-29 who live in Alabama, Georgia, or North Carolina. They must be able to speak and read English, have access to a personal smartphone, and not yet received the full COVID vaccine series.
What is being tested?
The study compares two groups: one receives standard care while the other gets the Tough Talks COVID (TT-C) intervention. The goal is to see if TT-C increases COVID-19 vaccine uptake among participants more effectively than usual methods.
What are the potential side effects?
Since this trial focuses on increasing vaccine uptake through an educational intervention rather than testing a medical product directly, it does not involve typical drug side effects. However, there may be indirect effects related to changes in knowledge or attitudes.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ month 3
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~month 3
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
COVID Vaccine Uptake at Month 1
COVID Vaccine Uptake at Month 3
Secondary study objectives
COVID Vaccine Confidence
COVID Vaccine Hesitancy
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: TT-C InterventionExperimental Treatment1 Intervention
Research staff will provide access to the TT-COVID app for one-month, which will provide knowledge about the COVID-19 vaccine, address mis-information, and include multi-media digital stories from study participant's peers.
Group II: Standard of Care (Control)Active Control1 Intervention
Research staff will provide COVID vaccine materials from the Centers for Disease Control (CDC) to those participants in the Standard of Care (SOC) arm.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Tough Talks COVID
2023
N/A
~360
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for COVID-19 include traditional Chinese medicine (TCM), convalescent plasma (CP), and behavioral interventions. TCM formulations are used to boost the immune system and alleviate symptoms, though their molecular mechanisms are not fully understood.
CP involves transfusing plasma from recovered COVID-19 patients to provide passive immunity through antibodies. Behavioral interventions, like the TT-C trial, aim to increase vaccine uptake by addressing vaccine hesitancy, improving confidence, and enhancing knowledge about vaccines.
This is crucial for COVID-19 patients as higher vaccine uptake can lead to greater community immunity, reducing the spread and severity of the disease.
A bibliometric analysis of research related Chinese Medicine in the prevention and treatment of corona virus disease 2019.How Are Emerging Data Translated Into Clinical Practice? A Mixed Methods Investigation of Coronavirus Disease 2019 Institutional Treatment Protocols.Neurological risks and benefits of cytokine-based treatments in coronavirus disease 2019: from preclinical to clinical evidence.
A bibliometric analysis of research related Chinese Medicine in the prevention and treatment of corona virus disease 2019.How Are Emerging Data Translated Into Clinical Practice? A Mixed Methods Investigation of Coronavirus Disease 2019 Institutional Treatment Protocols.Neurological risks and benefits of cytokine-based treatments in coronavirus disease 2019: from preclinical to clinical evidence.
Find a Location
Who is running the clinical trial?
Florida State UniversityLead Sponsor
220 Previous Clinical Trials
36,095 Total Patients Enrolled
National Institute on Minority Health and Health Disparities (NIMHD)NIH
429 Previous Clinical Trials
1,370,761 Total Patients Enrolled
University of North Carolina, Chapel HillLead Sponsor
1,553 Previous Clinical Trials
4,292,626 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are either younger than 18 or older than 29 years old.You have received all doses of the COVID vaccine, including the booster shot, or have participated in a previous vaccine trial.
Research Study Groups:
This trial has the following groups:- Group 1: TT-C Intervention
- Group 2: Standard of Care (Control)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Coronavirus Patient Testimony for trial: Trial Name: NCT05490329 — N/A
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