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CTC Intervention for High Blood Pressure
N/A
Waitlist Available
Led By Sarah L Cutrona, MD
Research Sponsored by VA Office of Research and Development
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6-months after intervention
Awards & highlights
Study Summary
This trial is designed to see if improving hypertension self-management and lowering blood pressure (BP) in African-American Veterans is possible by having them watch videos and then receive text messages related to the content of the videos.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6-months after intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6-months after intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
BP Measurement Change at Follow-up
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: CTCExperimental Treatment1 Intervention
An integrated peer narrative-based intervention (VIEW > SELECT > GET), beginning with VIEW In-person viewing of VA Stories narratives, followed by SELECT a favorite Veteran] Storyteller, and then GET favorite Storyteller "narrative-aligned" text messages over 6 months
Group II: ControlActive Control1 Intervention
6-month HTN management assessment text messages without narrative component
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
CTC Intervention
2020
N/A
~600
Find a Location
Who is running the clinical trial?
VA Office of Research and DevelopmentLead Sponsor
1,609 Previous Clinical Trials
3,306,003 Total Patients Enrolled
Sarah L Cutrona, MDPrincipal InvestigatorVA Bedford HealthCare System, Bedford, MA
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- This trial is not currently accepting individuals who identify as African American or Black.If you have already participated in our previous VA Stories study as a veteran, you cannot participate again.
Research Study Groups:
This trial has the following groups:- Group 1: CTC
- Group 2: 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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
How many participants are being included in the research program?
"Affirmative. According to clinicaltrials.gov, this investigation is actively accepting participants. The study was first published on November 30th 2020 and has been restlessly revised since then; 600 people are needed across two experiment sites."
Answered by AI
Is there capacity within this trial for additional participants?
"This medical trial, first posted on November 30th 2020 and last updated April 7th 2022 is currently enrolling patients, as indicated by the clinicaltrials.gov listing."
Answered by AI
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