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Intervention Arm for High Blood Pressure
N/A
Waitlist Available
Research Sponsored by Rutgers, The State University of New Jersey
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, at end of 6-week intervention, and 1 month post-6-week intervention
Awards & highlights
Summary
This trial will test a youth-led hypertension education digital badge to see if it can help adults with uncontrolled hypertension achieve better blood pressure control.
Eligible Conditions
- High Blood Pressure
- Adolescent Behaviors
- Health Literacy
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, at end of 6-week intervention, and 1 month post-6-week intervention
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, at end of 6-week intervention, and 1 month post-6-week intervention
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
For ED cohort: Blood pressure change
Secondary outcome measures
Both ED cohort: Youth self-efficacy
ED cohort: Adult blood pressure self-care
ED cohort: Adult self-efficacy to manage HTN
+5 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Intervention ArmExperimental Treatment1 Intervention
The intervention is a youth-led HTN education digital intervention, which will be comprised of a 6-week playlist of one module per week comprising the playlist. Youth will learn from the module and will teach the adult in their dyad about hypertension education in each week's themed module.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Youth-Led Hypertension Education Digital Intervention
2021
N/A
~100
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Who is running the clinical trial?
National Center for Advancing Translational Sciences (NCATS)NIH
329 Previous Clinical Trials
402,054 Total Patients Enrolled
Rutgers, The State University of New JerseyLead Sponsor
435 Previous Clinical Trials
64,923 Total Patients Enrolled
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