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Behavioral Intervention

Internet-based Positive Psychological Intervention for Cardiovascular Risk

N/A
Waitlist Available
Led By Rosalba Hernandez, PhD
Research Sponsored by University of Illinois at Urbana-Champaign
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 baseline, 5-, and 12-weeks
Awards & highlights
No Placebo-Only Group

Summary

The largest epidemiologic study of Hispanic/Latino participants thus far, i.e., the Hispanic Community Health Study/Study of Latinos (HCHS/SOL) documented that 80% of men and 71% of women have at least one major cardiovascular disease (CVD) risk factor. The American Heart Association emphasizes that current CVD prevention efforts are sparse and ineffectual in minority populations and acknowledges the need for new and more effective disease prevention strategies. This proof-of-concept study and pilot randomized clinical trial seeks to implement and evaluate a novel internet-based 5-week Positive Psychology (PP) Intervention (compared to an attention control condition) in Hispanic/Latino adults with uncontrolled hypertension, i.e., elevated 24-hour ambulatory blood pressure, with primary interest in testing efficacy for clinically meaningful improvements in cardiovascular function.

Eligible Conditions
  • High blood pressure
  • Cardiovascular Risk

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 5-, and 12-weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 5-, and 12-weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change from Baseline Ambulatory Blood Pressure at 5- and 12-weeks
Secondary study objectives
12-Item Short Form Survey: Change in Self-Reported Mental and Physical Health at 5- and 12-weeks
Mental Depression
General Well-being Schedule: Change in Baseline Emotional Vitality at 5- and 12-weeks
+7 more
Other study objectives
Change in Heart Rate Variability
Body Weight Changes
Diet: Change in Hypertension-related Health Behavior(s)
+1 more

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: Internet-based Positive Psychological InterventionExperimental Treatment1 Intervention
The investigator's culturally-tailored internet-based Positive Psychology (PP) Intervention is a non-pharmacotherapy approach aimed at increasing positive emotional experiences by teaching individuals to engage in intentional activities known to increase psychological and emotional well-being through targeting of constructs such as optimism, gratitude, mindfulness/relaxation, and resilience.
Group II: Attention Control GroupActive Control1 Intervention
Participants will complete computerized surveys to document the frequency of positive and negative emotions experienced in daily life. The attention control group will be given the option to access our positive psychological intervention and associated content via the web at the conclusion of the 12-week data collection phase.

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Who is running the clinical trial?

University of Illinois at Urbana-ChampaignLead Sponsor
197 Previous Clinical Trials
38,205 Total Patients Enrolled
2 Trials studying Cardiovascular Risk
150 Patients Enrolled for Cardiovascular Risk
Rosenfeld Heart Foundation GrantUNKNOWN
Rosalba Hernandez, PhDPrincipal InvestigatorUniversity of Illinois at Urbana-Champaign
1 Previous Clinical Trials
84 Total Patients Enrolled
~11 spots leftby Nov 2025