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Theoretically Informed Behavioral Intervention

Theoretically Informed Behavioral Intervention to Prevent HIV-related Comorbidities

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06580184
Enrollment
164
Registered
2024-08-30
Start date
2026-10-01
Completion date
2029-03-31
Last updated
2026-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CVD, HIV, Metabolic Disease

Keywords

Syndemic, HIV, CVD, HTN, Diabetes Mellitus, Cancer, Virtual Reality, Prevention

Brief summary

The goal of this waitlist control clinical trial is to learn if the tailored LEARN 2 platform can prevent HIV-related comorbidities with shared risk factors in men ages 18 and older living with HIV. The main question\[s\] are: 1. Can the virtual environment improve quality of life among these participants? 2. Does the LEARN 2 platform effectively serve as prevention education for HIV comorbidity shared risk factors? Researchers will compare participants receiving the LEARN2 virtual environment intervention to those in a waitlist control group to see if the intervention leads to improvements in quality of life and reductions in risk factors. Participants will be asked to: 1. Engage with the virtual environment weekly. 2. Participate in virtual live health educator sessions. 3. Complete daily assessments of personal health behaviors through Ecological Momentary Assessment.

Detailed description

The goal of this waitlist control clinical trial is to determine the efficacy of the tailored LEARN 2 platform in preventing HIV-related comorbidities characterized by shared risk factors. The principal questions this study aims to address are: 1. Can engagement with the virtual environment enhance the quality of life for participants? 2. Is the LEARN 2 platform effective in providing prevention education of shared risk factors associated with HIV comorbidities? To evaluate these objectives, the investigators will conduct comparisons between participants allocated to the LEARN 2 virtual environment intervention and those assigned to a waitlist control group. This design will facilitate the assessment of whether participation in the LEARN 2 intervention correlates with significant improvements in quality of life metrics (behavioral and psychosocial) and a reduction in associated health risk factors. Participants will be instructed to: 1. Engage with the virtual environment on a weekly basis, exploring tailored health content designed to address their specific needs. 2. Attend virtual live sessions with health educators, where they will receive real-time education on health issues relevant to their condition and associated lifestyle factors using the American Heart Association's Life's Essential 8 as a behavioral prevention framework. 3. Complete daily assessments of their personal health behaviors using Ecological Momentary Assessment (EMA), capturing real-time data on behavioral trends that may influence their health outcomes. This systematic approach aims to generate comprehensive data on the impact of the LEARN 2 intervention on both quality of life and the modulation of health-related behaviors among these at-risk populations.

Interventions

BEHAVIORALLEARN 2 Platform

The LEARN 2 Platform will provide tailored prevention education of HIV-comorbidities with shared risk factors. Participants will navigate LEARN 2 and access targeted health content.

Sponsors

Yale University
Lead SponsorOTHER
National Institute on Minority Health and Health Disparities (NIMHD)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Self-identify as: * living with HIV * English speaking * Access to a device compatible with LEARN 2

Exclusion criteria

\- medical history of serious complications such as heart attack, stroke, cognitive impairment, or cancer.

Design outcomes

Primary

MeasureTime frameDescription
Quality of Life scaleBaseline, 3 and 6 months29-item scale from the PROMIS® Profile 29 for adults. The quality- of-life questions include physical function, anxiety, depression, fatigue, sleep disturbance, ability to participate in social roles and activities, and pain intensity over the past 7 days. Each question, except for the pain intensity question, is measured on a 5-point scale.

Secondary

MeasureTime frameDescription
DietMonths 1, 3, and 51-item that has participants rate how healthy one's eating was that day and has been validated in EMA studies
Physical ActivityMonths 1, 3, and 53 items that assess the number of minutes of light, moderate, and heavy physical activity and has been validated in EMA studies.
Sleep QualityMonths 1, 3, and 51-item that assesses the quality of sleep for the previous night from 1(poor) to 8(extremely rested) and has been validated in EMA
Health Care UtilizationMonths 1, 3, and 5assesses perceived health needs, whether they have a plan to deal with those needs, and whether they saw a health care provider about those needs
Physical Relationship HealthMonths 1, 3, and 54-items that assess whether participants were intimate and type of activity
SmokingMonths 1, 3, and 52-items used in EMA studies that assessed whether the participant smoked and how many cigarettes
Social SupportMonths 1, 3, and 53-item scale that assesses the among of emotional, informational, and tangible support received from their social network
CopingMonths 1, 3, and 57-item scale where participants rate whether they used 7 different coping strategies which has been validated in EMA studies.
Social CohesionMonths 1, 3, and 57-item scale that measures decree of cohesion within a person's neighborhood or community.

Countries

United States

Contacts

CONTACTPenelope Schlesinger
ysn.thelearn2study@yale.edu203 764-7573
PRINCIPAL_INVESTIGATORS. Raquel Ramos, PhD, MBA, MSN

Yale University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 17, 2026