Actively Recruiting

Phase Not Applicable
Age: 18Years - 39Years
All Genders
Healthy Volunteers
ID07623733

Support Your Heart: Feasibility Trial of a Cardiovascular Health Intervention for Young Adults, Phase 1

Led by George Washington University · Updated on 2026-06-03

20

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

Sponsors

G

George Washington University

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating the feasibility and acceptability of the "Support Your Heart" (SYH) study, a phone-based program aimed at improving cardiovascular health in young adults aged 18 to 39. This pilot study focuses on factors like social isolation, loneliness, stress, and lifestyle behaviors that affect heart health, particularly those with at least two risk factors such as insufficient sleep, low physical activity, tobacco use, high body mass index, poor diet, or elevated cholesterol, blood pressure, or HbA1c. Participants receive weekly 20-30 minute phone calls from a SYH health coach over 12 weeks. These calls include reviewing key concepts, personalized progress updates, goal setting, mindfulness, relaxation training, and support to encourage healthier lifestyle changes. The program aims to improve American Heart Association Life's Essential 8 metrics while addressing social and emotional factors. During the study, participants complete baseline surveys and follow-up assessments at 4, 8, and 12 weeks to track progress and satisfaction. Researchers will measure the program's burden, acceptability, adherence, retention, and changes in cardiovascular health metrics. This study may help develop effective phone-based support to reduce cardiovascular risks and improve overall well-being in young adults.

CONDITIONS

Brief Title

Support Your Heart, Phase 1

Who Can Participate

Age: 18Years - 39Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 39 years at enrollment
  • Living in the Washington DC area
  • Having at least two risk factors for cardiovascular disease, such as not enough sleep, insufficient physical activity, tobacco or nicotine product use, elevated body mass index, poor diet, high cholesterol, high blood pressure, or elevated HbA1c
Not Eligible

You will not qualify if you...

  • Major medical condition or chronic disease that limits physical activity or increases risk, including type 1 or type 2 diabetes, recent stroke, very high blood pressure, kidney or lung disease requiring oxygen, recent orthopedic injury, significant surgery in last 6 months, HbA1c over 6.5%, or total cholesterol over 240 mg/dL
  • Planning to become pregnant during the study
  • Psychiatric hospitalization, psychosis, or suicide attempt within the past 12 months
  • Alcohol or substance use disorder
  • Eating disorder
  • Conditions or behaviors that interfere with study participation, such as inability to communicate with staff, unwillingness to accept treatment assignments, or current involvement in another lifestyle intervention study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 in-person screening visit

Outpatient Treatment

Duration - 12 weeks

Participants receive weekly telephone-based health coaching calls to address cardiovascular health and lifestyle behaviors.

Weekly calls lasting 20 to 30 minutes each

Follow-up

Duration - Up to 12 weeks

Participants complete follow-up assessments to measure progress and outcomes after the health coaching intervention.

3 follow-up assessments at 4, 8, and 12 weeks

Trial Site Locations

Total: 1 location

1

GW

Washington D.C., District of Columbia, United States, 20052

Actively Recruiting

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Research Team

M

Melissa Napolitano, PhD

C

Carmen Ortega-Santos, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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