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Heart Smart Program for Cardiovascular Disease (Heart Smart Trial)

N/A

Waitlist Available

Led By Stacey E Rosen, MD

Research Sponsored by Northwell Health

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 1 year

Awards & highlights

No Placebo-Only Group

Summary

This trial seeks to improve heart health in women with a 6-week program to help reduce risk factors for heart disease over a year. The program includes weekly didactic sessions and an online discussion group.

Eligible Conditions

Cardiovascular Risk

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 1 year

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~1 year

This trial's timeline: 3 weeks for screening, Varies for treatment, and 1 year for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.

Primary study objectives

Decreased Blood Pressure

Decreased Body Mass Index (BMI)

Decreased Low Density Lipoprotein Cholesterol (LDL-C)

+2 more

Secondary study objectives

Decreased Depression Score

Decreased Psychosocial Stress

Decreased Sleep Disturbance

Awards & Highlights

No Placebo-Only Group

All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups

Experimental Treatment

Group I: Heart Smart Interventional ProgramExperimental Treatment1 Intervention

Subjects participate in this 6-week intervention which include a weekly didactic session, with each week devoted to a different theme (food, exercise, etc). The intervention will follow the program outlined in the book "Heart Smart for Women: Six S. T. E. P. S. in Six Weeks to Heart-Healthy Living."

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