HARP Mindfulness Study

Recruiting N/A Interventional Study
Cardiovascular Diseases
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
160 (estimated)
Sponsor
NYU Langone Health · Other
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About This Trial
This study was designed using the Multiphase Optimization Strategy (MOST) framework to determine whether two supplemental components increase the efficacy of a mindfulness-based cognitive therapy program delivered via telephone (MBCT-T) for psychological distress. Specifically, this study will test mindfulness booster sessions to follow a standard 8-week MBCT-T intervention, as well as website sup…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients meeting one of the following criteria: * Has a diagnosis of ischemic heart disease (ICD-10 codes I20 - I25) with no cardiac hospitalizations in the past 6 months * Has cardiovascular disease risk factors without meeting a diagnosis of ischemic heart disease or ha…
Contacts

Tanya Spruill

646-501-3429

Tanya.Spruill@nyulangone.org

CONTACT