Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT05841784

HARP Mindfulness Study

Led by NYU Langone Health · Updated on 2026-04-17

160

Participants Needed

1

Research Sites

85 weeks

Total Duration

On this page

Sponsors

N

NYU Langone Health

Lead Sponsor

A

American Heart Association

Collaborating Sponsor

AI-Summary

What this Trial Is About

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 support in patients with heart disease and/or heart disease risk factors.

CONDITIONS

Official Title

HARP Mindfulness Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults with ischemic heart disease (no cardiac hospitalizations in past 6 months) or with cardiovascular disease risk factors such as hypertension, diabetes, or hyperlipidemia
  • Elevated stress with PSS-10 score 15 or higher
  • Mild to moderate depressive symptoms with PHQ-9 score between 5 and 14
  • Mild or greater anxiety with GAD-7 score 5 or higher
  • Willing to provide informed consent and follow the study protocol
  • Able to read and communicate in English
Not Eligible

You will not qualify if you...

  • Active suicidal thoughts
  • History or current diagnosis of psychosis
  • Significant cognitive impairment noted in medical records or during screening
  • Significant hearing loss
  • Currently participating in another behavioral clinical trial
  • Previously received the MBCT-T intervention in a clinical trial

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

NYU Langone Health

New York, New York, United States, 10016

Actively Recruiting

Loading map...

Research Team

T

Tanya Spruill

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

FACTORIAL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

4

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here