RECRUITING

Mind Your Heart-II

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This projects studies the role of mindfulness training (MT) to improve self-care among patients with heart failure and cognitive impairment.

Official Title

Targeting Cognitive Function and Interoceptive Awareness to Improve Self-management in Patients With Co-morbid Heart Failure and Cognitive Impairment.

Quick Facts

Study Start:2022-11-30

Study Completion:2027-06-02

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05431192

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Age \> 18 years old * A documented diagnosis of HF * Access to a telephone * Mild cognitive impairment (MoCA score \< = 26) * Ability to understand and speak English or Spanish	* Unwillingness/inability to provide informed consent * Reversible causes of HF (e.g., takotsubo syndrome; myocarditis) * Severe hearing impairment not allowing phone delivery * Suicidal ideation or plan * Current (at least once a month) mind/body practice * Planning to move out of the area during the study period * Severe cognitive impairment (MoCA scores \< 15) * New York Heart Association (NYHA) class IV heart failure or clinically unstable * Ongoing psychiatric or neurologic conditions * Current enrollment in another study

Inclusion Criteria

Exclusion Criteria

* Age \> 18 years old
* A documented diagnosis of HF
* Access to a telephone
* Mild cognitive impairment (MoCA score \< = 26)
* Ability to understand and speak English or Spanish

* Unwillingness/inability to provide informed consent
* Reversible causes of HF (e.g., takotsubo syndrome; myocarditis)
* Severe hearing impairment not allowing phone delivery
* Suicidal ideation or plan
* Current (at least once a month) mind/body practice
* Planning to move out of the area during the study period
* Severe cognitive impairment (MoCA scores \< 15)
* New York Heart Association (NYHA) class IV heart failure or clinically unstable
* Ongoing psychiatric or neurologic conditions
* Current enrollment in another study

Contacts and Locations

Study Contact

Elena Salmoirago-Blotcher, MD, PhD

CONTACT

401-793-8325

Elena_Salmoirago-Blotcher@brown.edu

Janice Tripolone, MS

CONTACT

JTripolone@lifespan.org

Principal Investigator

Elena Salmoirago-Blotcher, MD, PhD

PRINCIPAL_INVESTIGATOR

Cardiovascular Institute, The Miriam Hospital, Brown University

Study Locations (Sites)

The Miriam Hospital

Providence, Rhode Island, 02906

United States

Collaborators and Investigators

Sponsor: The Miriam Hospital

Elena Salmoirago-Blotcher, MD, PhD, PRINCIPAL_INVESTIGATOR, Cardiovascular Institute, The Miriam Hospital, Brown University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-11-30

Study Completion Date2027-06-02

Study Record Updates

Study Start Date2022-11-30

Study Completion Date2027-06-02

Terms related to this study

Additional Relevant MeSH Terms

Heart Failure
Cognitive Impairment