MYH-II: Mind Your Heart-II

Sponsor
The Miriam Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05431192
Collaborator
National Institute on Aging (NIA) (NIH)
176
1
2
56
3.1

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Mindfulness Training + Enhanced Usual Care
  • Other: Enhanced Usual Care
N/A

Detailed Description

Stable outpatients patients with co-morbid heart failure (HF) and mild cognitive impairment (MCI) (n=176) will be randomly assigned to phone-delivered MT (a weekly, 30-minute session for 8 weeks integrated with 20-min daily guided individual practice via digital recordings) plus enhanced usual care (EUC) or to EUC alone. Per current recommendations, usual care will be enhanced in both groups with self-care education materials. At baseline, 3 months (end of treatment), and 9 months since baseline participants will undergo comprehensive assessments of cognitive function, psycho-behavioral factors, cardiac vagal control, and HF biomarkers.

This study has the following objectives:
  1. To study the role of MT in improving cognitive function and HF self-care in patients with co-morbid HF and MCI. We hypothesize: 1a) Cognitive function will improve in MT vs. EUC at end of treatment (3 months); 1b) Improvements in cognitive function at end of treatment will mediate effects on self-care and HF biomarkers at follow-up (9 months since baseline).

  2. To study the role of MT in improving interoceptive awareness and HF self-care in patients with co-morbid HF and MCI. We hypothesize: 2a) Interoceptive awareness will improve in MT vs. EUC at 3 months, and 2b) Changes in interoceptive awareness at end of treatment will mediate improvements in self-care and HF biomarkers at 9 months follow-up.

  3. To study the mechanistic pathway linking MT, vagal control and cognitive function. We hypothesize: 3a) Vagal control will improve in MT vs. EUC at end of treatment (3 months); 3b) Changes in vagal control will mediate improvements in cognitive performance at 9 months of follow-up.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
176 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Care Provider, Investigator, Outcomes Assessor)
Masking Description:
Participants will not be masked to intervention allocation. The PI, the co-investigators, and personnel responsible for data management and analysis will be blinded to participants' exposure status. Unblinded personnel will include the PD, the RA, and the MT instructors. Blinding the PD would be impossible given that she will be responsible for randomization and AEs monitoring. The RA will be responsible for data collection and will not be blinded. We note, however, that study participants will independently perform all assessments via computer interface with no RA involvement. The mindfulness instructors will be aware of the allocation status of the participants but will remain masked to the study hypotheses.
Primary Purpose:
Other
Official Title:
Targeting Cognitive Function and Interoceptive Awareness to Improve Self-management in Patients With Co-morbid Heart Failure and Cognitive Impairment.
Anticipated Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Dec 2, 2026
Anticipated Study Completion Date :
Jun 2, 2027

Arms and Interventions

Arm Intervention/Treatment
Experimental: Mindful Training + Enhanced Usual Care

Participants will receive a 30-minute, individual, phone-delivered session once a week for 8 weeks.

Behavioral: Mindfulness Training + Enhanced Usual Care
Participants will receive a 30-minute, individual, phone-delivered session once a week for 8 weeks. MT involves training in the following (1) Awareness of breath; (2) Body scan; (3) Directing attention to simple activities of daily life; (4) Becoming aware of own thoughts and emotions; (5) "Open awareness" - a technique by which the participant is invited to direct his/her attention to any event arising in their field of experience at a given moment. In addition, participants will practice mindfulness techniques for 20 minutes daily on their own with the guidance of a digitally recorded, standardized guided mindfulness practice.

Other: Enhanced Usual Care alone

Usual care.

Other: Enhanced Usual Care
Usual care will be enhanced in BOTH conditions with printed education materials provided to all participants using publicly available materials (the "Healthier Living with Heart Failure" guide available at the AHA Heart Failure Resource Center).66 The guide is organized in 7 chapters containing information on topics such as understanding HF, making healthy lifestyle changes, managing HF symptoms, taking medications, and living well with HF. Printed materials will be mailed weekly to all participants during the first 8 weeks of the study.

Outcome Measures

Primary Outcome Measures

  1. Change in average Fluid Cognition Composite score from the NIH Toolbox Fluid Cognition Battery. [Baseline, 3 months, 9 months]

    The NIH Toolbox is comprised of seven cognitive tests, of which two measure crystallized cognitive ability (i.e., vocabulary and reading) and five tests measure fluid cognitive functioning (i.e., working memory, memory, speed of processing, and executive function). The fluid cognition composite score is obtained by averaging the normalized scores of the Fluid Cognition measures. Higher scores indicate higher levels of functioning. A score ~ 100 indicates average fluid cognitive ability compared with others nationally. Scores ~115 suggest above-average ability, while scores ~130 suggest superior ability. Conversely, a score in the range of 85 suggests below-average ability, and a score ~ 70 or below suggests significant impairment.

Secondary Outcome Measures

  1. Change in average Multidimensional Assessment of Interoceptive Awareness (MAIA) scores. [Baseline, 3 months, 9 months]

    The MAIA is a 32-item, self-report measure composed of eight individual scales, specifically: Noticing; Not Distracting; Not-Worrying; Attention Regulation; Emotional Awareness; Self-Regulation; Body Listening; and Trusting. Items are rated on a 6-point Likert scale (0-5) with '0' indicating 'Never' and '5' indicating 'Always'. Higher scores on each subscale indicate higher levels of interoceptive awareness.There are no standard normal values for each MAIA sub-scale; the range in previous samples from our group for the Not Distracting Score was 1-14. ; MAIA: Not Worrying Score 4-13; MAIA: Attention Regulation Score 4-35; MAIA: Emotional Awareness Score 5-25; MAIA: Self-Regulation Score 4-20; MAIA: Body Listening Score 1-15; MAIA: Trusting Score 3-15.

  2. Change in average Heart Failure (HF) Self-Care total scores. [Baseline, 3 months, 9 months]

    The Self-care of HF Index (SCHFI) v.7.2., is a psychometrically valid, self-report instrument with three separate scales: Self-Care Maintenance (which captures treatment adherence and healthy behaviors), Symptom Perception (which assesses the ability to detect and interpret physical symptoms), and Self-Care Management (the response to symptoms when they occur). Reliability is > 0.70 and scores range from 0 to 100; higher scores indicate better self-care.

  3. Change in average Depression subscale score on the Hospital Anxiety and Depression Scale (HADS). [Baseline, 3 months, 9 months]

    The HADS is a self-reported measure with two sub-scales (scores 0-21) measuring anxiety and depression, with higher scores indicating greater psychological morbidity. A good correlation has been reported between the HADS and other commonly used measures of depression. The HADS has been validated in cardiac patients.

  4. Change in average Kansas City Cardiomyopathy Questionnaire (KCCQ) Health Scores. [Baseline, 3 months, 9 months]

    The Kansas City Cardiomyopathy Questionnaire (KCCQ) quantifies HF-specific physical limitations, symptom frequency, severity and change over time, overall quality of life, social interference, and knowledge. Responses are scored on a Likert scale and summed. Higher scores indicate higher quality of life. Construct validity and sensitivity of the KCCQ have been demonstrated.

  5. Change in high frequency power heart rate variability (hf-HRV) in Ln msec2. [Baseline, 3 months, 9 months]

    High-frequency band is an index of cardiovagal control. High frequency power (hf-HRV) in Ln msec2 , a demonstrated index of vagal activity, will be determined by averaging high frequency values for 10 minute segments at each visit. The proposed methods are based on standards established in the literature.

  6. Change in B-type natriuretic peptide (BNP) levels. [Baseline, 3 months, 9 months]

    BNP is a marker of HF disease severity, elevated filling pressures, clinical outcomes, and is responsive to interventions (e.g., exercise). Specimens are collected in a plastic EDTA tube , centrifuged and separated plasma samples are stored at -20°C until testing. Assays will be analyzed using the ADVIA Centaur BNP assay, a fully automated two-site sandwich immunoassay using direct chemiluminescent technology . The ADVIA Centaur BNP assay measures BNP concentrations up to 5000 pg/mL with a minimum detectable concentration (analytical sensitivity) of < 2.0 pg/mL and shows high specificity for BNP.

  7. Change in average 6-min walk test (6MWT) distance. [Baseline, 3 months, 9 months]

    The 6MWT measures the distance a patient can walk on a level course in 6 min. It is a measure of functional capacity that correlates with peak oxygen uptake and is positively associated with survival in patients with cardiovascular disease. A higher value (in meters) indicates better functional capacity. The 6MWT distance in healthy adults has been reported to range from 400 to 700 meters.

Other Outcome Measures

  1. HF hospital readmissions [9 months]

    Proportion of patients admitted to the hospital with a diagnosis of HF. HF hospital admissions will be tracked via EMR and direct inquiry with participants.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age > 18 years old

  • A documented diagnosis of HF

  • Access to a telephone

  • Ability to understand and speak English or Spanish

Exclusion Criteria:
  • 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 (BOMC79 scores > 10)

  • New York Heart Association61 (NYHA) class IV heart failure or clinically unstable

  • Ongoing psychiatric or neurologic conditions

  • Current enrollment in another study

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Miriam Hospital Providence Rhode Island United States 02906

Sponsors and Collaborators

  • The Miriam Hospital
  • National Institute on Aging (NIA)

Investigators

  • Principal Investigator: Elena Salmoirago-Blotcher, MD, PhD, Cardiovascular Institute, The Miriam Hospital, Brown University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Elena Salmoirago-Blotcher, Senior Research Scientist, The Miriam Hospital
ClinicalTrials.gov Identifier:
NCT05431192
Other Study ID Numbers:
  • R01AG076438
  • R01AG076438
First Posted:
Jun 24, 2022
Last Update Posted:
Aug 24, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2022