Mindfulness may boost Self-Care in heart failure patients with cognitive decline
NCT ID NCT05431192
First seen Jun 24, 2026 · Last updated Aug 06, 2026 · Updated 5 times
Summary
This study tests whether 8 weeks of phone-based mindfulness training can improve self-care and thinking skills in 176 adults with heart failure and mild cognitive impairment. Participants practice techniques like breath awareness and body scanning for 20 minutes daily. The goal is to see if this helps them manage their condition better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- mindfulness training
- What this could lead to
- If it works, this could offer a simple, phone-based way to help people with heart failure and memory problems manage their health better.
- What could go wrong
- This is an early-stage study with only 176 participants. The benefits may be small or not last long, and results may not apply to everyone with heart failure.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 176 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2022
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion 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 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 (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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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The Miriam Hospital
Providence, Rhode Island, 02906, United States
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Other studies related to the condition(s) this trial covers.
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