Reducing Cognitive Impairment by Management of Heart Failure as a Modifiable Risk Factor

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBaker Heart and Diabetes Institute

About this trial

This study will test the feasibility and effectiveness of an innovative model of care for cognitively impaired patients with heart failure. This program aims to improve cognition, reduce dementia risk and cardiovascular events, and will be supported by innovative digital technology for wide scale rollout and implementation. Findings from this research will transform the way healthcare is delivered to cognitively impaired patients with heart disease who have a very high risk of developing dementia.

Eligibility criteria

Qualifiers

Hospitalised with HF as primary or secondary diagnosis.

At least mild cognitive impairment (CI) based on Montreal Cognitive Assessment (MoCA) on hospital discharge.

Disqualifiers

Unable to provide written consent; requiring palliative care; or participating in another RCT

Recovery of cognitive function shortly after hospital discharge: to ensure that we only include patients with "true" CI, any patients with a repeated MoCA>25 at 2 weeks post-discharge will be excluded.

Terminal illness (eg. cancer) that may influence 12-month prognosis.

Trial design

Treatments tested in this trial

  • Disease management program

Treatment groups

168 Participants
are divided into 2 treatment groups