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Heart FailureHeartMappNCT03827954

HeartMapp: Assessment and Treatment for Heart Failure

A study testing HeartMapp+CT in people with Heart Failure and Cognitive Impairment, run by Posit Science Corporation at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

In the current application, the investigators propose to elaborate upon, reconstruct and advance to pivotal trial readiness a recently validated mobile application (HeartMapp), designed for the ecological momentary assessment and treatment of individuals with Heart Failure (HF). Read more about this study

Who is it for?
Ages 40 years and older
Conditions the study is for
Heart Failure, Cognitive Impairment
What is being tested?
HeartMapp+CT
Could I receive a placebo?
No, everyone receives an active treatment
How many people
28 participants
Where
1 siteUnited States
Study dates
5 Jun 2019to 24 May 2021
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Selection of participants is based on their condition HF and is not based on gender or ethnic considerations, although these are expected to reflect the diverse population of the United States; ethnic minorities will be included when available and recruiting efforts will target a balanced enrollment.
  • Age 40 years or above,
  • Clinical diagnosis of HF as defined by the International Classification of Diseases (ICD-10 codes) and recent hospitalization for HF,
  • New York Heart Association (NYHA) classification II-III,
  • Ability to speak, understand and read English,
  • Adequate hearing, as determined by response to a pure-tone stimulus at 70 decibels or better for 1 \& 2 kHz in each ear, measured using the Welch-Allyn.
  • Intact vision (visual acuity of 20/50 or better, as assessed by a Snellen chart per standard procedure).

Who cannot join

  • Participants meeting any of the following exclusion criteria at baseline will be excluded from study participation.
  • Listed for heart transplant as status 1A,
  • Enrolled in a palliative or hospice care program,
  • Currently enrolled in another research study,
  • Concurrent or previous participation in a cognitive training study within a month of the consent date,
  • Self-reported vision, hearing, or motor difficulties that would interfere with the ability to complete the study interventions,
Show all 14Show fewer
  • Self-reported diagnosis of dementia, stroke, traumatic brain injury, brain tumor, or a neurological disorder that affects cognition or would interfere with the ability to benefit from the study intervention (e.g., Parkinson disease, multiple sclerosis), or any other unstable medical conditions that is predisposing to imminent cognitive or functional decline (e.g., undergoing chemotherapy or radiation),
  • Presence of disability (e.g., aphasia) that may prevent them from completing study related activities,
  • Severe depressive symptoms screened using PHQ-9 with score ≥16,
  • History or current diagnosis of organic mental disorder, schizophrenia, schizoaffective disorder, delusion disorder, psychotic disorder, bipolar disorder, and/or mood congruent or mood incongruent psychotic features or disorders,
  • Evidence of dementia with a score of <20 in the Montreal Cognitive Assessment, (MoCA),
  • Shows signs of intoxication due to current substance abuse (including alcohol and/or illegal drugs),
  • Suicidal thoughts or ideations, or suicide-related behaviors using Columbia-Suicide Severity Rating Scale with 2 months of consent date.
  • Participants who are excluded due to depression, suicidal thoughts or ideation and/or dementia, poor vision or hearing will be referred to the appropriate professionals for thorough evaluation and treatment.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • University of South Florida

    Tampa, Florida, 33559

Other trials in United States

About this study

Official title: HeartMapp: A Closed-loop Assessment and Treatment Mobile Application for Heart Failure. A Pilot Clinical Trial

In the current application, the investigators propose to elaborate upon, reconstruct and advance to pivotal trial readiness a recently validated mobile application (HeartMapp), designed for the ecological momentary assessment and treatment of individuals with Heart Failure (HF). Presently, HeartMapp includes physiological modules (PM) that support self-monitoring and exercises that promote heart health, and cognitive modules (CM) that track and enhance cognitive functions. During the first three-months, the investigators will finalize the cognitive training modules within HeartMapp and release through the quality management system. At the completion of software development, the investigators propose to test the relevant usage and progression variables of the algorithm that will be used to direct engagement with the app.

The investigators will conduct a single arm, open label, pilot clinical trial to examine feasibility and initial efficacy of the HeartMapp+CT (HeartMapp and computerized plasticity-based adaptive cognitive training). The term "CT" refers to computerized training. The study will enroll 32 adults aged 40 and older with a diagnosis of HF and over sample by 25% to reduce attrition for a total of 24 participants enrolled at the end. Participants will complete follow-up assessments at 3- and 6-months after enrollment.

Read the detailed description

Heart failure (HF) is a progressive disease that affects 6.5 million Americans and is projected to reach 10 million by 2020. Presently, treatments for HF are largely comprised of drug therapies targeting pathophysiology and self-administered therapies that require patients to learn, accurately recall and routinely execute complex self-care practices. HF patients are expected to monitor their weight, diet and manage their medications, and are also required to recognize, monitor and report HF related symptoms. However, adopting self-care behaviors are often challenging for patients due to concomitant cognitive impairments, as shown in 30% to 80% of HF patients; a condition which is often complicated by insufficient social support. Multiple studies have shown a direct relationship between cognitive deficits and difficulty with self-care. Thus, there is currently an urgent unmet need for novel patient-centered interventions that are easy to use by older adults with HF that suffer cognitive difficulties and lack social support.

In the current application, investigators propose to elaborate upon, reconstruct and advance to pivotal trial readiness a recently validated mobile application (HeartMapp), designed for the ecological momentary assessment and treatment of individuals with HF. Presently, HeartMapp includes physiological modules (PM) that support self-monitoring and exercises that promote heart health, and cognitive modules (CM) that train participants to enhance cognitive functions. The Posit Science Corporation team of developer and neuroscientists will closely collaborate with investigators at University of South Florida (Drs. Athilingam and Labrador), inventors of the initial version of HeartMapp, to include a clinician-facing dashboard and reporting utility comprised of both PM and CM performance and progress tracking metrics. This Point-of-Care (POC) device will also aid clinical studies of cardiovascular, lung, and blood diseases and disorders by providing continuous monitoring data collected remotely to serve as an open channel between patients and clinicians. A recent usability study of the HeartMapp PM conducted by co-investigator Dr. Athilingam in 25 HF patients was successful; patients found the app easy to use, helpful and engaging. A concurrent pilot clinical trial that examined only CM in 17 HF patients demonstrated that CM improved memory, cognitive speed of processing, and showed trends for improved everyday function and HF self-care. Across all functional outcomes measured, the CM group showed better function post-training relative to controls. Similarly, in our prior research, and in the successful development of related products at Posit Science that demonstrated a core ability to develop multimodal (i.e., assessment and treatment) applications with compelling user experiences that drive strong performance improvements across multiple performance domains.

The investigators will conduct a single arm, open label, pilot clinical trial to examine feasibility and initial efficacy of the HeartMapp+CT (HeartMapp and computerized plasticity-based adaptive cognitive training). The study will enroll 32 adults aged 40 and older with a diagnosis of HF and over sample by 25% to reduce attrition for a total of 24 participants. Participants will complete follow-up assessments at 3- and 6-months after enrollment.

  • The primary outcome is to test the feasibility and initial efficacy of using HeartMapp with computerized plasticity-based adaptive cognitive training (HeartMapp+CT), which will be quantified by measuring app usage and engagement with the apps. Engagement with cognitive training will be calculated as percentage of participants who complete 30 sessions of assigned cognitive training included in HeartMapp. App usability and engagement will be assessed by App access by participants; Accessing App components at least 80% of the days (72 days out of 90-days) will be used to determine app engagement.
  • The secondary outcomes are improvement in cognitive function and HF self-care. If an effect sizes on Cohen's d of d=0.25 or greater relative to controls for these outcomes, HeartMapp will be considered potentially efficacious.
  • Exploratory outcomes include improvement in quality of life, global health, medication adherence, heart rate variability and hospital admission. The investigators will calculate effect sizes using Cohen's d on these outcomes to inform future studies.
Being tested
HeartMapp+CT
Keywords
Heart failure, cognitive impairment, HeartMapp Mobile app, Self-care
Medical subject headings
Heart Failure, Cognitive Dysfunction

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • HeartMapp+CTOther

    HeartMapp+CT is a mobile system that includes physiological modules that support self-monitoring and exercises that promote heart health, and computerized plasticity-based adaptive cognitive training modules that train participants to enhance cognitive functions and ultimately heart failure outcomes.

Study groups in NCT03827954
Study groupRoleWhat they receive
Experimental TreatmentExperimentalHeartMapp+CT
Receives: Other: HeartMapp+CT

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Primary outcome (Feasibility of HeartMapp+CT app usage)

    Above 80% usage of HeartMapp+CT will indicate feasibility of using the app.

    Measured: 3-months

Secondary outcomes (6)
  1. Cognitive outcomes (NIH-Examiner and Neuro QOL questionnaire)

    Cognitive function will be measured using NIH-Examiner and Neuro QOL questionnaire provides a practical opportunity for multidimensional assessment in neurologic and cognitive assessment in clinical research or practice will be used. The internal consistency for this measure is (Cronbach alpha) of the 13 short forms ranged from 0.85 to 0.97. Higher scores on the cognitive measures will indicate improved cognition.

    Measured: up to 6-months (baseline and improvement at 3, and 6 months)

  2. Heart failure Self-care (Self-Care of Heart Failure Index)

    Heart failure self-care will be assessed using the Self-Care of Heart Failure Index Cronbach's alpha of 0.81. The questionnaire measures three domains of self-care: Self-Care Maintenance, Self-management, and Self-Confidence. The questionnaire includes 15-items for a total score of 100. Lower scores indicates better self-care.

    Measured: Up to 6-months (baseline and improvement at 3, and 6 months)

  3. Quality of life related to Heart Failure (Kansas City Cardiomyopathy Questionnaire)

    Quality of life will be measured using Kansas City Cardiomyopathy Questionnaire that include five clinically relevant domains: physical limitations, HF symptom (frequency, severity, and change over time), quality of life, social interference, and self-efficacy. (Cronbach's alpha of 0.66-0.95) higher composite scores indicate better quality of life.

    Measured: Up to 6-months (baseline and improvement at 3, and 6 months)

  4. Physical and Mental Health (PROMISE short-form scale)

    Global physical and mental health will be measured using the PROMISE short-form scale that measures (4 items on overall physical health, physical function, pain, and fatigue) and global mental health (4 items on quality of life, mental health, satisfaction with social activities, and emotional problems) with internal consistency .81-.86, respectively. Lower score of both domains indicates better physical and mental health.

    Measured: Up to 6-months (baseline and improvement at and 6 months)

  5. Clinical outcomes (6-minute Walk Test)

    Physical capacity will be measured by distance walked using 6-minute Walk Test

    Measured: Up to 6-months (baseline and improvement at 3, and 6 months)

  6. Heart rate Variability

    Heart rate variability measured using BioPatch to determine improvement overtime

    Measured: Up to 6-months (baseline and improvement at 3, and 6 months)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Feb 2019
  2. Study start5 Jun 2019
  3. Primary completion24 May 2021
  4. Study completion24 May 2021

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Model description
A single arm, open label, pilot clinical trial to examine feasibility and initial efficacy of the HeartMapp+CT (HeartMapp and computerized plasticity-based adaptive cognitive training).
Masking
None (open label)
Enrolment
28 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03827954
Sponsor's protocol ID
PSC-1014-18
Other IDs
1R43NR018415-01
Acronym
HeartMapp
Status last verified
Aug 2021
First submitted
23 Jan 2019
Last updated
24 Aug 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Data of participants collected via REDCap will be made available to an unblinded research staff at Posit Science Corporation, San Francisco, CA, However, the PI to whom the grant is awarded will only have access to de-identified data.

Questions about this trial

What is this clinical trial studying?

A study testing HeartMapp+CT in people with Heart Failure and Cognitive Impairment, run by Posit Science Corporation at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 7 inclusion and 14 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Aug 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Primary outcome (Feasibility of HeartMapp+CT app usage) (time frame: 3-months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Aug 2021.

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