ACT-HF: Attention, Cognition and Self-Management in Heart Failure

NCT ID: NCT01064765

Last Updated: 2013-09-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

72 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-09-30

Study Completion Date

2011-03-31

Brief Summary

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This study is designed to determine if a relationship exists between problems with memory, attention, learning, insight and executive function and self management in heart failure.

Detailed Description

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Eligible participants are those 75 years of age or less, with left ventricular ejection fractions of 40% or less, english speaking and no known cognitive deficits. Participants will be administered the Repeatable Battery for the Assessment of Neuropsychological Status and the Controlled Oral Word Association test at the study visit. They will also be asked to complete the Self-Care in Heart Failure Index and the Anosognosia Questionnaire for Dementia at their convenience and mail back to investigator. Participants will be contacted in 90 days to determine if they have been hospitalized, and if so, for how many days.

Conditions

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Heart Failure

Keywords

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Heart failure Self management cognitive dysfunction Self management of heart failure

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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Heart failure

Outpatients with heart failure, age 75 or less, left ventricular ejection fraction 40% or less, english speaking with no known dementia

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* 75 years of age or less
* ejection fraction 40% or less
* heart failure 6 months or more
* English speaking
* no known dementia
* no active substance abuse
* presence of caregiver/support

Exclusion Criteria

* neurologic disorders potentially causing cognitive dysfunction
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sigma-Tau Research, Inc.

INDUSTRY

Sponsor Role collaborator

University of Chicago

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Savitri E. Fedson, MD

Role: PRINCIPAL_INVESTIGATOR

University of Chicago

Locations

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University of Chicago Medical Center

Chicago, Illinois, United States

Site Status

Countries

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United States

Other Identifiers

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16233A

Identifier Type: -

Identifier Source: org_study_id