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A Comparison of Magnetic Resonance Imaging in Persons With Heart Failure to Health, Aged Matched Controls

A Comparison of Magnetic Resonance Imaging in Persons With Heart Failure to Health, Aged Matched Controls (MIND-HF)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02572648
Acronym
MIND-HF
Enrollment
30
Registered
2015-10-09
Start date
2015-10-31
Completion date
2017-08-31
Last updated
2017-09-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

Cardiomyopathy, Magnetic Resonance Imaging (MRI)

Brief summary

The purpose of this study is to examine the relation between the structural brain changes associated with heart failure, neurocognitive performance, and how these changes impact self-care behaviors.

Detailed description

The purpose of this study is use neuroimaging techniques to better understand the underlying structural brain changes and physiological mechanisms that guide the thinking and decision making processes required for people with heart failure. The study will compare how the underlying brain structures and circulation are similar to or different in persons with heart failure to healthy, aged matched controls using special neuroimaging procedures.

Interventions

OTHERBrain Imaging (Neuroimaging)

Magnetic Resonance Imaging (MR) will be acquired on a research dedicated Siemens 3Tesla TIM TRIO MRI scanner with a 32-channel head coil.The MRI scanning protocol will have scans to measure voxelwise and whole-brain measures of grey matter (GM) volumes through a high resolution T1-weighted (T1W) multi-echo magnetization prepared gradient echo (MEMPRAGE) anatomic scan. Total time in scanner will be approximately 53 minutes.

OTHERCognitive Function Assessment

Cognitive function will be assessed using several batteries; the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS), the Controlled Oral Word Association Test (COWA), the Color Trails 1 & 2, the WAIS-III Digit Span and Letter Number Sequence test, the Stroop Test, and the California Computerized Assessment Package Reaction Time test (CALCAP).

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
Emory University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

Participants with heart failure: * Speak and understand English * Live independently within a 60 mile radius of Atlanta * Montreal Cognitive Assessment (MOCA) score of less than or equal to 24 * Documented medical diagnosis of New York Heart Association (NYHA) class II or III systolic * Left ventricular ejection fraction (LVEF) greater than or equal to 10% that is documented within the last year by echocardiogram, cardiac catheterization ventriculography, or radionuclide ventriculography * Receiving medication therapy for heart failure (HF) according to American College of Cardiology (ACC) American Heart recommendation guidelines for at least 8 weeks prior to study enrollment Healthy Controls * Speak and understand English * Live independently within a 60 mile radius of Atlanta

Exclusion criteria

Participants with heart failure: * New York Heart Association (NYHA) class I or IV * Change in heart failure (HF) therapy within 6 months * Worsening of heart failure (HF) symptoms within last 5 days * Unstable angina * Renal insufficiency (serum creatinine greater than 3.o mg/dL) * Hospitalized within the last 30-days * Diagnosed with any neurological disorder that may interfere with cognitive function * Beck Depression Inventory II (BDI-II) score greater than 25 * Claustrophobia * Implanted devices such as internal cardiac defibrillator or pacemaker * Carrying non-removable objects * Stents * Body weight more than 120 kg Healthy Controls * Taking prescription medications * Cardiovascular disease; * Cerebrovascular disease * Neurological disease * Respiratory disease * Claustrophobia * Any implanted metal objects not considered safe or appropriate for the MRI environment.

Design outcomes

Primary

MeasureTime frameDescription
Structural White MatterVisit 1 (Up to 2 hours)Diffusion tensor imaging (DTI) and myelin water imaging (MWI) will be used to compare brain structural white matter between participants with heart failure and healthy controls. This will be obtained via magnetic resonance imaging (MRI) techniques.

Secondary

MeasureTime frameDescription
Global Cerebral Blood Flow (CBF)Visit 1 (Up to 2 hours)Arterial spin labeling (ASL) based magnetic resonance (MR) perfusion imaging will evaluate global cerebral blood flow (CBF). This will be obtained via magnetic resonance imaging (MRI) techniques.
Regional Cerebral Blood Flow (CBF)Visit 1 (Up to 2 hours)Arterial spin labeling (ASL) based magnetic resonance (MR) perfusion imaging will evaluate regional cerebral blood flow (CBF). This will be obtained via magnetic resonance imaging (MRI) techniques.
Structural Grey MatterVisit 1 (Up to 2 hours)Voxel-based morphometry (VBM) of T1-weighted (T1w) high-resolution magnetic resonance imaging MRI anatomics will be used to measure brain structural white matter.
Cognitive Function assessed by the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)Visit 2 (Up to 2 hours)The Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) is a brief, individually administered test designed to evaluate neuropsychological status of adults, ages 20-89. The 12 subtests measure attention, language, visuospatial/constructional abilities, and immediate and delayed memory.
Cognitive Function assessed by the Controlled Oral Word Association (COWA) TestVisit 2 (Up to 2 hours)The Controlled Oral Word Association (COWA) Test is a verbal fluency test that measures spontaneous production of words belonging to the same category or beginning with some designated letter. The more words produced in the allotted time period the higher the score.
Cognitive Function assessed by the Color Trails TestVisit 2 (Up to 2 hours)The Color Trails Test measures sustained attention and sequencing. For Part 1, the respondent uses a pencil to rapidly connect circles numbered 1-25 in sequence. For Part 2, the respondent rapidly connects numbered circles in sequence, but alternates between pink and yellow. The length of time to complete each trial is recorded, along with qualitative features of performance indicative of brain dysfunction, such as near-misses, prompts, number sequence errors, and color sequence errors.
Functional ConnectivityVisit 1 (Up to 2 hours)Functional connectivity that regulates neurocognitive functions will be assessed by blood oxygen level dependent resting state functional MRI (rsFMRI).This will be obtained via magnetic resonance imaging (MRI) techniques.
Cognitive Function assessed by the Wechsler Adult Intelligence Scale-III (WAIS-III) Letter Number Sequence TestVisit 2 (Up to 2 hours)During the Wechsler Adult Intelligence Scale-III (WAIS-III) Letter Number Sequence Test, participants will be presented with combinations of letters and numbers, (two to nine letter-number combinations). Participants will be asked to repeat each series by, first, repeating the numbers in ascending order, then the letters in alphabetical order. The test measures working memory or the ability to simultaneously recall and organize stimuli of different and similar types
Cognitive Function assessed by the Stroop TestVisit 2 (Up to 2 hours)The Stroop Test measure a person's selective attention capacity and skills, as well as their processing speed ability.It is used to examine a person's executive processing abilities. The Stroop Test during brain imaging studies is used to investigate regions of the brain that are involved in planning, decision-making, and managing real-world interference
Cognitive Function assessed by the California Computerized Assessment Package (CALCAP)Visit 2 (Up to 2 hours)The California Computerized Assessment Package assesses reaction times, speed of information processing, rapid visual scanning, form discrimination, brief memory and divided attention.
Self-Management assessed by the Self-care Index Heart Failure (SCHFI)Visit 2 (Up to 2 hours)The Self-care Index Heart Failure (SCHFI) is a measure designed to assess self-care maintenance, management, and confidence. Participants will be asked to recall feelings of the aforementioned in the last three months.
Peak oxygen consumption assessed by the Modified Balke TestVisit 2 (Up to 2 hours)Peaked oxygen consumption will be assessed by the Modified Balke Test. Participants will be asked to walk on a slightly inclined treadmill. The amount of oxygen consumed will be measured while walking for up to ten minutes.
Quality of Life assessed by the Kansas City Cardiomyopathy QuestionnaireVisit 2 (Up to 2 hours)The Kansas City Cardiomyopathy Questionnaire is a 23-item, self-administered instrument that quantifies physical function, symptoms (frequency, severity and recent change), social function, self-efficacy and knowledge, and quality of life.
Cognitive Function assessed by the Wechsler Adult Intelligence Scale-III (WAIS-III) Digit Span TestVisit 2 (Up to 2 hours)The Wechsler Adult Intelligence Scale-III (WAIS-III) Digit Span Test measures short-term memory, attention, and concentration. Participants will be asked to repeat 3 - 9 digits forward and 2 - 9 digits backwards.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026