Cognitive Intervention to Improve Memory in Heart Failure Patients (Memoir-HF)

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Indiana University

Status

Completed

Conditions

Heart Failure NYHA Class II
Heart Failure NYHA Class III
Heart Failure NYHA Class I

Treatments

Behavioral: Computerized Crossword Puzzles
Behavioral: Computerized Cognitive Training with Brain HQ

Study type

Interventional

Funder types

Other

Identifiers

NCT03035565
R01NR016116-01A1

Details and patient eligibility

About

Cognitive Intervention to Improve Memory in Heart Failure patients

Full description

A three arm randomized controlled trial of 276 heart failure patients.

Enrollment

276 patients

Sex

All

Ages

21+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • At least 21 years of age
  • Understands English
  • Has access to a telephone
  • Hears normal conversation
  • For patients with hearing aids, able to wear and hear through headsets
  • Diagnosis of chronic heart failure, stage C, NYHA I, II or III
  • Receiving guideline derived medical therapy
  • Heart failure validated by echocardiography or other method in past 2 years
  • Able to read a computer screen with or without glasses or lenses

Exclusion criteria

  • History of drug or alcohol abuse or major psychiatric diagnosis present before the heart failure diagnosis
  • Alzheimer or other dementia diagnosis or central nervous system degenerative disorder
  • Terminal cancer
  • Patients with baseline Montreal Cognitive Assessment (MoCA) score of less than 19

Supplement Eligibility: First 144 patients randomized in the parent trial.

Trial design

276 participants in 3 patient groups

Computerized Cognitive Training Brain HQ
Experimental group
Description:
Computerized cognitive training intervention using Brain HQ initiated and continued 1 hour/day, 5 days/week for 8 weeks
Treatment:
Behavioral: Computerized Cognitive Training with Brain HQ
Computerized Crossword Puzzles
Active Comparator group
Description:
General cognitive stimulation puzzles intervention initiated and continued 1 hour/day, 5 days/week for 8 weeks
Treatment:
Behavioral: Computerized Crossword Puzzles
Usual Care
No Intervention group
Description:
No computerized cognitive intervention

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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