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Cognitive Training in Heart Failure Study (CogTrain-HF)

U

Universität des Saarlandes

Status

Completed

Conditions

Cognitive Impairment
Congestive Heart Failure

Treatments

Behavioral: Test of general knowledge
Behavioral: Cognitive training

Study type

Interventional

Funder types

Other

Identifiers

NCT02415517
CogTrain-HF

Details and patient eligibility

About

The daily routine in clinical settings often showed cognitive impairments in patients with congestive heart failure, particularly in terms of executive functions, episodic memory, perceptual speed and attention. It is assumed that cognitive impairments in patients with congestive heart failure may lead to deficits in medication-adherence and self-care abilities, resulting in increased healthcare costs. Recent studies reported performance improvements after cognitive training that transferred to new, untrained tasks and abilities in healthy subjects across a wide range of ages. This study investigates the effects of cognitive training in patients with congestive heart failure.

Full description

Cognitive functions of patients with congestive heart failure (NYHA II-III) before (pretest) and after (posttest) cognitive-training intervention are investigated. Changes in cognitive functions are compared to changes in two control groups: 1) age and gender matched active control group 2) age and gender matched passive waiting list control group.

The neuropsychological test battery applied at pretest and posttest includes measures of episodic memory, working memory, short-term memory, executive functions, perceptual speed and intelligence. In addition, the investigators apply standardized questionnaires of self-assessed quality of life, cognitive functioning in daily life, selfcare, and psychological well-being (depression, anxiety and personality). Relevant physiological data such as ejection fraction, heartrate, N-terminal pro brain natriuretic peptide (NT-pro-BNP) as well as drug blood level are recorded.

Enrollment

107 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Congestive heart failure
  • NYHA II-III

Exclusion criteria

  • Psychosis
  • Dementia
  • Major depression
  • Reanimation (<3month)
  • Patients with assist device system

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

107 participants in 3 patient groups

Experimental group
Experimental group
Description:
Intervention: Cognitive Training
Treatment:
Behavioral: Cognitive training
Active control group
Active Comparator group
Description:
Intervention: Test of general knowledge
Treatment:
Behavioral: Test of general knowledge
Passive control group
No Intervention group
Description:
No intervention

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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