Cognitive Training in Heart Failure Study (CogTrain-HF)

NCT02415517 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 107

Last updated 2020-03-26

No results posted yet for this study

Summary

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.

Conditions

Interventions

BEHAVIORAL

Cognitive training

Cognitive training on computer. Six sessions with different tasks: "Tiere merken" \& "Räumlich visuelles Training" (application BrainTwister) and "Taskswitching" (programmed with eprime)

BEHAVIORAL

Test of general knowledge

Training of general knowledge on computer. Six sessions with different topics.

Sponsors & Collaborators

  • Deutsche Stiftung für Herzforschung

    collaborator OTHER
  • Universität des Saarlandes

    lead OTHER

Principal Investigators

  • Ingrid Kindermann, PD Dr.med. · University Hospital, Saarland

  • Julia Karbach, Prof. · Goethe-Universität Frankfurt am Main

  • Sonja Wedegärtner, Dipl.Psych. · University Hospital, Saarland

  • Maxie Bunz, Dipl.Psych. · University Hospital, Saarland

  • Michael Böhm, Prof. · University Hospital, Saarland

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2019-06-03
Completion
2019-12-04

Countries

  • Germany

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02415517 on ClinicalTrials.gov