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A Study on Better Cognitive Functioning Through Braintraining on the Internet

NCT04006756 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 38

Last updated 2021-12-01

No results posted yet for this study

Summary

This study evaluates the efficacy of an eight-week online cognitive training program on feasability and on objective and subjective cognitive functions in patients with late life mood disorders (LLMD). In the feasability study two training groups will be compared. The primary aim is to investigate feasability, measured by compliance attendance and satisfaction of the participants. The secondary aim is to study the possible effects of the intervention on cognitive functions. Additionally, effects on mood symptoms, social functioning, sense of mastery and quality of lide will be studied.

Conditions

  • Depression
  • Late Life Mood Disorder
  • Impaired Cognition
  • Alteration in Mood
  • Alteration in Cognition

Interventions

BEHAVIORAL

Online cognitive training 1

Eight-week online cognitive training program, three times a week for 45 minutes. The training contains several games that are designed to train cognitive functions.

BEHAVIORAL

Online cognitive training 2

Eight-week online active comparator program, three times a week for 45 minutes. The training contains several games.

Sponsors & Collaborators

  • Amsterdam UMC, location VUmc

    lead OTHER

Principal Investigators

  • Annemiek Dols, MD, PhD · Amsterdam UMC, location VUmc

  • Mardien Oudega, MD, PhD · Amsterdam UMC, location VUmc

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-17
Primary Completion
2021-11-11
Completion
2021-11-11

Countries

  • Netherlands

Study Locations

More Related Trials

Entities

Diseases

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 NCT04006756 on ClinicalTrials.gov