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Cognitive Control Training for Remitted Depressed Patients

NCT02407652 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2015-12-17

No results posted yet for this study

Summary

The purpose of this study is to explore the effectiveness of an internet-delivered cognitive control training as a preventive intervention for remitted depressed patients.

Conditions

  • Major Depression in Remission

Interventions

BEHAVIORAL

Cognitive Control Training

10 adaptive Paced Auditory Serial Addition Task (PASAT) sessions, 400 trials each

BEHAVIORAL

Low Cognitive Load Training

10 low cognitive load sessions, 400 trials each

Sponsors & Collaborators

  • University Ghent

    lead OTHER

Principal Investigators

  • Ernst Koster, PhD · University Ghent

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
23 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-31
Primary Completion
2015-10-31
Completion
2015-10-31

Countries

  • Belgium

Study Locations

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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 NCT02407652 on ClinicalTrials.gov