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Online Cognitive Control Training for Remitted Depressed Patients

NCT03278756 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2022-11-09

No results posted yet for this study

Summary

This study evaluates the effectiveness of an internet-delivered cognitive control training as a preventive intervention for remitted depressed patients. Half of the participants will receive a cognitive control training, while the other half will receive a low cognitive load training that acts as an active control condition.

Conditions

  • Major Depression in Remission

Interventions

BEHAVIORAL

Cognitive control training

10 sessions of an adaptive paced auditory serial addition task, each lasting 15 minutes, over the course of two weeks.

BEHAVIORAL

Active control training

10 sessions of an low cognitive load task, each lasting 15 minutes, over the course of two weeks.

Sponsors & Collaborators

  • University Ghent

    lead OTHER

Principal Investigators

  • Ernst HW Koster, PhD · University Ghent

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-09-01
Primary Completion
2019-03-13
Completion
2019-03-13

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 NCT03278756 on ClinicalTrials.gov