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Clinical Trials/NCT02119975
NCT02119975CompletedNot Applicable

A Working Memory Training to Decrease Rumination in Depressed and Anxious Individuals: A Double-blind Randomized Controlled Trial

Erasmus Medical Center1 site in 1 country98 target enrollmentStarted: August 1, 2011Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
98
Locations
1
Primary Endpoint
Change in Ruminative Response Scale (RRS) score from pre to post training and after two months (follow up 2)

Study Overview

Brief Summary

Dysfunctioning executive functioning, including working memory (WM), is related to rumination. Findings show that working memory capacity (WMC) can be increased by training. The current study explored by means of a double-blind randomized controlled trial whether an adaptive WM training could reduce rumination, anxiety and depression in a sample of 98 depressed and anxious individuals.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
18 Years to 67 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Major depression diagnosis
  • •Anxiety diagnosis

Exclusion Criteria

  • •Current psychosis
  • •Substance abuse

Arms & Interventions

Placebo working memory training

Placebo Comparator

Intervention: Placebo training (Behavioral)

Working memory training

Experimental

Intervention: Working memory training (Behavioral)

Outcomes

Primary Outcomes

Change in Ruminative Response Scale (RRS) score from pre to post training and after two months (follow up 2)

Time Frame: Pre training (baseline), post training (4 weeks after baseline, training starts 1 day after baseline) and follow-up (2 months after post-test)

Dutch version; Raes, Hermans, \& Eelen, 2003) measures the frequency of self-reported rumination behavior, with answer options ranging from 1 (never) to 4 (always). The total score of the 22 items was used in the analyses.

Secondary Outcomes

  • Change in Beck Depression Inventory Second Edition (BDI-II) score from pre to post training and after two months (follow up 2)(Pre training (baseline), post training (4 weeks after baseline, training starts 1 day after baseline) and follow-up (2 months after post-test))
  • Change in State-Trait Anxiety Inventory (STAI) score from pre to post training and after two months (follow up 2)(Pre training (baseline), post training (4 weeks after baseline, training starts 1 day after baseline) and follow-up (2 months after post-test))

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ingmar Franken

Professor

Erasmus Medical Center

Study Sites (1)

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