TrialReader


Working Memory Training for Dysphoric Students

NCT02184481 — Not applicable, Completed, 94 participants, Erasmus Medical Center

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

Working Memory Training to Decrease Depression, Anxiety and Rumination in Dysphoric Students

RegistryNCT02184481
StatusCompleted
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: double, treatment
Enrollment94 (Actual)
SponsorErasmus Medical Center (Other)
ConditionsDepression
InterventionsWorking memory training, Placebo training (Behavioral)
Datesstart 2013-09-01, primary completion 2014-06-01, first posted 2014-07-09, last updated 2014-07-09
Locations1 site in Netherlands

Related Papers Related Patents Related Grants Related Experts
AI Assistant Save
All trials for Depression All trials of Working memory training All trials of Placebo training

-Summary

Depression is associated with impairments in executive functions, including working memory (WM) which is needed to maintain and manipulate goal-relevant information. Due to these WM impairments depressed individuals have difficulties inhibiting and shifting from irrelevant (negative) information and updating goal relevant information. This study explored whether training WM decreases these impairments and reduces clinical symptoms of depression, anxiety and rumination. Sixty-one students with an elevated score on the BDI-II, representing a dysphoric mood state, executed a working memory training (n = 34) or placebo training (n = 27). Before and after training their depression, anxiety, rumination and working memory were assessed. Furthermore, they executed a working memory task while their pupil dilation was measured to assess their fatigue. Moreover, the investigators compared the dysphoric students with a healthy student population on all measures.

Expand all sections  ·  Collapse all

+Arms and interventions

ArmTypeInterventionsDescription
Working memory trainingExperimentalBehavioral: Working memory trainingParticipants executed the training for three weeks, three times a week, half an hour per session. The training was a game in which the participant was a person who had to become strong to fight with a fantasy figure. The person could become stronger when giving the right answers in eight different working memory tasks. The level adapted to the working memory capacity of the participant.
Placebo trainingPlacebo comparatorBehavioral: Placebo trainingParticipants executed the training for three weeks, three times a week, half an hour per session. The training was a game in which the participant was a person who had to become strong to fight with a fantasy figure. The person could become stronger when giving the right answers in eight different working memory tasks. The level in the placebo condition was easy and did not adapt to the working memory capacity of the participant.
  • Working memory training (Behavioral)
  • Placebo training (Behavioral)

+Outcome measures

Primary outcomes

  • Beck Depression Inventory Second Edition (BDI-II) score change between pre and post measurement [Pre training (baseline), post training (4 weeks after baseline, training starts 1 day after baseline)]: Depression is measured with the BDI-II

Secondary outcomes

  • State-Trait Anxiety Inventory (STAI) scores change from pre to post training measurement [Pre training (baseline), post training (4 weeks after baseline, training starts 1 day after baseline)]: The STAI measures state, trait and total anxiety

Other outcomes

  • Ruminative Response Scale (RRS) score change between pre and post training [Pre training (baseline), post training (4 weeks after baseline, training starts 1 day after baseline)]: The RRS measures rumination
  • Spanboard task [Pre training (baseline), post training (4 weeks after baseline, training starts 1 day after baseline)]: The Spanboard task measures working memory capacity
  • N-back task [Pre training (baseline), post training (6 weeks after baseline, training starts 1 day after baseline)]: The n-back task was assessed while participants pupil dilation was measured with the eyetracker. The aim of this measurement was to measure fatigue.

+Eligibility

Sex: All, ages: 17 Years to any, accepts healthy volunteers

Inclusion Criteria:

* BDI 10 of higher for dysphoric group
* BDI 5 or lower for healthy control group

+Locations (1)

FacilityCityCountryStatus
Erasmus University RotterdamRotterdam, South HollandNetherlands

+Publications

  • Results publication: Hopstaken JF, Wanmaker S, van der Linden D, Bakker AB. Does Dysphoria Lead to Divergent Mental Fatigue Effects on a Cognitive Task? PLoS One. 2015 Jun 15;10(6):e0130304. doi: 10.1371/journal.pone.0130304. eCollection 2015. PMID 26075389

My Notes