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Clinical Trials/ISRCTN17767674
ISRCTN17767674
Completed
未知

Effects of Emotion Recognition Training on mood among individuals with high levels of depressive symptoms

niversity of Bristol (UK)0 sites190 target enrollmentSeptember 12, 2012
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ConditionsMood disordersMental and Behavioural DisordersUnspecified mood [affective] disorder

Overview

Phase
未知
Intervention
Not specified
Conditions
Mood disorders
Sponsor
niversity of Bristol (UK)
Enrollment
190
Status
Completed
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

  1. 2013 protocol in http://www.ncbi.nlm.nih.gov/pubmed/23725208 2. 2018 results in https://doi.org/10.1101/335042 (added 21/01/2019) 3. 2020 results in https://www.ncbi.nlm.nih.gov/pubmed/32063231 (added 21/02/2020)
Registry
who.int
Start Date
September 12, 2012
End Date
March 1, 2014
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversity of Bristol (UK)

Eligibility Criteria

Inclusion Criteria

  • •1\. Aged between 18 and 40 years
  • •2\. Participants who score 14 or higher on the Beck Depression Inventory (BDI)\-II
  • •3\. English as first language or equivalent level of fluency
  • •4\. Able to give informed consent as judged by lead researcher

Exclusion Criteria

  • •1\. Primary anxiety disorder, psychosis, bipolar disorder or substance dependence \[other than nicotine and caffeine] as defined by Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM\-IV)
  • •2\. Current use of illicit drug (except cannabis)
  • •3\. Being at clinically significant risk for suicidal behaviour
  • •4\. Use of psychotropic medication in last 5 weeks prior to study
  • •5\. Major somatic or neurological disorders and concurrent medication which could alter emotional processing (including active treatment with counselling, psychotherapy and cognitive behavioural therapy). We will allow intermittent use of medication, judged by the principal investigator.
  • •6\. Participants who in opinion of the lead researcher are not appropriate to participate

Outcomes

Primary Outcomes

Not specified

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