- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05269433
The Effect of Attention Training on Symptoms and Emotion Regulation in Depressive Patients
The Effect of Attention Training on Symptoms and Emotion Regulation in Depressive Patients: Validation of the Online Contingent Attention Training (OCAT).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Sint-Denijs-Westrem, Belgium, 9051
- KARUS
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Oost-Vlaanderen
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Gent, Oost-Vlaanderen, Belgium, 9000
- Ghent University
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Vlaams-Brabant
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Tienen, Vlaams-Brabant, Belgium, 3300
- Alexianen PK Zorggroep Tienen
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Diagnosis of depressive disorder
- Admission to a psychiatric hospital (Alexianen PK, Tienen)
Exclusion Criteria:
- Current psychotic disorder
- Current neurological impairments
- Current alcohol addiction
- Current treatment with antidepressants that has not yet been kept constant
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: PSE + OCAT-sham
Psycho-education video + an active placebo training consisting of 10 sessions of ±12 minutes each (during an intervention period of two weeks) will be administered.
The training task is an undirected scrambled sentences task with online contingent feedback (only) on the speed with which the sentences were made.
In this condition, participants will not receive feedback on emotional attention.
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Placebo version of the online contingent attention training preceded by a psycho-education movieclip.
All groups watch a psycho-education video before the start of the 10-day attention training.
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Experimental: PSE + OCAT
Psycho-education video + an attention training consisting of 10 sessions of ±12 minutes each (during an intervention period of two weeks) will be administered.
The training task is a positively directed scrambled sentences task with online contingent feedback on how much attention was paid to positive vs. negative words (emotional attention), along with feedback on the speed with which the sentences were made.
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All groups watch a psycho-education video before the start of the 10-day attention training.
Online contingent attention training preceded by a psycho-education movieclip.
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Experimental: PSE + OCAT+
Psycho-education video + short motivational video before each training session + an attention training consisting of 10 sessions of ±12 minutes each (during an intervention period of two weeks) will be administered.
The training task is a positively directed scrambled sentences task with online contingent feedback on how much attention was paid to positive vs. negative words (emotional attention), along with feedback on the speed with which the sentences were made.
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All groups watch a psycho-education video before the start of the 10-day attention training.
Online contingent attention training preceded by a psycho-education movieclip.
Participants in the OCAT+ condition watch a short motivational video before each training session.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Changes in depression symptoms
Time Frame: pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Measured by the Depression and Anxiety Stress Scale (DASS-21), a self report questionnaire containing 21 items to measure the severity of a range of common symptoms for depression, anxiety and stress.
Participants are required to indicate the presence of a symptom over the previous week.
Each item of the questionnaire is scored from 0 (did not apply to me at all) to 3 (applied to me very much or most of the time).
Higher scores indicate more symptoms.
The questionnaire comprises three subscales (Depression, Anxiety, and Stress).
For this specific outcome measure, the depression subscale will be used (7 items) to investigate the specific effects of the training on depressive symptoms.
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pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Changes in anxiety symptoms
Time Frame: pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Measured by the Depression and Anxiety Stress Scale (DASS-21), a self report questionnaire containing 21 items to measure the severity of a range of common symptoms for depression, anxiety and stress.
Participants are required to indicate the presence of a symptom over the previous week.
Each item of the questionnaire is scored from 0 (did not apply to me at all) to 3 (applied to me very much or most of the time).
Higher scores indicate more symptoms.
The questionnaire comprises three subscales (Depression, Anxiety, and Stress).
For this specific outcome measure, the anxiety subscale will be used (7 items) to investigate the specific effects of the training on anxiety symptoms.
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pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Changes in stress symptoms
Time Frame: pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Measured by the Depression and Anxiety Stress Scale (DASS-21), a self report questionnaire containing 21 items to measure the severity of a range of common symptoms for depression, anxiety and stress.
Participants are required to indicate the presence of a symptom over the previous week.
Each item of the questionnaire is scored from 0 (did not apply to me at all) to 3 (applied to me very much or most of the time).
Higher scores indicate more symptoms.
The questionnaire comprises three subscales (Depression, Anxiety, and Stress).
For this specific outcome measure, the stress subscale will be used (7 items) to investigate the specific effects of the training on stress symptoms.
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pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Changes in cognitive emotion regulation strategies
Time Frame: pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Measured by the Cognitive Emotion Regulation Questionnaire (CERQ), a self-report questionnaire measuring different emotion regulation strategies, containing 36 items with a 5-point Likert response format scored from 1 ("Almost never") to 5 ("Almost always").
This questionnaire has 9 sub-scales: self-blame, other-blame, rumination, catastrophizing, putting into perspective, positive refocusing, positive reappraisal, acceptance and refocus on planning.
Each sub-scale has a scoring range between 4 and 20.
A higher score represents a greater frequency of engaging in that emotion regulation strategy.
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pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Self-Esteem
Time Frame: pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Measured by the Rosenberg Self Esteem Scale (RSES), a self-report questionnaire assessing global self-esteem.
The questionnaire consists of 10 items with five positively worded items and five negatively worded.
Four response categories are used, with items scored from 0 (Strongly Disagree) to 3 (Strongly Agree).
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pre-test (before starting the training), post-test (immediately after the training), follow-up (three months after the training)
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Treatment Credibility and Expectancy
Time Frame: pre-test (before starting the training), post-test (immediately after the training)
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Measured by the Credibility/Expectancy Questionnaire (CEQ).
It measures participants' credibility and expectancy of the training.
In the credibility scale, 4 items are rated on 9-point scales ranging from 1 (Not at all logical/useful/confident) to 9 (Very logical/effective/confident).
This leads to a total score on this scale between 3 and 27.
In the expectancy scale (2 items) the same 9-point scale is used, along with an 10-point scale (from 1% to 100%).
Responses are standardized to get the total expectancy score.
Higher scores represent higher credibility and expectancy.
In this version of the CEQ, an extra item is included containing the question if the participant believes to be part of the placebo condition (to be responded with 'yes/no').
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pre-test (before starting the training), post-test (immediately after the training)
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Changes in emotional attention
Time Frame: pre-test (before starting the training), post-test (immediately after the training)
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Measured by a baseline measure in the OCAT app. Participants perform a Scrambled Sentences Task to measure pre-post changes in emotional attention biases. Participants are instructed to unscramble the sentences as fast as possible to form the first grammatically correct and meaningful positive or negative sentence that spontaneously came to their mind, using only 5 words. Participants are asked to press a fixation cross to start the reading section of the SST. Then, 6 words are hidden into individual squares and participants move their fingers to uncover and read the corresponding word. When participants move their fingers away from one word to the position of another word, the previous word is hidden again and the next word is shown. The position and coordinates of the participants' finger on the screen allow us to monitor the exact time that participants are attending and reading each word, and thus to measure attention biases towards negative and positive words. |
pre-test (before starting the training), post-test (immediately after the training)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Rudi De Raedt, Professor, University Ghent
Publications and helpful links
General Publications
- Sanchez-Lopez A, Everaert J, Van Put J, De Raedt R, Koster EHW. Eye-gaze contingent attention training (ECAT): Examining the causal role of attention regulation in reappraisal and rumination. Biol Psychol. 2019 Mar;142:116-125. doi: 10.1016/j.biopsycho.2019.01.017. Epub 2019 Feb 5.
- De Raedt R, Hooley JM. The role of expectancy and proactive control in stress regulation: A neurocognitive framework for regulation expectation. Clin Psychol Rev. 2016 Apr;45:45-55. doi: 10.1016/j.cpr.2016.03.005. Epub 2016 Mar 24.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0G054-2021-07
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
- Individual participant data will not be available.
- Other documents will be available: Statistical Analysis Plan, Study Protocol (upon request to the researchers).
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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