The hypothesis is not public yet, because of the quality of the study.
ID
Bron
Aandoening
Major Depressive Disorder (MDD)
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
For testing the main hypothesis, that IBM is able to reduce depressive symptom levels, the Beck’s Depression Inventory II (BDI) will be used.
Achtergrond van het onderzoek
The summary is not public yet, because of the quality of the study.
Doel van het onderzoek
The hypothesis is not public yet, because of the quality of the study.
Onderzoeksopzet
Primary outcome measure
-BDI (baseline, 2 weeks, 1 month, 6 months, 12 months)
Secondary outcome measures
-AST (baseline, 2 weeks, 1 month)
-PIT (baseline, 1 month, 6 months)
-IDS-SR (baseline, 1 months, 6 months, 12 months)
-STAI (baseline, 1 month, 6 months)
-SUIS (baseline, 1 month, 6 months)
-DAS (baseline, 1 month, 6 months)
-EQ (baseline, 1 month)
-TIC-P (baseline, 1 month, 6 months, 12 months)
-EQ-5D (baseline, 1 month, 6 months, 12 months)
-MINI (baseline, 12 months)
-Patient satisfaction questionnaire (1 month, 6 months)
-Patient satisfaction interview (12 months)
-Demographic items (baseline, 1 month)
Onderzoeksproduct en/of interventie
Interpretation Bias Modification (IBM)
Patients will be offered IBM when just starting their treatment (maximum of 4 sessions) or when waitlisted for treatment, accompanied or followed by further indicated care. IBM entails 10 20-minute computer training sessions over the course of 4 weeks: 7 daily sessions during in week 1, followed by weekly sessions during the following 3 weeks. The first session will be completed at Pro Persona. All other sessions will be completed via the internet at home.
Both groups will receive a mixture of auditory and picture-word training sessions.
Not all of the information about the intervention is public yet, because of the quality of the study.
Algemeen / deelnemers
Tarweweg 2
Denise te Paste
Nijmegen 6534 AM
The Netherlands
-
D.tepaste@psych.ru.nl
Wetenschappers
Tarweweg 2
Denise te Paste
Nijmegen 6534 AM
The Netherlands
-
D.tepaste@psych.ru.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
-A diagnosis of major depressive disorder, first or recurrent according to the DSM- IV-TR (APA; American Psychiatric Association, 2000), as assessed with the MINI
-18-65 years old
-Provides informed consent
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
-Any psychotic disorder (current or previous)
-Current mania or hypomania or a history of bipolar disorder
-Cognitive disabilities (IQ < 80)
-Visual disabilities that interfere with a computer task
-Acute suicidal risk
-No sufficient command of Dutch language to participate in the study
-Lack of sufficient experience with the use of computers (based on subjective
estimation of the patient)
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL5786 |
NTR-old | NTR5949 |
CCMO | NL55683.091.15 |
OMON | NL-OMON47198 |