A Personalized Approach to Effects of Affective Bias Modification on Symptom Change and Rumination
Study Details
Study Description
Brief Summary
This study evaluates the effect of a computerized intervention for depressive symptoms called Affective Bias Modification (ABM). A third of the patients will receive active ABM, a third will receive sham ABM and a third will undergo assessment only. The study will investigate if rumination mediates the effect of the intervention and investigate if specific symptom profiles affect the effect of the intervention.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
A main aim of the project is to investigate how the effects of an ABM intervention on depressive symptoms are mediated by transdiagnostic rumination and how characteristics of the symptom network moderate these effects. The Affective Bias Modification Task (ABM) will be applied in a randomized controlled, double blind clinical trial with 6 months follow-up. Personalized networks are generated from prospective assessment of depression-related processes at baseline and follow-ups. Patients (n = 150) will be recruited from out-patient clinics at Diakonhjemmet Hospital, and randomized into one of three conditions: active, sham and assessment only. Patients aged 18-65 with depression (major depressive disorder) or bipolar disorder 2, with or without comorbid anxiety and/or alcohol use disorder will be included. The main hypothesis is that subjects who are in the active ABM group will exhibit less tendency for stress related (state) rumination compared to those in the placebo group. Active vs placebo ABM will decrease depressive symptoms (6 months) and this effect will be mediated by the change in state rumination. Densely connected symptom network and high strength centrality of rumination at baseline will moderate the effect of ABM. By combining mechanisms research with a personalized symptom network approach, this study will be in the forefront of understanding how a drug-free treatment option works and for whom it works best.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Active Affective Bias Modification Computer based Affective Bias Modification |
Behavioral: Affective bias modification
In the Affective bias modification (ABM) procedure, paired stimuli (e.g. a negative and a positive facial expression) are presented on a laptop screen, followed by one or two probes (dots) appearing in the spatial location of one of the stimuli. Participants are then required to press one of two buttons as quickly as possible to indicate the number of dots in the probe. Stimuli presentation time is 50% 500 ms and 50 % 1000 ms (evenly distributed throughout the task). In total, the ABM will comprise 90 trials of paired images of faces of different valences. In the active condition, the probe appears at the location of the most positive stimuli of each pair in 87 % of trials (encouraging a positive affective bias). Participants will do ABM in their homes (approx. 5 min.) twice a day for two weeks (28 sessions) using laptop computers provided by us.
Other Names:
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| Sham Comparator: Sham Affective Bias Modification Computer based sham Affective Bias Modification |
Behavioral: Sham Affective bias modification
In the Affective bias modification (ABM) procedure, paired stimuli (e.g. a negative and a positive facial expression) are presented on a laptop screen, followed by one or two probes (dots) appearing in the spatial location of one of the stimuli. Participants are then required to press one of two buttons as quickly as possible to indicate the number of dots in the probe. Stimuli presentation time is 50% 500 ms and 50 % 1000 ms (evenly distributed throughout the task). In total, the ABM will comprise 90 trials of paired images of faces of different valences. In the sham condition, the probe appears at the location of the most positive stimuli of each pair in 50 % of trials (no contingency between facial expressions shown and the probe location). Participants will do ABM in their homes (approx. 5 min.) twice a day for two weeks (28 sessions) using laptop computers provided by us.
Other Names:
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Outcome Measures
Primary Outcome Measures
- Self-reported depressive symptoms: Becks Depression Inventory-II [At 6 months follow-up]
Self-reported depressive symptoms 6 months after the ABM intervention based on a 21-item scale. Each item is scored 0-3 (where scoring description is adapted to each item), yielding a score from 0-63.
- State rumination: Brief State Rumination Inventory [At baseline and two weeks follow up]
Change in self-reported state rumination after stress induction on a 8 item scale. Each item is scored on a 0-100 Visual Analogue Scale, yielding a score from 0-800 will mediate the effect of ABM on depressive symptoms at six months follow up.
- State rumination: Brief State Rumination Inventory [At two weeks follow up.]
Self-reported state rumination after stress induction on a 8 item scale. Each item is scored on a 0-100 Visual Analogue Scale, yielding a score from 0-800.
Secondary Outcome Measures
- Affective bias: Dot-probe task [From baseline to two weeks follow up]
Change in reaction time to probes in the location of the positive facial stimuli.
- Symptom network change: experience sampling of depressive symptoms [From two weeks prior to baseline to two weeks after two weeks follow up.]
Less densely connected network of self-reported symptoms and changed centrality of rumination based on a 9-item experience sampling questionnaire administrated five times/day for two periodes of fourteen days. Each item is scored on a 0-100 visual analogue scale.
- Symptom network: experience sampling of depressive symptoms [At two weeks prior to baseline.]
Network density of self-reported symptoms and centrality of rumination prior to baseline will moderate the effect of ABM, based on a 9-item experience sampling questionnaire administrated five times/day for fourteen days. Each item is scored on a 0-100 visual analogue scale.
Eligibility Criteria
Criteria
Inclusion Criteria:
- Current or remitted Major Depressive Disorder, with or without anxiety, with or without alcohol use disorder
Exclusion Criteria:
- Neurological disorder, mania, and/or psychosis.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Department of Psychology | Oslo | Norway | 0317 |
Sponsors and Collaborators
- University of Oslo
- Extrastiftelsen
- Diakonhjemmet Hospital
- University of Oxford
Investigators
- Principal Investigator: Nils Inge Landrø, Dr.Philos, University of Oslo
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 2019/FO249225