No registrations found.
ID
Source
Brief title
Health condition
Suicidal, intrusions, mental problems, depression,
Sponsors and support
Intervention
Outcome measures
Primary outcome
Feasibility (measured by i.e. treatment adherence and data collection using online questionnaires)
Secondary outcome
Suicidal ideation (BSSI, SIDAS), depressive symptoms (BDI-II), suicidal intrusions (SINAS), Psychological distress (BSI)
Background summary
Suicide is a major public health problem, and it remains unclear which processes link suicidal plans to the act of suicide. Growing evidence shows that the majority of suicidal patients diagnosed with major depression or bipolar disorder report repetitive suicide-related images and thoughts. In addition, experimental and clinical studies show that vividness of negative as well as positive intrusive images may be reduced by Dual Task (e.g. eye movements) interventions taxing the working memory. We propose that the eye movements during image retrieval will also reduce intensity and frequency of suicidal imagery.
The current registration is for the pilot trial, a preliminary study set up to evaluate feasibility, potential adverse events, and implementation of the (EMDT) intervention, to inform a full-scale, definitive randomized controlled trial.
Study participants are 6 depressed adults (18 years and older) with suicidal ideation. Participants will receive (max.) 6 sessions of EMDT as an add-on treatment to their care-as-usual.
The main study parameter will be the feasibility (i.e. treatment adherence, data collection) of setting up a multi-center randomized controlled trial evaluating the add-on Eye Movement Dual Task (EMDT) treatment.
Study objective
The pilot study has the following objectives associated to the preparations of a full-scale randomized controlled trial:
1. To evaluate the feasibility, acceptability, and implementation of the add-on Eye Movement Dual Task (EMDT) treatment
2. To test for potential adverse events and use this knowledge to create a safety protocol
Study design
Baseline (Intrusion Interview)
During treatment (max. 6 weeks)
Post-treatment
Intervention
EMDT add-on treatment
The treatment will be an add-on module that addresses intrusive suicidal images and can be added to regular treatment. It will consist of max. six sessions each of approximately 1 hour, in the course of three to six weeks, delivered at the participants’ mental health care center.
Eligible suicidal intrusion
The flash-forward/suicidal intrusion eligible to be treated by the EMDT treatment must score high on burdensomeness as measured by the Intrusion Interview. If the suicidal intrusion is interpreted as positive, i.e. if it’s used as a coping strategy, it is no longer eligible. In other words, the image may not present a desired situation that is attractive to the patient.
Each session will consist of the following steps:
1. Selection of intrusive suicidal flash-forward target images with related ideation (as informed by the baseline intrusion interview).
2. Consecutive set of eye movements of approximately 24 seconds by 10 second breaks. Between the sets, subjective units of distress scale (SUDS, scale 0-10) are administered to assess level of distress during imagery.
3. If the image still produces stress, the dual task procedure will be repeated for the target.
4. This procedure is repeated for all target images until all SUDS are at approximately 0.
The patients are receiving care-as-usual treatments during the course of the pilot study. Care-as-Usual for depression within the participating mental health care institution typically consists of (evidence-based) psychotherapy and/or antidepressant treatment.
Jaël Bentum, van
Van der Boechorststraat 1
Amsterdam 1081 BT
The Netherlands
+31 20 598 6615
j.s.van.bentum@vu.nl
Jaël Bentum, van
Van der Boechorststraat 1
Amsterdam 1081 BT
The Netherlands
+31 20 598 6615
j.s.van.bentum@vu.nl
Inclusion criteria
a. Have a minimum age of 18 years
b. Score >20 on the Beck Depression Inventory
c. Have suicidal ideation: score >20 on Suicidal Ideation Attributes Scale (SIDAS)
d. Currently receiving treatment (Care-as-usual) at GGZ InGeest Amsterdam
e. Adequate proficiency in the Dutch language
f. Have suicidal intrusions (as measured through the Intrusion Interview) that are experienced as a burden
Exclusion criteria
a. DSM-IV Psychotic disorder diagnosis
b. DSM-IV Depression with psychotic features diagnosis
c. DSM-IV Bipolar disorder diagnosis
d. High dropout risk (i.e. poor response rate when trying to get in contact with potential participant)
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL6946 |
NTR-old | NTR7202 |
Other | : METC protocol no. NL60318.028.17 (Phase 1) |