An interventional study of Flash Version of EMDR in PTSD, sponsored by York University. Status unknown at 2 sites in Canada. Open to participants aged 20 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-01-04.
Sponsored by York University · Not applicable, Interventional, and Treatment
To assess the Flash version of EMDR in reductions of the disturbance of upsetting memories at post-intervention, and 1-month follow up within a double-blinded, online 2-arm randomized controlled trial (RCT) with self-report outcomes. We will assess 45 per group, adequate for the detection of a medium effect size.
This double-blinded, RCT will assess the comparative efficacy of these two online interventions designed to reduce memory disturbance.
This double-blinded, RCT compares the efficacy of 2 online interventions (Flash Version - EMDR; EMDR alone) designed to reduce memory disturbance.Inclusion Criteria: (1) approved for engagement assessment by the CloudResearch platform; (2) 25-60 years; 3) US-Canada residence; (4) a recalled disturbing memory of an event that has not repeated and was moderately upsetting, or greater when event occurred; (5) memory remains moderately upsetting or greater on recall. The disturbance of upsetting memories at post-intervention, and 1-month follow up will be assessed with self-report outcomes. We will assess 45 / group, adequate for the detection of a medium effect size. linked to an earlier memory (that is equally or more disturbing). Exclusion Criteria: Diagnosis of: (1) bipolar disorder; (2) borderline personality disorder; (3) obsessive compulsive disorder; (4) schizophrenia; (5) substance abuse/addiction in the past 3 months; (6) any suicidal ideation; (7) suicide attempt in the past 6 months. Interventions: Experimental participants observe video instructions of full FT, while controls receive an online intervention that follows traditional EMDR. Measures: Primary outcome: State Anxiety subscale of the State Trait Anxiety Inventory (STAI) at baseline, post-intervention, and after 1-month follow up; Post Traumatic Stress Disorder symptoms (PTSD) measured by PCL-5 (1 month follow up).
Secondary outcomes: the Subjective Units of Disturbance (SUDs) assessing change in immediately reported disturbance of recalled memories (baseline and post-intervention); depression measured by Patient Health Questionnaire (PHQ9) and Positive-Negative Affect measured by the Positive and Negative Affect Scale (PANAS).
York University is the lead sponsor of 51 studies on the registry; 12 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Flash methods (e.g. positive engaging focus) are used in addition to the standard EMDR techniques conveyed by video viewed online
Behavioral: Flash Version of EMDR
Use of standard EMDR techniques conveyed by video online
Behavioral: Flash Version of EMDR
EMDR and the inclusion of a positive engaging focus generated autonomously by participant
PTSD Checklist for DSM-5 (PCL-5) 1 - 44
Self Report Questionnaire
Time frame: 1 month follow up
State-Trait Anxiety Inventory - State 0 - 80.
Self Report Questionnaire
Time frame: 1 month follow up
Patient Health Questionnaire 0 - 27
Self Report Questionnaire
Time frame: 1 month follow up
Positive and Negative Affect Schedule 20 - 100
Self Report Questionnaire
Time frame: 1 month followup
Plan to share: Yes — Upon request, an anonymized data sheet (excel) will be sent
Supporting information: Study protocol, Sap, Icf, Csr
No publications or documents are linked to this record.
This study is status unknown, as verified in Feb 2022. You cannot join it, but the record below documents what was studied.
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York University