A mixed‐methods, randomized controlled feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM‐5 Posttraumatic Stress Disorder (PTSD) in adults with intellectual disabilities

Objective To report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM‐5 posttraumatic stress disorder (PTSD) in adults with intellectual disabilities. Method A total of 29 participants were ra...

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Vydáno v:Journal of applied research in intellectual disabilities Ročník 32; číslo 4; s. 806 - 818
Hlavní autoři: Karatzias, Thanos, Brown, Michael, Taggart, Laurence, Truesdale, Maria, Sirisena, Chammy, Walley, Robert, Mason‐Roberts, Susan, Bradley, Aoife, Paterson, Douglas
Médium: Journal Article
Jazyk:angličtina
Vydáno: England Wiley Subscription Services, Inc 01.07.2019
Témata:
Adult
Clinical trials
Desensitization
Desensitization (Psychology)
Diagnostic and Statistical Manual of Mental Disorders
Evidence-based medicine
eye movement desensitization and reprocessing
Eye Movement Desensitization Reprocessing - methods
Eye movements
Feasibility Studies
Female
Follow-Up Studies
Humans
Intellectual disabilities
Intellectual Disability
Male
Middle Aged
Mixed methods research
Motor Reactions
Outcome Assessment, Health Care
Post traumatic stress disorder
Posttraumatic Stress Disorder
Psychotherapy
Qualitative Research
randomized feasibility study
Single-Blind Method
Stress Disorders, Post-Traumatic - therapy
United Kingdom > UK
randomized feasibility study
eye movement desensitization and reprocessing
intellectual disability
posttraumatic stress disorder
ISSN:1360-2322, 1468-3148, 1468-3148
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Abstract Objective To report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM‐5 posttraumatic stress disorder (PTSD) in adults with intellectual disabilities. Method A total of 29 participants were randomized to either to EMDR + SC (n = 15) or SC (n = 14). Participants completed measures on traumatic stress (PCL‐C) and comorbid distress at baseline, 1 week post‐treatment and 3‐month follow‐up. Results In the EMDR + SC group, 9 (60%) participants at post‐treatment and 7 (47%) participants at 3‐month follow‐up were diagnosis free. In SC, 4 (27%) at post‐treatment and follow‐up were diagnosis free. At post‐treatment, three participants (20%) dropped out from the EMDR + SC group, and 1 (7%) dropped out from the SC group. Conclusions It is feasible, acceptable and potentially effective to deliver EMDR in this population group.
AbstractList To report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM-5 posttraumatic stress disorder (PTSD) in adults with intellectual disabilities.OBJECTIVETo report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM-5 posttraumatic stress disorder (PTSD) in adults with intellectual disabilities.A total of 29 participants were randomized to either to EMDR + SC (n = 15) or SC (n = 14). Participants completed measures on traumatic stress (PCL-C) and comorbid distress at baseline, 1 week post-treatment and 3-month follow-up.METHODA total of 29 participants were randomized to either to EMDR + SC (n = 15) or SC (n = 14). Participants completed measures on traumatic stress (PCL-C) and comorbid distress at baseline, 1 week post-treatment and 3-month follow-up.In the EMDR + SC group, 9 (60%) participants at post-treatment and 7 (47%) participants at 3-month follow-up were diagnosis free. In SC, 4 (27%) at post-treatment and follow-up were diagnosis free. At post-treatment, three participants (20%) dropped out from the EMDR + SC group, and 1 (7%) dropped out from the SC group.RESULTSIn the EMDR + SC group, 9 (60%) participants at post-treatment and 7 (47%) participants at 3-month follow-up were diagnosis free. In SC, 4 (27%) at post-treatment and follow-up were diagnosis free. At post-treatment, three participants (20%) dropped out from the EMDR + SC group, and 1 (7%) dropped out from the SC group.It is feasible, acceptable and potentially effective to deliver EMDR in this population group.CONCLUSIONSIt is feasible, acceptable and potentially effective to deliver EMDR in this population group.
To report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM-5 posttraumatic stress disorder (PTSD) in adults with intellectual disabilities. A total of 29 participants were randomized to either to EMDR + SC (n = 15) or SC (n = 14). Participants completed measures on traumatic stress (PCL-C) and comorbid distress at baseline, 1 week post-treatment and 3-month follow-up. In the EMDR + SC group, 9 (60%) participants at post-treatment and 7 (47%) participants at 3-month follow-up were diagnosis free. In SC, 4 (27%) at post-treatment and follow-up were diagnosis free. At post-treatment, three participants (20%) dropped out from the EMDR + SC group, and 1 (7%) dropped out from the SC group. It is feasible, acceptable and potentially effective to deliver EMDR in this population group.
ObjectiveTo report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM‐5 posttraumatic stress disorder (PTSD) in adults with intellectual disabilities.MethodA total of 29 participants were randomized to either to EMDR + SC (n = 15) or SC (n = 14). Participants completed measures on traumatic stress (PCL‐C) and comorbid distress at baseline, 1 week post‐treatment and 3‐month follow‐up.ResultsIn the EMDR + SC group, 9 (60%) participants at post‐treatment and 7 (47%) participants at 3‐month follow‐up were diagnosis free. In SC, 4 (27%) at post‐treatment and follow‐up were diagnosis free. At post‐treatment, three participants (20%) dropped out from the EMDR + SC group, and 1 (7%) dropped out from the SC group.ConclusionsIt is feasible, acceptable and potentially effective to deliver EMDR in this population group.
Objective To report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM‐5 posttraumatic stress disorder (PTSD) in adults with intellectual disabilities. Method A total of 29 participants were randomized to either to EMDR + SC (n = 15) or SC (n = 14). Participants completed measures on traumatic stress (PCL‐C) and comorbid distress at baseline, 1 week post‐treatment and 3‐month follow‐up. Results In the EMDR + SC group, 9 (60%) participants at post‐treatment and 7 (47%) participants at 3‐month follow‐up were diagnosis free. In SC, 4 (27%) at post‐treatment and follow‐up were diagnosis free. At post‐treatment, three participants (20%) dropped out from the EMDR + SC group, and 1 (7%) dropped out from the SC group. Conclusions It is feasible, acceptable and potentially effective to deliver EMDR in this population group.
Author Karatzias, Thanos
Truesdale, Maria
Bradley, Aoife
Walley, Robert
Sirisena, Chammy
Brown, Michael
Mason‐Roberts, Susan
Paterson, Douglas
Taggart, Laurence
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  surname: Paterson
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  organization: NHS Ayrshire & Arran
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intellectual disability
posttraumatic stress disorder
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Snippet Objective To report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC)...
To report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone...
ObjectiveTo report the results of the first randomized feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus...
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pubmed
crossref
wiley
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 806
SubjectTerms Adult
Clinical trials
Desensitization
Desensitization (Psychology)
Diagnostic and Statistical Manual of Mental Disorders
Evidence-based medicine
eye movement desensitization and reprocessing
Eye Movement Desensitization Reprocessing - methods
Eye movements
Feasibility Studies
Female
Follow-Up Studies
Humans
Intellectual disabilities
Intellectual Disability
Male
Middle Aged
Mixed methods research
Motor Reactions
Outcome Assessment, Health Care
Post traumatic stress disorder
Posttraumatic Stress Disorder
Psychotherapy
Qualitative Research
randomized feasibility study
Single-Blind Method
Stress Disorders, Post-Traumatic - therapy
Title A mixed‐methods, randomized controlled feasibility trial of Eye Movement Desensitization and Reprocessing (EMDR) plus Standard Care (SC) versus SC alone for DSM‐5 Posttraumatic Stress Disorder (PTSD) in adults with intellectual disabilities
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjar.12570
https://www.ncbi.nlm.nih.gov/pubmed/30714684
https://www.proquest.com/docview/2233736059
https://www.proquest.com/docview/2179484790
Volume 32
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