Trauma-focused EMDR for Personality disorders among Outpatients (TEMPO): study protocol for a multi-centre, single-blind, randomized controlled trial

被引:10
|
作者
Hofman, Simon [1 ]
Hafkemeijer, Laurian [2 ]
de Jongh, Ad [3 ,4 ,5 ,6 ,7 ,8 ]
Starrenburg, Annemieke [2 ]
Slotema, Karin [1 ,9 ]
机构
[1] Parnassia Psychiat Inst, Dept Personal Disorders, Lijnbaan 4, NL-2512 VA The Hague, Netherlands
[2] GGZ Delfland, Dept Adult Psychiat, Delft, Netherlands
[3] Univ Amsterdam, Acad Ctr Dent Amsterdam ACTA, Amsterdam, Netherlands
[4] Vrije Univ Amsterdam, Amsterdam, Netherlands
[5] PSYTREC, Res Dept, Bilthoven, Netherlands
[6] Salford Univ, Sch Hlth Sci, Manchester, Lancs, England
[7] Univ Worcester, Inst Hlth & Soc, Worcester, England
[8] Queens Univ Belfast, Sch Psychol, Belfast, Antrim, North Ireland
[9] Erasmus Univ, Dept Psychol Educ & Child Studies, Rotterdam, Netherlands
关键词
EMDR; Personality disorder; Trauma; Effectiveness; Cost-effectiveness; Economic evaluation; Predictors; Treatment experiences; Study protocol; Randomized controlled trial; POSTTRAUMATIC-STRESS-DISORDER; STRUCTURED CLINICAL INTERVIEW; QUALITY-OF-LIFE; AXIS-II; PSYCHOMETRIC PROPERTIES; INTERRATER RELIABILITY; MENTAL-DISORDERS; BORDERLINE; ADOLESCENCE; THERAPY;
D O I
10.1186/s13063-022-06082-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Existing recommended treatment options for personality disorders (PDs) are extensive and costly. There is emerging evidence indicating that trauma-focused treatment using eye movement desensitization and reprocessing (EMDR) therapy aimed at resolving memories of individuals' adverse events can be beneficial for this target group within a relatively short time frame. The primary purpose of the present study is to determine the effectiveness of EMDR therapy versus waiting list in reducing PD symptom severity. Furthermore, the effects of EMDR therapy on trauma symptom severity, loss of diagnosis, personal functioning, quality of life, and mental health outcomes will be determined. In addition, the cost-effectiveness of EMDR therapy in the treatment of PDs is investigated. Moreover, predictors of treatment success, symptom deterioration and treatment discontinuation will be assessed. Lastly, experiences with EMDR therapy will be explored. Method: In total, 159 patients with a PD will be included in a large multicentre single-blind randomized controlled trial. The Structured Clinical Interview for DSM-5 Personality Disorders will be used to determine the presence of a PD. Participants will be allocated to either a treatment condition with EMDR therapy (ten biweekly 90-min sessions) or a waiting list Three months after potential treatment with EMDR therapy, patients can receive treatment as usual for their PD. All participants are subject to single-blinded baseline, post-intervention and 3-, 6- and 12-month follow-up assessments. The primary outcome measures are the Assessment of DSM-IV Personality Disorders and the Clinician-Administered PTSD Scale for DSM-5. For cost-effectiveness, the Treatment Inventory of Costs in Patients with psychiatric disorders, EuroQol-5D-3L, and the Mental Health Quality of Life Questionnaire will be administered. The PTSD Checklist for DSM-5, Brief State Paranoia Checklist and Difficulties in Emotion Regulation Scale will be used to further index trauma symptom severity. Type of trauma is identified at baseline with the Childhood Trauma Questionnaire-SF and Life Events Checklist for the DSM-5. Personal functioning and health outcome are assessed with the Level of Personality Functioning Scale-BF 2.0, Outcome Questionnaire-45 and Mental Health Quality of Life Questionnaire. Experiences with EMDR therapy of patients in the EMDR therapy condition are explored with a semi-structured interview at post-intervention. Discussion: It is expected that the results of this study will contribute to knowledge about the effectiveness, and cost-effectiveness of trauma-focused treatment using EMDR therapy in individuals diagnosed with a PD. Follow-up data provide documentation of long-term effects of EMDR therapy on various outcome variables, most importantly the reduction of PD symptom severity and loss of diagnoses.
引用
收藏
页数:15
相关论文
共 50 条
  • [41] Effect of electroacupuncture versus solifenacin for moderate and severe overactive bladder: a multi-centre, randomized controlled trial study protocol
    Wen, Qian
    Li, Ning
    Wang, Xueling
    Li, Hao
    Tian, Fengwei
    Chen, Weiwei
    Lu, Yanyan
    Liu, Zhishun
    BMC COMPLEMENTARY MEDICINE AND THERAPIES, 2020, 20 (01) : 224
  • [42] Whole body vibration exercise for chronic low back pain: study protocol for a single-blind randomized controlled trial
    Wang, Xue-Qiang
    Pi, Yan-Lin
    Chen, Pei-Jie
    Chen, Bin-Lin
    Liang, Lei-Chao
    Li, Xin
    Wang, Xiao
    Zhang, Juan
    TRIALS, 2014, 15
  • [43] The effectiveness of a trauma-focused psycho-educational secondary prevention program for children exposed to interparental violence: study protocol for a randomized controlled trial
    Overbeek, Mathilde M.
    de Schipper, J. Clasien
    Lamers-Winkelman, Francien
    Schuengel, Carlo
    TRIALS, 2012, 13
  • [44] The effects of parental components in a trauma-focused cognitive behavioral based therapy for children exposed to interparental violence: study protocol for a randomized controlled trial
    Visser, Margreet M.
    Telman, Machteld D.
    de Schipper, J. Clasien
    Lamers-Winkelman, Francien
    Schuengel, Carlo
    Finkenauer, Catrin
    BMC PSYCHIATRY, 2015, 15
  • [45] The effects of parental components in a trauma-focused cognitive behavioral based therapy for children exposed to interparental violence: study protocol for a randomized controlled trial
    Margreet M. Visser
    Machteld D. Telman
    J. Clasien de Schipper
    Francien Lamers-Winkelman
    Carlo Schuengel
    Catrin Finkenauer
    BMC Psychiatry, 15
  • [46] The effectiveness of a trauma-focused psycho-educational secondary prevention program for children exposed to interparental violence: study protocol for a randomized controlled trial
    Mathilde M Overbeek
    J Clasien de Schipper
    Francien Lamers-Winkelman
    Carlo Schuengel
    Trials, 13
  • [47] Mesh Or Patch for Hernia on Epigastric and Umbilical Sites (MORPHEUS trial): study protocol for a multi-centre patient blinded randomized controlled trial
    Ponten, Jeroen E. H.
    Leenders, Bart J. M.
    Charbon, Jan A.
    Lettinga-van de Poll, Tanja
    Heemskerk, Jeroen
    Martijnse, Ingrid S.
    Konsten, Joop L. M.
    Nienhuijs, Simon W.
    BMC SURGERY, 2014, 14
  • [48] Mesh Or Patch for Hernia on Epigastric and Umbilical Sites (MORPHEUS trial): study protocol for a multi-centre patient blinded randomized controlled trial
    Jeroen EH Ponten
    Bart JM Leenders
    Jan A Charbon
    Tanja Lettinga - van de Poll
    Jeroen Heemskerk
    Ingrid S Martijnse
    Joop LM Konsten
    Simon W Nienhuijs
    BMC Surgery, 14
  • [49] A multi-centre, randomised controlled trial of the effectiveness of PDSAFE to prevent falls among people with Parkinson’s: study protocol
    Victoria A Goodwin
    Ruth Pickering
    Claire Ballinger
    Helen Roberts
    Emma McIntosh
    Sarah Lamb
    Alice Nieuwboer
    Lynn Rochester
    Ann Ashburn
    BMC Neurology, 15
  • [50] A multi-centre, randomised controlled trial of the effectiveness of PDSAFE to prevent falls among people with Parkinson's: study protocol
    Goodwin, Victoria A.
    Pickering, Ruth
    Ballinger, Claire
    Roberts, Helen
    McIntosh, Emma
    Lamb, Sarah
    Nieuwboer, Alice
    Rochester, Lynn
    Ashburn, Ann
    BMC NEUROLOGY, 2015, 15