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Status unknownNCT01847742Updated Aug 9, 2013

EMDR Intervention for Psychological Trauma Among Syrian Refugees

An interventional study of Eye Movement Desensitization and Reprocessing Therapy in Psychological Trauma, sponsored by Istanbul Sehir University. Status unknown at 1 site in Turkey. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2013-08-09.

Sponsored by Istanbul Sehir University · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Aug 2013), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
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Study summary

To implement an EMDR (Eye Movement Desensitization and Reprocessing)intervention to treat the trauma symptoms among Syrian Refugees.

Read the detailed description

In this project we aim to treat the posttraumatic stress disorder (PTSD) symptoms among Syrian refugees through an effective psycho-therapy technique called Eye Movement Desensitization and Reprocessing (EMDR). Randomly selected refugees will be assessed through MINI PLUS for the diagnose of PTSD. Eighty refugees with PTSD will be randomly allocated to either 7 sessions EMDR or wait-list control group.Symptoms of PTSD (MINI PLUS, HTQ, IES-R) and depression and anxiety (BDI, HSCL)will be assessed at pre- and post-treatment and 4 weeks follow-up.

However, to our knowledge this is one of the first intervention studies which will be conducted in a refugee camp. Therefore we expect to have some practical and logical problems. In order to see the feasibility and efficacy of EMDR among Syrian refugees, before the main study we aim to run a pilot study with less participants. In the pilot we will assess the posttraumatic stress symptoms with Impact of Event Scale-Revised (IES-R) and the depressive symptoms through Beck Depression Inventory (BDI-II).

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Conditions studied

  • Psychological Trauma
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In context

Wounds and Injuries

5,056 studies on the registry are indexed under Wounds and Injuries; 861 are open to participants now.

This study's planned enrollment of 80 is above the median of 52 across 3,239 interventional studies indexed under Wounds and Injuries.

Browse Wounds and Injuries studies →

Lead sponsor

Istanbul Sehir University is the lead sponsor of 4 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • trauma symptoms

Exclusion criteria

Exclusion Criteria:

  • pregnancy
  • current or past psychotic disorder
  • current or past substance abuse or dependence
  • serious physical illness
  • active suicidal ideation
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    EMDR intervention

    40 participants with trauma symptoms will be randomly assigned to treatment group and receive EMDR intervention for trauma symptoms.EMDR is a trauma focused therapy starts with resource development and continue with bilateral stimulation while working on the most troubling traumatic memory.

    Behavioral: Eye Movement Desensitization and Reprocessing Therapy

  • No intervention
    Waiting List

    40 participants with trauma symptoms will be randomly assigned to waiting list as the control group.

Interventions

  • BehavioralEye Movement Desensitization and Reprocessing Therapy
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What researchers measure

Primary outcomes

  1. score on Harvard Trauma Questionnaire (at the main study)

    The change in HTQ score will be assessed after the EMDR treatment has finished after 7 weeks(estimated).

    Time frame: before and after the treatment,an expected average of 7 weeks of EMDR treatment

  2. Impact of Event Scale Revised (at the pilot study and the main study)

    The change in IES-R score will be assessed after the EMDR treatment has finished after 7 weeks(estimated).

    Time frame: pre- and post treatment

Secondary outcomes

  1. score on HSCL for depressive and anxiety symptoms (at the main study)

    The change in HSCL score will be assessed after the EMDR treatment has finished in 7 weeks in average.

    Time frame: before and after the treatment, an expected average of 7 weeks of EMDR treatment

  2. Score on BDI-II (pilot study and the main study)

    A change in BDI-II will be assessed after the EMDR treatment has completed in 7 weeks.

    Time frame: before and after EMDR treatment, an expected average of 7 weeks of EMDR treatment

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Study locations

1 of 1 sites recruiting
  • Kilis Camp for Refugees
    Gaziantep, Turkey
    Recruiting
08

References and documents

Publications

  • Acarturk C, Konuk E, Cetinkaya M, Senay I, Sijbrandij M, Gulen B, Cuijpers P. The efficacy of eye movement desensitization and reprocessing for post-traumatic stress disorder and depression among Syrian refugees: results of a randomized controlled trial. Psychol Med. 2016 Sep;46(12):2583-93. doi: 10.1017/S0033291716001070. Epub 2016 Jun 29. PubMed 27353367 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 9, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01847742
Lead sponsor
Istanbul Sehir University
Responsible party
Ceren Acarturk (Assistant Professor, Istanbul Sehir University) — Principal investigator
First posted
May 7, 2013
Start date
Apr 2013
Primary completion
Dec 2013 (estimated)
Completion
Feb 2014 (estimated)
Last update
Aug 9, 2013

Study contacts

Ceren Acarturk, PhD
Contact
cerenacarturk@sehir.edu.tr
0090216444 4034 ext. 9853

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2013. You cannot join it, but the record below documents what was studied.

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