The objective is to examine the feasibility of performing EMDR in physical trauma patients with symptoms of ASD. This provides information insight the possibility of doing a psychological EMDR intervention in the clinical hospital setting.
ID
Bron
Aandoening
acute stress disorder
trauma
injury
feasibility study
Acute stress stoornis
Trauma
Lichamelijk trauma
Ongeval
Haalbaarheid onderzoek
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Presence and severity of ASD symptoms
Achtergrond van het onderzoek
The inclusion period will be 12 months. Participants will be screened for ASD symptoms. Patients with symptoms of ASD will be asked to participate and to undergo EMDR treatment. After signing the informed consent form (IC), patients will be asked to complete questionnaires at three time points. First, to complete socio-demographic information and ASD questionnaires at baseline. Other measurements of ASD are directly after finishing the EMDR intervention and one month later. EMDR treatment will be offered as soon as possible after patients’ confirmation for participation (i.e., signing IC). Clinical information will be abstracted from patients’ medical records. Based on a sample size calculation (independent sample t-test), 52 patients with symptoms of ASD will receive the EMDR intervention.
Doel van het onderzoek
The objective is to examine the feasibility of performing EMDR in physical trauma patients with symptoms of ASD. This provides information insight the possibility of doing a psychological EMDR intervention in the clinical hospital setting.
Onderzoeksopzet
Directly after signing the informed consent form, then directly after ending the EMDR intervention and one month after completing the intervention.
Onderzoeksproduct en/of interventie
This intervention consists of one up to three EMDR sessions, with a duration of 45 minutes, focused on the source of ASD symptoms. This intervention will be performed by psychologists, who are also EMDR practitioners and specialized in treating physical trauma patients.
Algemeen / deelnemers
Eva Visser
P.O. Box 90151
Tilburg 5000 LC
The Netherlands
013-221 0000
e.visser@etz.nl
Wetenschappers
Eva Visser
P.O. Box 90151
Tilburg 5000 LC
The Netherlands
013-221 0000
e.visser@etz.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
being treated in the shock room
aged 18 or older
presence of ASD symptoms (based on the DSM-5 criteria).
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
severe traumatic brain injury (i.e., Glasgow Coma Score ¡Ü 8)
dementia
insufficient knowledge of the Dutch language (verbal and writing)
Opzet
Deelname
Voornemen beschikbaar stellen Individuele Patiënten Data (IPD)
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Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
Register | ID |
---|---|
NTR-new | NL6437 |
NTR-old | NTR7228 |
CCMO | NL66194.028.18 |
OMON | NL-OMON48566 |