A follow-up clinic for intensive care units (ICU) survivors reduces the incidence of post traumatic stress disorder (PTSD) after 1 year of follow-up.
ID
Bron
Aandoening
post traumatic stress disorder, PTSD
posttraumatische stressstoornis, PTSS
quality of life
kwaliteit van leven
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Incidence of PTSD at one year follow-up.
Achtergrond van het onderzoek
Rationale:
Gradually more Intensive Care Units (ICUs) provide a follow-up clinic for ICU survivors, but it is unclear whether these clinics contribute to better long-term outcomes.
Objective:
To evaluate the effectiveness of a follow-up clinic for ICU survivors on their risk of post traumatic stress disorder (PTSD) and health related quality of life, 12 months after admission to a mixed level 3 intensive care unit.
Study design:
Cluster randomised controlled trial (stepped wedge design).
Study population:
Patients admitted for more than 48 hours to the ICU of the University Medical Center Utrecht.
Intervention: Follow-up clinic for ICU survivors, two months after ICU discharge with possible referral and treatment of PTSD by a psychiatrist.
Main study parameters/endpoints:
PTSD assessed with the Impact of Events questionnaire.
Secondary endpoints: Quality of life, cognitive impairment, impairment in daily activities, (other) anxiety disorders, depression.
Doel van het onderzoek
A follow-up clinic for intensive care units (ICU) survivors reduces the incidence of post traumatic stress disorder (PTSD) after 1 year of follow-up.
Onderzoeksopzet
1. Baseline questionnaire for family;
2. Questionnaire 1 month after ICU discharge;
3. Primary and secondary outcomes: Questionnaire 1 year after ICU discharge.
Onderzoeksproduct en/of interventie
Visit to a follow-up clinic 2 months after ICU discharge.
Patients will recieve 1 month after discharge (= 1 month prior to their visit) a questionnaire with the Hospital Anxiety and Depression Scale (HADS), the Impact of Event Scale (IES) and the Cognitive FailuresQuestionnaire (CFQ).
Patients who score 12 or more on the HADS, above 27 on the IES and/or above 40 on the CFQ are offered a referral for thorough diagnostics and treatment if neccesary.
Moreover, the intensivist can offer referral to other specialisms, e.g. to an otolaryngologist if he believes it could benefit the patient.
Publiek
Department of Anaesthesiology and Intensive Care<br>
Mail Stop F.06.149<br>
PO Box 85500
Diederick Dijk, van
Utrecht 3508 GA
The Netherlands
+31 (0)88 7561136
d.vandijk@umcutrecht.nl
Wetenschappelijk
Department of Anaesthesiology and Intensive Care<br>
Mail Stop F.06.149<br>
PO Box 85500
Diederick Dijk, van
Utrecht 3508 GA
The Netherlands
+31 (0)88 7561136
d.vandijk@umcutrecht.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
ICU stay longer than 48 hours.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Mortality during treatment or 2 months after ICU discharge;
2. ICU admission with an indication primarily for neurology/neurosurgery;
3. Patients less than 18 years;
4. Patients (or authorised relatives) who do not consent to participate.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
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In overige registers
Register | ID |
---|---|
NTR-new | NL3557 |
NTR-old | NTR3716 |
Ander register | METC of UMC Utrecht : 12-418/C |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |