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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04551508
Other study ID # 31-1521-440 (STPS)
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 9, 2020
Est. completion date November 1, 2021

Study information

Verified date March 2022
Source Hospitalsenheden Vest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Observational study comparing three different methods of delirium detection in critically ill patients.


Description:

The DELIS-3 study aims to compare three different approaches to detection of ICU (intensive care unit) delirium in critically ill patients. The CAM-ICU (Confusion Assessment Method for the ICU) and the ICDSC (Intensive Care Delirium Screening Checklist) have both been developed in the early 1990. The CAM-ICU is either positive or negative, whereas the ICDSC is a score between 0-8. A score above 3 is delirium positive. Neither scale has been validated as severity scales. The novel CAM-ICU-7 is developed from the original CAM-ICU and has been validated as a severity scale. Detection of delirium in critically ill patients is highly necessary as delirium can be very painful to the patient. Moreover, certain subtypes of delirium is associated with increased mortality and poorer cognitive outcome when patients are followed up on long term. Therefore, delirium screening of all patients is standard care in most intensive care units. However, there is also a need to assess severity of delirium. The recently published CAM-ICU-7 has now been translated to Danish and this study will explore its performance compared to the CAM-ICU and the ICDSC. In 17 Danish ICU's 10 nurses will be trained in using all three instruments. Each nurse will subsequently screen 10 patients each with all three instruments as part of their normal practice. The sequence of the instruments will be randomized to avoid that one instrument is favored by always being used first, second or last. For each patient the following data will be collected: sex, age, reason for hospitalization (medical, neurological, surgical/ acute, planned), ventilator treatment, ability to verbalize, RASS score (sedation and agitation score) severity of disease (SMS score) and time of admission. After all screenings has been collected, nurses will fill in a questionnaire on their perceptions of each scales' ability to reliably detect delirium, userfriendliness and how time consuming each scale were to use.


Recruitment information / eligibility

Status Completed
Enrollment 1126
Est. completion date November 1, 2021
Est. primary completion date November 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - All patients admitted to critical care units. Exclusion Criteria: - Patients with RASS score of -3, -4, -5

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Aalborg Universitetshospital Aalborg
Denmark Aarhus Universitetshospital Aarhus
Denmark Rigshospitalet Copenhagen Ø
Denmark Sydvestjysk sygehus Esbjerg
Denmark Regionshospitalet Herning Herning Region Midtjylland
Denmark Nordsjællands Hospital Hillerød
Denmark Holbæk Sygehus Holbæk
Denmark Regionshospitalet Holstebro Holstebro Region Midtjylland
Denmark Regionshospitalet Horsens Horsens
Denmark Sjællands Universitetshospital Køge
Denmark Odense Universitetshospital Odense C
Denmark Regionshospitalet Randers Randers
Denmark Vejle Sygehus Vejle
Denmark Regionshospitalet Viborg Viborg

Sponsors (1)

Lead Sponsor Collaborator
Hospitalsenheden Vest

Country where clinical trial is conducted

Denmark, 

References & Publications (5)

Almgren M, Lundmark M, Samuelson K. The Richmond Agitation-Sedation Scale: translation and reliability testing in a Swedish intensive care unit. Acta Anaesthesiol Scand. 2010 Jul;54(6):729-35. doi: 10.1111/j.1399-6576.2009.02173.x. Epub 2009 Dec 5. — View Citation

Bergeron N, Dubois MJ, Dumont M, Dial S, Skrobik Y. Intensive Care Delirium Screening Checklist: evaluation of a new screening tool. Intensive Care Med. 2001 May;27(5):859-64. — View Citation

Ely EW, Margolin R, Francis J, May L, Truman B, Dittus R, Speroff T, Gautam S, Bernard GR, Inouye SK. Evaluation of delirium in critically ill patients: validation of the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU). Crit Care Med. 2001 Jul;29(7):1370-9. — View Citation

Granholm A, Perner A, Krag M, Marker S, Hjortrup PB, Haase N, Holst LB, Collet MO, Jensen AKG, Møller MH. External validation of the Simplified Mortality Score for the Intensive Care Unit (SMS-ICU). Acta Anaesthesiol Scand. 2019 Oct;63(9):1216-1224. doi: 10.1111/aas.13422. Epub 2019 Jul 4. — View Citation

Khan BA, Perkins AJ, Gao S, Hui SL, Campbell NL, Farber MO, Chlan LL, Boustani MA. The Confusion Assessment Method for the ICU-7 Delirium Severity Scale: A Novel Delirium Severity Instrument for Use in the ICU. Crit Care Med. 2017 May;45(5):851-857. doi: 10.1097/CCM.0000000000002368. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Confusion Assessment Method of the Intensive Care Unit (CAM-ICU) Clinical test for detecting delirium bedside, can be used by non-psychiatrists. CAM-ICU can be either positive (indicating delirium) or negative. Day 1
Primary Confusion assessment method of the intensive care unit 7 (CAM-ICU -7) Clinical test for detecting delirium bedside, can be used by non-psychiatrists. CAM-ICU-7 can yield a score of 0-7 points, higher values indicative of worse delirium. Day 1
Primary intensive care delirium screening checklist (ICDSC) Clinical test for detecting delirium bedside, can be used by non-psychiatrists. ICDSC can yield a score of 0-8 points, higher values indicative of worse delirium. Day 1
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