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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06202729
Other study ID # MCLSEH1
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 8, 2023
Est. completion date December 11, 2023

Study information

Verified date March 2024
Source Medical Centre Leeuwarden
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the present study is to determine the prevalence of anxiety in adult patients attending the ED of the Medical Centre Leeuwarden.


Description:

Determination of the prevalence of anxiety in adult patients attending the ED of the Medical Centre Leeuwarden. Secondarily, the common causes of anxiety and the effect of anxiety on the time of presentation to the ED and perceived pain will be investigated. In addition to gaining more insight into the relationship between the ED and anxiety, the study aims to raise awareness of anxiety among patients in the ED.


Recruitment information / eligibility

Status Completed
Enrollment 139
Est. completion date December 11, 2023
Est. primary completion date December 11, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Age 18 years and older - Competent to decide on study participation - Written informed consent obtained Exclusion Criteria: - Patients from who a Dutch questionnaire cannot be obtained (e.g. delirious, comatose, confused and non-Dutch speaking patients) - If the reason for ED presentation is: suicide, intoxication or reporting from a sexual violence center - Patients with an active eating disorder - Patient already included in this study - Objection to the use of patient data registered in the EPD

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Questionnaire
GAD-7, VAS-A, NRS

Locations

Country Name City State
Netherlands MCLeeuwarden Leeuwarden Friesland

Sponsors (1)

Lead Sponsor Collaborator
Medical Centre Leeuwarden

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Prevalence of anxiety measured by GAD-7 and VAS-A What is the prevalence of anxiety among adult patients in the ED? Two weeks prior to ED presentation
Secondary Timing ER visit What influence does fear have on the timing of the ER visit? 1 Day
Secondary Start of fear (open question) What was the moment when fear arised? 1 Day
Secondary Influence of pain (NRS) on fear (GAD-7) What is the influence of pain on fear experienced? 1 Day
Secondary Cause of fear (open question) What is the cause of fear? 1 Day
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