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Clinical Trials/NCT04841122
NCT04841122
Terminated
Not Applicable

Improved Patient Safety for Acute Restless Medical Patients With Supplemental Observation

Aalborg University Hospital1 site in 1 country8 target enrollmentApril 19, 2021
ConditionsDelirium

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Delirium
Sponsor
Aalborg University Hospital
Enrollment
8
Locations
1
Primary Endpoint
Change in Confusion Assessment Score
Status
Terminated
Last Updated
4 years ago

Overview

Brief Summary

The aim of the study is to investigate whether supplemental camera observation directly linked to the nurse's phone will improve patient safety for acute medical care patients', who are restless, confused or in risk of development of acute delirium. The setting is an acute medical care ward.

The expected result is a reduced incidence of patients with delirious condition, patients who fall or unintentionally remove intravenous access or catheters. Thus, higher patient safety and more efficient patient trajectories are expected, as well as a reduced need for treatment, care and rehabilitation after discharge.

Registry
clinicaltrials.gov
Start Date
April 19, 2021
End Date
September 30, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mette Geil Kollerup

Principal investigator and postdoc.

Aalborg University Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients over 65 years of age with a CAM score of 2 or higher.

Exclusion Criteria

  • severe dementia
  • need for permanent guard

Outcomes

Primary Outcomes

Change in Confusion Assessment Score

Time Frame: First measurement at admission and second measurement within 24 hours.

Assessed by Confusion Assessment Method (CAM) screening tool. Minimum value is 0, Maximum value is 4. Higher score means higher risk of developing Delirium.

Secondary Outcomes

  • Number of patient falls(The time the patient is assessed during the observation period.)
  • Number of administrations of sedatives(The time the patient is assessed during the observation period.)
  • Discontinuation of accesses(The time the patient is assessed during the observation period.)

Study Sites (1)

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