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The Impact of Nursing Delirium Preventive Interventions in the Intensive Care Unit (UNDERPIN-ICU)

Primary Purpose

Delirium

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
UNDERPIN-ICU program
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Delirium focused on measuring Prevention, Critical care, Delirium, Nurse, RCT

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • aged ≥ 18 years
  • surgical, medical or trauma patients
  • admitted to one of the participating ICUs
  • at high risk for delirium (>35% determined with the E-PRE-DELIRIC prediction tool)

Exclusion Criteria:

  • delirious before ICU admission
  • an ICU stay < one day
  • reliable assessment for delirium is not possible due to: sustained coma; serious auditory or visual disorders; inability to understand Dutch; severely mentally disabled; serious receptive aphasia.

Sites / Locations

  • Radboud University Medical Center
  • Haaglanden Medical Center location Westeinde
  • Hospital Gelderse Vallei
  • Medical Spectrum Twente
  • Hospital St. Jansdal
  • Medical Center Leeuwarden
  • Hospital ETZ location Elisabeth
  • Hospital ETZ location Tweesteden
  • Bernhoven Hospital
  • Maxima Medical Center
  • ISALA clinics

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Active Comparator

Arm Label

Control - standard care

Intervention group

Arm Description

Prior to implementation of the intervention package the current standard of care will be maintained.

After implementation the intervention package will be implemented as standard care.

Outcomes

Primary Outcome Measures

The number of delirium-coma-free days
The number of days a patient is not delirious and not in coma in 28 days starting from the day of inclusion in the study after ICU admission.

Secondary Outcome Measures

Delirium incidence
One or more episodes of positive delirium screening after ICU admission.
The number of days of survival
The number of days survived since ICU admission.
The number of days of survival
The number of days survived since ICU admission.
Duration of mechanical ventilation
The number of days a patient was mechanically ventilated.
Incidence of re-intubation
Patients who need to be intubated within 28 days after ICU admission, following a previous extubation, irrespectively the reason for re-intubation, will be counted as incident case for re-intubation.
Incidence of ICU re-admission
Patients who need to be readmitted to the ICU within 28 days, irrespectively the reason for readmission, will be counted as incident cases for ICU readmission.
Incidence of unplanned removal of tubes/catheters
Incidents in which patients remove their tube or catheter themselves will be counted as incident cases for unplanned removal. The period in which this is measured is during patients' ICU stay or during the period when the patient is delirious (in case a patient is discharged to the ward) with a maximum of 28 days.
Incidence of physical restraints
Patients who need physical restraints (fixation of their limbs to prevent them from removing tubes or lines) within 28 days, will be counted as incident cases for physical restraints.
ICU length of stay
This is defined as the number of days a patient is admitted to the ICU. Hospital length of stay is defined as number of days a patient is admitted to the hospital.
Hospital length of stay
This is defined as the number of days a patient is admitted to the ICU. Hospital length of stay is defined as number of days a patient is admitted to the hospital.
Health related quality of Life (HRQoL)
Health related quality of Life (HRQoL)
Post-hoc analysis
Cost-effectiveness

Full Information

First Posted
November 25, 2016
Last Updated
October 8, 2020
Sponsor
Radboud University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development
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1. Study Identification

Unique Protocol Identification Number
NCT03002701
Brief Title
The Impact of Nursing Delirium Preventive Interventions in the Intensive Care Unit
Acronym
UNDERPIN-ICU
Official Title
The Impact of nUrsiNg DEliRium Preventive INterventions in the Intensive Care Unit (UNDERPIN-ICU): A Multi-centre, Stepped Wedge Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
December 31, 2016 (Actual)
Primary Completion Date
May 31, 2019 (Actual)
Study Completion Date
May 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Radboud University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Delirium is a common disorder in Intensive Care Unit (ICU) patients and is associated with serious short- and long-term consequences. This study focuses on a program of standardized nursing and physical therapy interventions to prevent delirium in the ICU, and determines the effect of the program on the number of delirium-coma-free days in 28 days and several secondary outcomes in a multicenter randomized controlled trial.
Detailed Description
Delirium is a common disorder in Intensive Care Unit (ICU) patients and is associated with serious short- and long-term consequences, including re-intubations, ICU readmissions, prolonged ICU and hospital stay, persistent cognitive problems, and higher mortality rates. Considering the high incidence of delirium and its consequences, prevention of delirium is imperative. This study focuses on a program of standardized nursing and physical therapy interventions to prevent delirium in the ICU, called UNDERPIN-ICU (nUrsiNg DEliRium Preventive INterventions in the ICU). Objective: To determine the effect of the UNDERPIN-ICU program on the number of delirium-coma-free days in 28 days and several secondary outcomes, such as delirium incidence, the number of days of survival in 28 and 90 days and delirium-related outcomes. Design and Setting: A multicenter stepped wedge cluster randomized controlled trial. Methods: Eight to ten Dutch ICUs will implement the UNDERPIN-ICU program in a randomized order. Every two months the UNDERPIN-ICU program will be implemented in an additional ICU following a two months period of staff training. UNDERPIN-ICU consists of standardized protocols focusing on several modifiable risk factors for delirium, including cognitive impairment, sleep deprivation, immobility and visual and hearing impairment. Participants: ICU patients aged ≥ 18 years (surgical, medical, or trauma) and at high risk for delirium, E-PRE-DELIRIC ≥35%, will be included, unless delirium was detected prior ICU admission, expected length of ICU stay is less then one day or when delirium assessment is not possible.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Delirium
Keywords
Prevention, Critical care, Delirium, Nurse, RCT

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1750 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control - standard care
Arm Type
No Intervention
Arm Description
Prior to implementation of the intervention package the current standard of care will be maintained.
Arm Title
Intervention group
Arm Type
Active Comparator
Arm Description
After implementation the intervention package will be implemented as standard care.
Intervention Type
Behavioral
Intervention Name(s)
UNDERPIN-ICU program
Intervention Description
UNDERPIN-ICU consists of standardized protocols focusing on several modifiable risk factors for delirium, including cognitive impairment, sleep deprivation, immobility and visual and hearing impairment.
Primary Outcome Measure Information:
Title
The number of delirium-coma-free days
Description
The number of days a patient is not delirious and not in coma in 28 days starting from the day of inclusion in the study after ICU admission.
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Delirium incidence
Description
One or more episodes of positive delirium screening after ICU admission.
Time Frame
28 days
Title
The number of days of survival
Description
The number of days survived since ICU admission.
Time Frame
28 days
Title
The number of days of survival
Description
The number of days survived since ICU admission.
Time Frame
90 days
Title
Duration of mechanical ventilation
Description
The number of days a patient was mechanically ventilated.
Time Frame
28 days
Title
Incidence of re-intubation
Description
Patients who need to be intubated within 28 days after ICU admission, following a previous extubation, irrespectively the reason for re-intubation, will be counted as incident case for re-intubation.
Time Frame
28 days
Title
Incidence of ICU re-admission
Description
Patients who need to be readmitted to the ICU within 28 days, irrespectively the reason for readmission, will be counted as incident cases for ICU readmission.
Time Frame
28 days
Title
Incidence of unplanned removal of tubes/catheters
Description
Incidents in which patients remove their tube or catheter themselves will be counted as incident cases for unplanned removal. The period in which this is measured is during patients' ICU stay or during the period when the patient is delirious (in case a patient is discharged to the ward) with a maximum of 28 days.
Time Frame
28 days
Title
Incidence of physical restraints
Description
Patients who need physical restraints (fixation of their limbs to prevent them from removing tubes or lines) within 28 days, will be counted as incident cases for physical restraints.
Time Frame
28 days
Title
ICU length of stay
Description
This is defined as the number of days a patient is admitted to the ICU. Hospital length of stay is defined as number of days a patient is admitted to the hospital.
Time Frame
365 days
Title
Hospital length of stay
Description
This is defined as the number of days a patient is admitted to the ICU. Hospital length of stay is defined as number of days a patient is admitted to the hospital.
Time Frame
365 days
Title
Health related quality of Life (HRQoL)
Time Frame
90 days after ICU admission
Title
Health related quality of Life (HRQoL)
Time Frame
365 days after ICU admission
Title
Post-hoc analysis
Time Frame
During admission
Title
Cost-effectiveness
Time Frame
During ICU admission

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: aged ≥ 18 years surgical, medical or trauma patients admitted to one of the participating ICUs at high risk for delirium (>35% determined with the E-PRE-DELIRIC prediction tool) Exclusion Criteria: delirious before ICU admission an ICU stay < one day reliable assessment for delirium is not possible due to: sustained coma; serious auditory or visual disorders; inability to understand Dutch; severely mentally disabled; serious receptive aphasia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark van den Boogaard, PhD
Organizational Affiliation
Radboud University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud University Medical Center
City
Nijmegen
State/Province
Gelderland
ZIP/Postal Code
6500HB
Country
Netherlands
Facility Name
Haaglanden Medical Center location Westeinde
City
Den Haag
Country
Netherlands
Facility Name
Hospital Gelderse Vallei
City
Ede
Country
Netherlands
Facility Name
Medical Spectrum Twente
City
Enschede
Country
Netherlands
Facility Name
Hospital St. Jansdal
City
Harderwijk
Country
Netherlands
Facility Name
Medical Center Leeuwarden
City
Leeuwarden
Country
Netherlands
Facility Name
Hospital ETZ location Elisabeth
City
Tilburg
Country
Netherlands
Facility Name
Hospital ETZ location Tweesteden
City
Tilburg
Country
Netherlands
Facility Name
Bernhoven Hospital
City
Uden
Country
Netherlands
Facility Name
Maxima Medical Center
City
Veldhoven
Country
Netherlands
Facility Name
ISALA clinics
City
Zwolle
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
28013104
Citation
Wassenaar A, Rood P, Schoonhoven L, Teerenstra S, Zegers M, Pickkers P, van den Boogaard M. The impact of nUrsiNg DEliRium Preventive INnterventions in the Intensive Care Unit (UNDERPIN-ICU): A study protocol for a multi-centre, stepped wedge randomized controlled trial. Int J Nurs Stud. 2017 Mar;68:1-8. doi: 10.1016/j.ijnurstu.2016.11.018. Epub 2016 Dec 8.
Results Reference
result
PubMed Identifier
34170798
Citation
Rood PJT, Zegers M, Ramnarain D, Koopmans M, Klarenbeek T, Ewalds E, van der Steen MS, Oldenbeuving AW, Kuiper MA, Teerenstra S, Adang E, van Loon LM, Wassenaar A, Vermeulen H, Pickkers P, van den Boogaard M; UNDERPIN-ICU Study Investigators. The Impact of Nursing Delirium Preventive Interventions in the ICU: A Multicenter Cluster-randomized Controlled Clinical Trial. Am J Respir Crit Care Med. 2021 Sep 15;204(6):682-691. doi: 10.1164/rccm.202101-0082OC.
Results Reference
derived
Links:
URL
http://dx.doi.org/10.1016/j.ijnurstu.2016.11.018
Description
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The Impact of Nursing Delirium Preventive Interventions in the Intensive Care Unit

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