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Effects of Feeding Schedule on the Development of ICU Delirium

Primary Purpose

ICU Delirium

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Enteric feeding
Sponsored by
Rutgers, The State University of New Jersey
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for ICU Delirium focused on measuring Mechanical ventilation, Tube feeds

Eligibility Criteria

21 Years - 89 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Admitted to the ICU
  • Mechanically ventilated
  • Receiving enteric feedings for at least 48 hours

Exclusion Criteria:

  • Pregnancy
  • Previously diagnosed neurocognitive disorders,
  • Alcohol withdrawal and history of alcohol dependence

Sites / Locations

  • Robert Wood Johnson Medical SchoolRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Continuous Feeding

Timed Feeding

Arm Description

Enteric feeding will be given continuously.

Enteric feeding will be given four times per day, approximating breakfast, lunch, a snack, and dinner.

Outcomes

Primary Outcome Measures

Percent of patients developing delirium.
The development of delirium as measured by the CAM-ICU (Confusion Assessment Method for the ICU) protocol. The percent of patients developing delirium will be assessed in each arm. Delirium will be assessed every 12 hours.

Secondary Outcome Measures

Change in sleep quality assessed using delta power.
Change in relative delta power on EEG will be assessed in each arm.
Change in sleep quality assessed using theta power.
Change in relative theta power on EEG will be assessed in each arm.
Change in sleep quality using beta power.
Change in relative beta power on EEG will be assessed in each arm.
Changes in circadian rhythm assessed using expression of PER2.
The difference between day and night expression of PER2 in serum will be compared between the two arms.
Changes in circadian rhythm assessed using expression of SIRT.
The difference between day and night expression of SIRT in serum will be compared between the two arms.
Changes in circadian rhythm assessed using cortisol.
The difference between day and night concentrations of serum free cortisol will be compared between the two arms.
Changes in circadian rhythm assessed using insulin.
The difference between day and night concentrations of serum insulin will be compared between the two arms.

Full Information

First Posted
April 23, 2021
Last Updated
June 29, 2022
Sponsor
Rutgers, The State University of New Jersey
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1. Study Identification

Unique Protocol Identification Number
NCT04870554
Brief Title
Effects of Feeding Schedule on the Development of ICU Delirium
Official Title
Effects of Feeding Schedule on the Development of ICU Delirium
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 26, 2021 (Actual)
Primary Completion Date
April 26, 2023 (Anticipated)
Study Completion Date
April 26, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rutgers, The State University of New Jersey

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will investigate if enteric feeding schedules alter the development of delirium in Intensive Care Unit patients who have been placed on mechanical ventilation. Delirium is an altered state of consciousness, which can involve agitation, inattention, and decreased awareness. We will enroll Intensive Care Unit patients who have been placed on a ventilator and are being given tube feedings. We will randomize participants into two groups: one group will receive continuous feedings via feeding tube, and the other group will receive feedings on a schedule to mimic breakfast, lunch, a snack, and dinner. Subjects will be assessed for the development of delirium. Subjects will also be monitored for sleep quality and biomarkers of circadian rhythm.
Detailed Description
Patients will need to have at least 48 hours of enteric feedings to be included, and will be stratified by their APACHE IV score. Patients will be randomized into time restricted feeding vs continuous feeding by investigators, with no change in caloric intake nor nutrient content from orders. Patients will be assessed for delirium using the CAM-ICU (Confusion Assessment Method in the Intensive Care Unit) screening tool every twelve hours. At the time of the CAM ICU assessment, as part of the experimental design, the patient's sleep will be monitored by X8 Sleep Profiler device, placed and secured to their forehead, and the Sleep Profiler device will collect information regarding sleep quality as assessed by relative delta power, relative theta power and relative beta power. For the circadian rhythm marker analysis, blood samples (15 mL) will be collected at two time points: a day sample will be collected between 6 and 7 AM and a night sample will be collected between 11 PM and 12 AM. Collection will start approximately 48 hours after ICU admission. The expressions of the genes PER2 and SIRT with their proteins will be analyzed. The samples will also be used to measure serum free cortisol and serum insulin levels.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
ICU Delirium
Keywords
Mechanical ventilation, Tube feeds

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients will be randomly assigned to one of two treatment groups: standard continuous feeding or timed feeding.
Masking
Participant
Masking Description
Participants will be under sedation. The outcome assessor for delirium (primary outcome) is not blinded. Assessors rating the sleep quality and biomarkers of circadian disruption (secondary outcomes) will be blinded.
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Continuous Feeding
Arm Type
No Intervention
Arm Description
Enteric feeding will be given continuously.
Arm Title
Timed Feeding
Arm Type
Experimental
Arm Description
Enteric feeding will be given four times per day, approximating breakfast, lunch, a snack, and dinner.
Intervention Type
Behavioral
Intervention Name(s)
Enteric feeding
Intervention Description
All subjects will be given nutrition enterally, corresponding to their calculated nutritional needs.
Primary Outcome Measure Information:
Title
Percent of patients developing delirium.
Description
The development of delirium as measured by the CAM-ICU (Confusion Assessment Method for the ICU) protocol. The percent of patients developing delirium will be assessed in each arm. Delirium will be assessed every 12 hours.
Time Frame
48 hours after admission to the ICU.
Secondary Outcome Measure Information:
Title
Change in sleep quality assessed using delta power.
Description
Change in relative delta power on EEG will be assessed in each arm.
Time Frame
Measurement will be made from study enrollment to extubation, up to 1 week.
Title
Change in sleep quality assessed using theta power.
Description
Change in relative theta power on EEG will be assessed in each arm.
Time Frame
Measurement will be made from study enrollment to extubation, up to 1 week.
Title
Change in sleep quality using beta power.
Description
Change in relative beta power on EEG will be assessed in each arm.
Time Frame
Measurement will be made from study enrollment to extubation, up to 1 week.
Title
Changes in circadian rhythm assessed using expression of PER2.
Description
The difference between day and night expression of PER2 in serum will be compared between the two arms.
Time Frame
48 hours after study enrollment.
Title
Changes in circadian rhythm assessed using expression of SIRT.
Description
The difference between day and night expression of SIRT in serum will be compared between the two arms.
Time Frame
48 hours after study enrollment.
Title
Changes in circadian rhythm assessed using cortisol.
Description
The difference between day and night concentrations of serum free cortisol will be compared between the two arms.
Time Frame
At least 48 hours after study enrollment.
Title
Changes in circadian rhythm assessed using insulin.
Description
The difference between day and night concentrations of serum insulin will be compared between the two arms.
Time Frame
At least 48 hours after study enrollment.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Admitted to the ICU Mechanically ventilated Receiving enteric feedings for at least 48 hours Exclusion Criteria: Pregnancy Previously diagnosed neurocognitive disorders, Alcohol withdrawal and history of alcohol dependence
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jag Sunderram, MD
Phone
732-235-7038
Email
sunderja@rwjms.rutgers.edu
Facility Information:
Facility Name
Robert Wood Johnson Medical School
City
New Brunswick
State/Province
New Jersey
ZIP/Postal Code
08901
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jag Sunderram, MD
Phone
732-235-7038

12. IPD Sharing Statement

Plan to Share IPD
No

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Effects of Feeding Schedule on the Development of ICU Delirium

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