Short-term And Longer-term Cognitive Impact Of Hourly Neurochecks In Acute Brain Injury

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The proposed research plan seeks to understand the impact of sleep disruption in the Neurological Intensive Care Unit (ICU) on older patients with acute brain injury (ABI). In current practice, the neurocritical care community performs frequent serial neurological examinations (neurochecks) in an effort to monitor patients for neurological deterioration following brain injury. Many neurocritical patients are older and/or cognitively fragile, and delirium is common. Although ICU delirium is multifaceted, frequent neurochecks may represent a modifiable risk factor if the investigators can better understand the risks and benefits of various neurocheck frequencies. This project will randomize patients with acute spontaneous intracerebral hemorrhage (ICH) to either hourly (Q1) or every-other-hour (Q2) neurochecks and evaluate the impact of neurocheck frequency on delirium. Second, longer-term cognitive outcomes will be investigated in patients with ICH randomized to Q1 versus Q2 neurochecks with the goal of identifying whether hourly neurochecks increase the risk for dementia.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 100
Healthy Volunteers: f
View:

• Adult patients (age \>18 years) with spontaneous acute \<45cc in volume with radiographic and clinical stability for ≥6 hours following admission to the ICU. These criteria are based on the literature and experience of the investigative team.

• Additional intraventricular hemorrhage (with or without external ventricular drain) is allowable.

• Only first admission to the NeuroICU during the hospitalization will be eligible.

⁃ a. any patient included in part 1 alive at 6 months post-discharge

Locations
United States
California
UC San Diego Health
RECRUITING
San Diego
Contact Information
Primary
Jamie N LaBuzetta
jlabuzetta@ucsd.edu
18582491331
Time Frame
Start Date: 2024-07-08
Estimated Completion Date: 2029-10-31
Participants
Target number of participants: 120
Treatments
Active_comparator: Hourly Neurochecks
Patients will be awakened hourly for their examinations
Experimental: Every-Other-Hour Neurochecks
Patients will be awakened every other hour for their examinations
Related Therapeutic Areas
Sponsors
Leads: University of California, San Diego

This content was sourced from clinicaltrials.gov