Assessment of Verbal Comprehension and Cognitive Processes in Patients Admitted to the Palliative and Supportive Care Unit

Sponsor
M.D. Anderson Cancer Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT05091632
Collaborator
(none)
30
1
25.9
1.2

Study Details

Study Description

Brief Summary

This study investigates the use electroencephalography (EEG - a test that measures brain waves) to learn if patients who appear unresponsive (do not respond to noises, words, or touch) retain any consciousness. Families want to know if their loved ones who are unresponsive can still hear them or feel any discomfort. Information gained from this study may have important impact in how patients, caregivers, and doctors make decisions.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Electroencephalography
  • Other: Questionnaire Administration

Detailed Description

PRIMARY OBJECTIVES:
  1. To estimate the magnitude of electroencephalography (EEG) response to verbal stimuli among cancer patients in the last days in life admitted to a palliative and supportive care unit (PSCU).

  2. To examine the feasibility of conducting EEG in cancer patients in the last days of life.

SECONDARY OBJECTIVES:
  1. To compare the magnitude of EEG response between impending death cohort and control cohort.

  2. To determine the association between the magnitude of EEG response and clinical assessments (e.g. JFK Coma Recovery Scale-Revised [CRS-R], Glasgow Coma Scale [GCS], Richmond Agitation Sedation Scale [RASS], Memorial Delirium Assessment Scale [MDAS]) in impending death cohort and control cohort separately.

  3. To determine the magnitude of EEG response to pressure/noxious stimuli in impending death cohort and control cohort separately.

  4. To examine serial EEG changes in auditory cortex activation and cognitive processing in cancer patients over the last days of life.

OUTLINE:

Patients undergo EEG over 30 minutes daily until death or discharge and complete questionnaires over 30 minutes daily until death or discharge to check level of consciousness, thought, and ability to communicate.

Study Design

Study Type:
Observational
Anticipated Enrollment :
30 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Can You Hear Me? Assessment of Verbal Comprehension and Cognitive Processes in Patients in the Last Days of Life
Actual Study Start Date :
May 4, 2021
Anticipated Primary Completion Date :
Jun 30, 2023
Anticipated Study Completion Date :
Jun 30, 2023

Arms and Interventions

Arm Intervention/Treatment
Observational (EEG, questionnaires)

Patients undergo EEG over 30 minutes daily until death or discharge and complete questionnaires over 30 minutes daily until death or discharge to check level of consciousness, thought, and ability to communicate.

Procedure: Electroencephalography
Undergo EEG
Other Names:
  • EEG
  • electroencephalogram
  • Other: Questionnaire Administration
    Complete questionnaires

    Outcome Measures

    Primary Outcome Measures

    1. Magnitude of electroencephalography (EEG) response to verbal stimuli among impending death cancer patients [Day 1 in palliative and supportive care unit]

      The magnitudes of EEG responses in each task will be calculated as the difference between pre-stimulus and post-stimulus, separately. 95% confidence intervals will be estimated for each task.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • BOTH COHORTS: Diagnosis of advanced cancer (defined as locally advanced, metastatic, recurrent, or incurable disease)

    • BOTH COHORTS: Admitted to the PSCU at MD Anderson Cancer Center

    • IMPENDING DEATH COHORT: Clinician judgement of =< 3 days of survival or >= 1 late sign of impending death

    • Presence of late signs of impending death are based on reporting by bedside nurses, physicians, or research staff. Examples of these signs include inability to close eyelids; non-reactive pupils; drooping of nasolabial fold; hyperextension of neck; death rattle; grunting of vocal cords; decreased response to verbal/visual stimuli; respiration with mandibular movement; Cheyne Stokes breathing; pulselessness of radial artery; peripheral cyanosis; or decreased urine output

    • IMPENDING DEATH COHORT: Glasgow Coma Scale =< 8

    • IMPENDING DEATH COHORT: Not been able to communicate for past 24 hours (no verbal response) because of delirium, coma, or impending death based on the judgement of the palliative care unit physician.

    • IMPENDING DEATH COHORT: Palliative Performance Scale score of 10-20%

    • CONTROL COHORT: Able to communicate for the past 24 hours

    • CONTROL COHORT: Clinician judgement of >= 1 month of survival

    • BOTH COHORTS: English-speaking

    Exclusion Criteria:
    • BOTH COHORTS: Evidence of brain metastases, brain hemorrhage, or subdural hematomas on recent neuroimaging

    • BOTH COHORTS: Hearing impairment as documented by chart or requiring hearing aid

    • IMPENDING DEATH COHORT: Mental status changes predominantly related to medications as per clinician judgement

    • CONTROL COHORT: Diagnosis of delirium (i.e. Memorial Delirium Assessment Scale [MDAS]

    = 13)

    • BOTH COHORTS: Pregnant women

    • BOTH COHORTS: Age < 18 years old

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 M D Anderson Cancer Center Houston Texas United States 77030

    Sponsors and Collaborators

    • M.D. Anderson Cancer Center

    Investigators

    • Principal Investigator: David Hui, M.D. Anderson Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    M.D. Anderson Cancer Center
    ClinicalTrials.gov Identifier:
    NCT05091632
    Other Study ID Numbers:
    • 2019-1079
    • NCI-2021-08958
    • 2019-1079
    First Posted:
    Oct 25, 2021
    Last Update Posted:
    Jul 14, 2022
    Last Verified:
    Jul 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 14, 2022