Purpose

The investigators are performing this research study to understand the role of sleep disturbance on the incidence/severity of delirium after surgery. The investigators will study the brain using a polysomnography device (PSG), which records the brain's electrical activity during sleep.

Condition

Eligibility

Eligible Ages
Between 60 Years and 100 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Over 60 years of age - Inpatient and scheduled for surgical procedure at MGH

Exclusion Criteria

  • Blindness, deafness or the inability to speak English - Inability to provide informed consent Objective Drop Criteria - Post-operative intubation greater than 24 hours

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
MGH Surgery Patients PSG data will be collected, and delirium assessments conducted, on patients undergoing surgery at MGH.
  • Device: PSG
    PSG data to be collected on the night before surgery to establish level of preexisting sleep disturbance.

More Details

Status
Completed
Sponsor
Massachusetts General Hospital

Study Contact

Detailed Description

During this study, PSG recordings will be collected and a sleep questionnaire will be administered to participants on the night before surgery in order to establish level of preexisting sleep disturbance. Delirium assessments will be conducted during the postoperative period. On postoperative days 0 and 1, blood will be collected for analysis. Further cognitive, quality of life and pain questionnaires will be administered perioperatively.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.