Improving sleep in acute respiratory failure survivors
B
Babar Khan, MD
Primary Investigator
Enrolling By Invitation
18-100 years
All
Phase
N/A
20 participants needed
3 Locations
Brief description of study
The purpose of this study is to evaluate the impact of a sleep deprivation and disruption on quality of life of acute respiratory failure ICU survivors using sleep actigraphy. Sleep actigraphy is a method of measuring sleep parameters and average motor activity over a period of days to weeks using a device worn on the wrist. The information provided can help characterize sleep patterns in this population, and guide future studies on treatment of sleep disorders after being discharged from intensive care.
Detailed description of study
Participants will be asked to complete questionnaires about their sleep and have an actigraph placed on their wrist. Participants will be asked to return the actigraph after two weeks. Some participants will be asked to complete a sleep study in addition to wearing the actigraph.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: acute respiratory failure
-
Age: Between 18 Years - 100 Years
-
Gender: All
Inclusion Criteria:
- Hospitalized in the ICU
- Diagnosed with Acute Respiratory Failure (ARF) requiring greater than or equal to 24 hours of mechanical ventilation
- Discharged to home, skilled nursing facility, sub-acute rehabilitation care, or long-term acute care
- English speaking
- Able to consent either in-person or through legally authorized representative
- Have access to a telephone
Exclusion Criteria:
- Hospitalized to a regular non-ICU ward
- Diagnosis of cancer with life expectancy less than 1 year
- Admitted with ischemic or hemorrhagic cerebrovascular accident, traumatic brain injury, or undergoing neurosurgery
- History of dementing illnesses and other neurodegenerative disease such as Alzheimer’s disease, Parkinson’s disease, or vascular dementia
- Unable to complete study questionnaire due to severe hearing loss
- Legally blind
- Pregnant (assessed by urine pregnancy test) or nursing
- Living outside the greater Indianapolis area
- Recent history of alcohol or substance abuse
- Status post tracheostomy and not eligible for a speaking valve
- Incarcerated at the time of study enrollment
Updated on
01 Aug 2024.
Study ID: 12582, PULM-IIR-SLEEP-POST-ICU
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