Self-Management Behaviors of Caregivers of the Chronically Critically Ill (ASSIST)
Critical Illness
About this trial
This is an interventional supportive care trial for Critical Illness focused on measuring caregiver, chronically critically ill
Eligibility Criteria
Inclusion Criteria:
- aged 18 years or older
- recognized as the family member who will assume the caregiver role for a critically ill adult requiring at least 72 hours of mechanical ventilation and scheduled for a discharge to an extended care facility
- speak and comprehend English
Exclusion Criteria:
- currently practicing mindfulness-based interventions
- require psychotherapy or required psychotherapy within the last three months
- have a history of dementia or major neurological illness
- pregnant
- history of medical conditions or procedures that is contraindicated for fMRI scanning
- claustrophobia requiring anxiolytics or sedation
- expected to relocate from Northeast Ohio within two months
Sites / Locations
- University Hospitals Case Medical Center
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
ASSIST
Attention-Control
The ASSIST intervention will deliver daily doses of MMT and vary dose intensity of all components each day based on the subject's biophysical data. Across a 30-day period, the ASSIST intervention will capture and analyze data to deliver on-demand MMT, guided practices to promote sleep hygiene and physical activity. Each day, subjects will receive at least one prompt to practice MMT (about 5 minutes at a time). However, based on the subject's biophysical sensor data, subjects could receive a maximum of 5 alerts or prompts per day from the device to enhance stress reduction, sleep hygiene, or physical activity.
This intervention exposes subjects to the wearable technology without the self-management components to minimize novelty effects. Subjects assigned to this condition will wear the device for 30 days, which offers them an opportunity to experientially learn to self-monitor and employ self-regulatory skills by viewing the display biophysical data. Subjects in this condition will not receive any prompts from the device.