Actively Recruiting
Telehealth-enhanced Patient-oriented Recovery Trajectory After Intensive Care
Led by Vanderbilt University · Updated on 2025-06-12
202
Participants Needed
2
Research Sites
220 weeks
Total Duration
On this page
Sponsors
V
Vanderbilt University
Lead Sponsor
N
National Institute on Aging (NIA)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Intact cognitive skills are necessary for independent living, going to work, and managing finances, and any loss of cognitive skills places a burden on society akin to what is seen with Alzheimer's Disease and Related Dementias. The TelePORT Study (Telehealth-Enhanced Patient-Oriented Recovery Trajectories after Intensive Care) is the first post-intensive care syndrome longitudinal long-term cognitive impairment intervention study. The societal effect from long-term cognitive impairment after critical illness is great as many of these patients are employable adults or functional retirees.
CONDITIONS
Official Title
Telehealth-enhanced Patient-oriented Recovery Trajectory After Intensive Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 45 years or older
- Admitted to a medical or surgical intensive care unit (ICU)
- Treated for acute respiratory failure with mechanical ventilation and/or septic shock with vasopressors
You will not qualify if you...
- Receiving hospice care at discharge or not expected to survive 6 months
- No access to a computer or electronic device (tablet, smartphone) with cellular or WiFi for telemedicine visits
- Substance abuse or psychiatric disorder preventing independent living
- Unable to speak English
- Severe dementia preventing independent living before hospitalization
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
Ohio State University Wexner Medical Center
Columbus, Ohio, United States, 43210
Not Yet Recruiting
2
Vanderbilt University Medical Center
Nashville, Tennessee, United States, 37232
Actively Recruiting
Research Team
L
Leanne M Boehm, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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