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Behavioral Intervention
Telemedicine ICU Recovery Clinic for Post Intensive Care Syndrome (TelePORT Trial)
N/A
Recruiting
Led By Leanne M Boehm, PhD
Research Sponsored by Vanderbilt University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
TelePORT Trial Summary
This trial focuses on studying the long-term cognitive impairment in patients after they have been in intensive care. The study aims to understand how this impairment affects patients' ability to live independently, work, and manage
Who is the study for?
This trial is for adults over 45 who were in a medical or surgical ICU, treated for acute respiratory failure with mechanical ventilation and/or septic shock with vasopressors. It's not suitable for those who don't meet these specific conditions.Check my eligibility
What is being tested?
The TelePORT Study is testing the use of telemedicine visits to help patients recover cognitive skills after intensive care. It aims to see if this can improve their ability to live independently and manage daily tasks.See study design
What are the potential side effects?
Since the intervention involves telehealth visits rather than medication, there are no direct physical side effects expected from participating in this study.
TelePORT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Cognitive function - MoCA
Cognitive function - PROMIS
Secondary outcome measures
Mental health - PTSD
Mental health - anxiety/depression
Physical function - ADL
+4 moreOther outcome measures
Post-Traumatic Growth
TelePORT Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Telemedicine ICU Recovery ClinicExperimental Treatment1 Intervention
scheduled telemedicine study visits 3 weeks and 3 months after hospital discharge or return-to-home if discharged to another facility
Group II: Standard Recovery Conditions (i.e., Control)Active Control1 Intervention
Control group participants will proceed with follow-up as determined by the discharging hospital team and directed to use the provided PICS guide to connect with commonly used resources.
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Who is running the clinical trial?
National Institute on Aging (NIA)NIH
1,699 Previous Clinical Trials
28,032,647 Total Patients Enrolled
Vanderbilt UniversityLead Sponsor
705 Previous Clinical Trials
6,143,221 Total Patients Enrolled
Ohio State UniversityOTHER
840 Previous Clinical Trials
509,489 Total Patients Enrolled
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