RECRUITING

Telehealth-enhanced Patient-oriented Recovery Trajectory After Intensive Care

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Telehealth-enhanced Patient-oriented Recovery Trajectory After Intensive Care

Quick Facts

Study Start:2024-03-13
Study Completion:2028-05-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06014931

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:45 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults (age ≥45)
  2. * Admitted to a medical or surgical ICU
  3. * Treated for ARF (with mechanical ventilation) and/or septic shock (with vasopressors)
  1. * hospice care at discharge or not expected to survive 6 months
  2. * no access to a computer or electronic device (e.g., tablet, smart phone) with cellular or WiFi connection for a telemedicine clinic visit
  3. * substance abuse or psych disorder that prevents independent living
  4. * inability to speak English
  5. * severe dementia preventing independent living prior to index hospitalization

Contacts and Locations

Study Contact

Leanne M Boehm, PhD
CONTACT
615-343-1051
leanne.boehm@vanderbilt.edu

Principal Investigator

Leanne M Boehm, PhD
PRINCIPAL_INVESTIGATOR
Vanderbilt University

Study Locations (Sites)

Ohio State University Wexner Medical Center
Columbus, Ohio, 43210
United States
Vanderbilt University Medical Center
Nashville, Tennessee, 37232
United States

Collaborators and Investigators

Sponsor: Vanderbilt University

  • Leanne M Boehm, PhD, PRINCIPAL_INVESTIGATOR, Vanderbilt University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-03-13
Study Completion Date2028-05-31

Study Record Updates

Study Start Date2024-03-13
Study Completion Date2028-05-31

Terms related to this study

Additional Relevant MeSH Terms

  • Post-intensive Care Syndrome