RECRUITING

Pharmacist-Intensivist Collaborative Telehealth for Post-Intensive Care Syndrome

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

The goal of this pilot randomized controlled trial is to determine if a randomized controlled trial of a collaborative pharmacist-intensivist telehealth follow-up after intensive care unit discharge can feasibly be performed in patients who have survived a critical illness. The study intervention will be telehealth follow-up appointments provided by clinical pharmacists at approximately one and three months post-hospital discharge. The purpose of the follow-up appointments will be to assess for post-intensive care syndrome and provide recommend interventions aimed at improving recovery Participants will randomized to receive the study intervention or standard of care.

Official Title

Pharmacist-Intensivist Collaborative Telehealth for Post-Intensive Care Syndrome in Survivors of Critical Illness: a Pilot Randomized Controlled Trial

Quick Facts

Study Start:2025-06-01
Study Completion:2026-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06983496

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:18 Years to 89 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adults 18-89 years of age
  2. * Required admission to either medical or surgical ICU
  3. * Respiratory failure requiring invasive mechanical ventilation of at least 24 hours during ICU stay; or ICU stay of at least 7 days
  4. * Anticipated discharge to home after hospitalization
  5. * Consent from patients themselves or a legally authorized representative if necessary
  1. * Pregnancy
  2. * Incarceration/Imprisonment
  3. * Life expectancy less than 6 months or enrolled in hospice/palliative care
  4. * Anticipated discharge to skilled nursing facility, medical rehabilitation facility, or other long terms care facility
  5. * Unable to participate in telehealth

Contacts and Locations

Study Contact

Andrew J Franck, Pharm.D.
CONTACT
3523761611
Andrew.Franck@va.gov

Study Locations (Sites)

Malcom Randall Veterans Affairs Medical Center
Gainesville, Florida, 32608
United States

Collaborators and Investigators

Sponsor: Malcom Randall VA Medical Center

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 Date2025-06-01
Study Completion Date2026-12

Study Record Updates

Study Start Date2025-06-01
Study Completion Date2026-12

Terms related to this study

Additional Relevant MeSH Terms

  • Post Intensive Care Syndrome (PICS)