Pharmacist-Intensivist Collaborative Telehealth for Post-Intensive Care Syndrome

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-89
SponsorMalcom Randall VA Medical Center

About this trial

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.

Eligibility criteria

Qualifiers

Adults 18-89 years of age

Required admission to either medical or surgical ICU

Respiratory failure requiring invasive mechanical ventilation of at least 24 hours during ICU stay; or ICU stay of at least 7 days

Anticipated discharge to home after hospitalization

Disqualifiers

Pregnancy

Incarceration/Imprisonment

Life expectancy less than 6 months or enrolled in hospice/palliative care

Anticipated discharge to skilled nursing facility, medical rehabilitation facility, or other long terms care facility

Trial design

Treatments tested in this trial

  • Post-ICU Telehealth Follow-up

Treatment groups

24 Participants
are divided into 2 treatment groups