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Clinical Trials/NCT03513289
NCT03513289
Completed
N/A

Collaborative Assessment of ICU Recovery Needs

Vanderbilt University Medical Center2 sites in 2 countries66 target enrollmentApril 3, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Post-Intensive Care Syndrome
Sponsor
Vanderbilt University Medical Center
Enrollment
66
Locations
2
Primary Endpoint
Survivorship Experiences from Patients
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The primary purpose of this study is to better understand the impact of the Society of Critical Care Medicine (SCCM) THRIVE Collaboratives on patients, their families and clinicians.

The investigators have formed an international and interprofessional evaluative team with experts in the field in an effort to explore interactions between survivors and THRIVE. This approach is reflective of the international ethos of SCCM and its collaboratives, with the potential to improve the generalizability of this survivorship research to different health systems.

Detailed Description

The aims of this qualitative study are: 1. To identify elements that helped survivors in their recovery, as well as potential obstacles 2. To capture elements of survivorshop that are generalizable, regardless of participation in the THRIVE collaboratives 3. To gain knowledge to be incorporated back into the collaboratives Patients, family members, and clinicians will be interviewed and their responses analyzed for themes of ICU recovery including elements that patients and families find helpful to recovery, barriers and facilitators to different models of post-ICU support, including peer support and post-ICU clinics, and drivers of improvement in post-ICU care. Patients, carers, and clinicians with a wide variety of survivorship experiences are encouraged to participate, including those who have participated in a THRIVE collaborative support site (peer support or clinic).

Registry
clinicaltrials.gov
Start Date
April 3, 2018
End Date
March 15, 2019
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Carla Sevin

Assistant Professor of Medicine, Director of the ICU Recovery Center at Vanderbilt

Vanderbilt University Medical Center

Eligibility Criteria

Inclusion Criteria

  • Patients who survived a critical illness, and their carers, who were identified by collaborative members or self-identify as having been through a THRIVE Program.
  • Patients who survived a critical illness, and their carers, who did not participate in a THRIVE program.
  • Clinicians directly involved in the care of ICU survivors in the outpatient setting, who have participated in a THRIVE initiative through the Society of Critical Care Medicine.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Survivorship Experiences from Patients

Time Frame: 18 months

30-minute audio-taped, semi-structured interviews with patients informing on post-ICU care coordination

Secondary Outcomes

  • Survivorship Experiences from Clinicians(18 months)
  • Survivorship Experiences from Caregivers(18 months)

Study Sites (2)

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