Collaborative Assessment of ICU Recovery Needs

NCT ID: NCT03513289

Last Updated: 2020-02-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

66 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-04-03

Study Completion Date

2019-03-15

Brief Summary

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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

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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).

Conditions

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Post-Intensive Care Syndrome

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Patient, Carer, and Clinician Interviews

This group/cohort consists of patients who experienced critical illness and were hospitalized in an ICU setting.

Patient, Carer, and Clinician Interviews

Intervention Type OTHER

Post-ICU follow-up interviews conducted over the phone, lasting between 30-60 minutes.

Interventions

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Patient, Carer, and Clinician Interviews

Post-ICU follow-up interviews conducted over the phone, lasting between 30-60 minutes.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. 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.
2. Patients who survived a critical illness, and their carers, who did not participate in a THRIVE program.
3. 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

* N/A
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Society of Critical Care Medicine

OTHER

Sponsor Role collaborator

Vanderbilt University Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Carla Sevin

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

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Carla M Sevin, M.D.

Role: PRINCIPAL_INVESTIGATOR

Vanderbilt University Medical Center

Locations

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Vanderbilt University Medical Center

Nashville, Tennessee, United States

Site Status

Australian and New Zealand Intensive Care Research Centre

Melbourne, Victoria, Australia

Site Status

Countries

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United States Australia

Other Identifiers

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172158

Identifier Type: -

Identifier Source: org_study_id

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