Skip to main content
Clinical Trials/NCT02560129
NCT02560129CompletedNot Applicable

Evaluation of Outcomes Following Critical Illness Through a MICU Recovery Clinic

Wake Forest University Health Sciences1 site in 1 country14 target enrollmentStarted: July 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
14
Locations
1
Primary Endpoint
Physical Function

Study Overview

Brief Summary

Summary: Emerging data demonstrate long-term morbidity and mortality in those who survive critical illness. However, there is no data regarding long-term follow-up for ICU survivors. The investigators have begun the implementation of an ICU recovery clinic.

Rationale:

ICU survivors are at high risk for functional, cognitive and psychiatric impairments. However, methods to mitigate these impairments and improve recovery are lacking. Special follow-up clinics for survivors of critical illness have been proposed and implemented to some degree, but are uncommon.

Detailed Description

Objectives:

  1. To evaluate physical function, cognitive function, and overall functional status during recovery from critical illness.
  2. To evaluate anxiety, depression, and PTSD during recovery from critical illness.
  3. To evaluate resilience during recovery from critical illness.
  4. To evaluate healthcare utilization rates, morbidity, and mortality following critical illness.
  5. Added April 2016: To study the voice and swallowing function of patients following recovery from critical illness.
  6. Added April 2016: To study the pain of patients following recovery from critical illness.

Intervention:

A prospective observational study of all patients who attend our ICU recovery clinic.

Methods:

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Wake Forest MICU Admission
  • sepsis OR
  • respiratory failure requiring >24 hrs of invasive mechanical ventilation
  • previously functional

Exclusion Criteria

  • Active Malignancy

Outcomes

Primary Outcomes

Physical Function

Time Frame: 6 months

as measured by the Short Performance Physical Battery

Secondary Outcomes

  • Cognitive Function(6 months)
  • Resilience(6 months)
  • Hospital Readmissions(6 months)
  • Anxiety/ Depression Screening(6 months)
  • Quality of Life(6 months)
  • Physical Function(6 months)
  • Post Traumatic Stress Disorder Screening(6 months)
  • Functional Status(6 months)
  • Mortality(6 months)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials