Study Results
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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COMPLETED
14 participants
OBSERVATIONAL
2015-07-31
2023-11-30
Brief Summary
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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.
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Detailed Description
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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:
Patients will be identified for participation in our ICU Recovery Clinic during their admission to the Wake Forest Baptist Medical Center Medical Intensive Care Unit (MICU). They will be asked to return to the ICU recovery clinic within 1 month of hospital discharge. Structured clinic visits as standard of care will include medication reconciliation and evaluation by a pharmacist, along with an evaluation by a clinic physician to address acute medical issues and provide counselling. They will also undergo standardized testing to evaluate physical function, cognitive function, and psychiatric function. Added April 2016: They will also undergo a standardized evaluation of speech, swallow, and pain.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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ICU Survivors
ICU survivors will be seen in a MICU Recovery Clinic where Questionnaires, Physical and Cognitive Function assessments will be measured
Questionnaires, Physical and Cognitive Function
ICU survivors will be administered a battery of questionnaires. Measurements of physical and cognitive function will also be performed.
Interventions
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Questionnaires, Physical and Cognitive Function
ICU survivors will be administered a battery of questionnaires. Measurements of physical and cognitive function will also be performed.
Eligibility Criteria
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Inclusion Criteria
* respiratory failure requiring \>24 hrs of invasive mechanical ventilation
* previously functional
Exclusion Criteria
ALL
No
Sponsors
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Wake Forest University Health Sciences
OTHER
Responsible Party
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Principal Investigators
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D. Clark Files, MD
Role: PRINCIPAL_INVESTIGATOR
Wake Forest University Health Sciences
Locations
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Wake Forest Baptist Medical Center
Winston-Salem, North Carolina, United States
Countries
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Other Identifiers
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IRB00031295
Identifier Type: -
Identifier Source: org_study_id
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