- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06729502
Pictorial Fit-Frail Scale in Adults Admitted to the ICU in a Tertiary Center- an Observational Prospective Study
Pictorial Fit-Frail Scale in Adults Admitted to the Intensive Care Unit in a Tertiary Center- an Observational Prospective Study
Understanding the frailty levels of critically ill patients using the PFFS at time of admission to ICU.
Exploring any associations between frailty, other prognostic factors, and patient outcomes.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Frailty is a state of high vulnerability for adverse health outcomes, including disability, dependency, falls, need for long-term care, and mortality. Several definitions exist, but all measure one's vulnerabilities, strengths, and indirectly assess the physiological reserve. Frailty is not necessarily age dependent, but some of its domain are affected by age. In recent years, frailty has increasingly been recognized as an important factor in the prognosis assessment of an older critically ill patient, in terms of mortality (both in-hospital and long term), hospital length of stay (LOS) and discharge disposition. A previous study performed in Rabin Medical Center ICU demonstrated a strong association between frailty in 90-d mortality of critically ill patients. Frailty is also associated with a higher risk of persistent clinical illness (critical care dependency for survival).
There are several methods for frailty assessment; the comprehensive geriatric assessment is considered the gold standard. However, this method takes time, and requires full patient cooperation, both are usually not possible at the time of critical illness. Several other valeted methods are commonly used, including the Clinical Frailty Scale (CFS), Frailty Index, Frailty phenotype, simple FRAIL questionnaire modified frailty index, and many more.These tools have been validated in different settings, and were found related to several outcomes. There are several differences between the different tools. Some require clinical assessment (with or without patients cooperation), while others require only a review of the healthcare record (EHR). Nevertheless, there are differences between these tools in sensitivity, and specificity in terms of screening and diagnosis of frailty and the contributing factors to the state of frailty.
In 2019 the pictorial fit-frail scale (PFFS) has been introduced as a quick and easy-to-use tool for frailty assessment. It takes few minutes to fill by the patient or caregiver, it's not based on language or health literacy, and requires no clinical examination by the medical staff. The PFFS was validated in several clinical settings, including thoracic surgery clinic, geriatric clinic, memory clinic, and primary care clinics.
PFFS has been assessed in the critical care setting in our unit and was found associated with longer term mortality. The PFFS questionnaire has become a standard of care upon admission to our ICU. This study aims to describe the PFFS scores patients over 60 years old, its correlation with other prognostic scores, and its association with patients' outcomes (ICU length of stay, length of ventilation, ICU mortality, 90days mortality).
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Liran Statlender, MD
- Phone Number: +97239376590
- Email: liranst1@clalit.org.il
Study Locations
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Petach Tikva, Israel
- Recruiting
- Rabin Medical Center
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Contact:
- Liran Statlender
- Phone Number: +97239376590
- Email: liranst1@clalit.org.il
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Older adults (age ≥ 60 years) who were admitted to the ICU for more than 24 hours at the participating centers
Exclusion Criteria:
- Prior recent admission to an ICU (within 30 days)
- Admissions for brain death evaluation.
- Planned admissions to the ICU (i.e for percutaneous tracheostomy, for specific treatment under sedation).
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
90-d mortality
Time Frame: up to 90 days from ICU admission
|
Mortality at 90 days from ICU admission
|
up to 90 days from ICU admission
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
ICU mortality
Time Frame: During index admission
|
Mortality during index admission at the ICU
|
During index admission
|
|
Hospital mortality
Time Frame: During index admission
|
Mortality during hospital admission
|
During index admission
|
|
ICU length of stay
Time Frame: up to 90 days from ICU admission
|
Duration of ICU admission
|
up to 90 days from ICU admission
|
|
Hospital length of stay
Time Frame: Up to 90 days from ICU admission
|
Duration of hospital admission
|
Up to 90 days from ICU admission
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 0377-24-RMC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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