FrAILT: Functional Assessment in Liver Transplantation

Sponsor
Baylor Research Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT03870568
Collaborator
(none)
300
1
97.8
3.1

Study Details

Study Description

Brief Summary

In order to ensure the equity of the liver allocation process, it is important to create objective, scientifically validated markers of frailty in patients with end-stage liver disease that accurately predict patient outcomes. Many measures have been developed to assess this clinical state in elderly patients, but none have been applied to patients with cirrhosis, a population at increased risk for accelerated functional decline. This protocol is designed to learn more about the effects of functional status (also known as "frailty") in liver transplant patients and patient outcomes both before and after liver transplant.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Subjects in this study will be asked questions regarding functional status and ability to do activities at home. Subjects will also be asked to complete several physical tests to assess functional status. For example, subjects will be asked to stand up from a chair several times, balance with their feet together, and walk down a hall as quickly as possible. Subjects will also be asked to perform a hand grip strength test.

    Subjects will be assessed at baseline and at every clinic visit in the pre-transplant setting. Subjects will again be assessed at 3, 6, and 12 months post-transplant.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    300 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Functional Assessment in Liver Transplantation
    Actual Study Start Date :
    Oct 6, 2015
    Anticipated Primary Completion Date :
    Dec 1, 2023
    Anticipated Study Completion Date :
    Dec 1, 2023

    Outcome Measures

    Primary Outcome Measures

    1. Fried Frailty Index measurements in 300 patients with end-stage liver disease awaiting liver transplantation [5 years]

      Fried Frailty is calculated by combining into one score measurements of: Exhaustion: number of days patient felt exhaustion in the past 7 days Physical activity: has the subject performed any weight bearing activity in the past month? (Possible answers: yes or no). Grip strength test using dynamometer: Three measurements reported in kg. Walking speed in a 13-foot (4 meters) walk: Three measurements reported in seconds Unintentional Weight Loss: report if patient has lost 10 lbs or more in the last year. Minnesota Leisure Time Physical Activity Questionnaire (MNLTPA) calculated as a value of 1 for males with MNLTPA score less than 383 kcal/week and for females with a score less than 270 kcal/week. Range of score is 0 to 5 with 0 being not frail and 5 being most frail

    2. Liver Frailty Index measurements in 300 patients with end-stage liver disease awaiting liver transplantation [5 years]

      The following measurements are used individually to assess liver frailty index: Chair stands: The patient stands up from a sitting position without using his/her arms. The time (in seconds) the patient requires to complete the task is reported. Balance testing: patients must stand up in side by side, semi tandem and tandem positions for 10 seconds each. If the subject can't hold position for 10 seconds, the number of seconds that the subject kept in position is reported. Scoring range is 1.0 to 7.0 with 1.0 to 3.0 being "robust" and 4.5 to 7.0 being "frail"

    3. Numbers Connection test measurements in 300 patients with end-stage liver disease [5 years]

      Patient connects numbers that are scattered at random on a piece of paper. Reported as time (in seconds) taken to connect the numbers.

    4. Work status [5 years]

      Possible answers: working, retired, on disability, other.

    5. Hospitalizations [5 years]

      Possible answers: yes or no. If yes, report #of nights and reason.

    6. Activities of daily living (ADLs) [At 1 year post transplantation]

      Six questions about daily activities Scoring: A response of yes to any of the questions receives a value of 1. the ADL score is measured as the sum of the values of the 6 questions. A score of 0 correlates with "most dependent" and a score of 6 is "most independent."

    7. Instrumental Activities of Daily Living (IADLs) [At 1 year post transplantation]

      Eight questions about daily activities: Scoring: each question can be answered with a score of 0 or 1. The final iADL score is the sum of all values. The range of the score is 0 to 8 with 0 being most dependent and 8 being "most independent.'

    8. 36 Item Short Form Survey Instrument (SF-36) [At 1 year post transplantation]

      Patient will complete a 36 question questionnaire about quality of life at 1 year post transplantation.

    Secondary Outcome Measures

    1. Correlation between frailty and outcomes both before and after liver transplantation. [5 years]

      The association between the subject's frailty score and their pre and post transplant outcomes will be assessed.

    Other Outcome Measures

    1. Change in measurements of fried frailty before and after liver transplantation. [5 years]

      The changes in frailty score pre and post transplant will be evaluated.

    2. Change in measurements of liver frailty before and after liver transplantation. [5 years]

      The changes in frailty score pre and post transplant will be evaluated.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Adults (≥18 years old)

    • Listed for liver transplantation, or are "listable" - i.e, have undergone formal evaluation and been approved for listing if/when patients achieve high enough priority

    • Are seen in the outpatient clinic setting

    Exclusion Criteria:
    • Have severe hepatic encephalopathy at enrollment (defined by the time to complete the Numbers Connection Test (NCT) > 120 seconds, which is the first test that the participants complete upon enrollment).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Baylor University Medical Center Dallas Texas United States 75246

    Sponsors and Collaborators

    • Baylor Research Institute

    Investigators

    • Principal Investigator: James Trotter, MD, Baylor Health Care System

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Baylor Research Institute
    ClinicalTrials.gov Identifier:
    NCT03870568
    Other Study ID Numbers:
    • 015-243
    First Posted:
    Mar 12, 2019
    Last Update Posted:
    Jul 20, 2022
    Last Verified:
    Jul 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Baylor Research Institute
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 20, 2022