- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01573325
HRQoL in the Low MELD Pre-tx Population (LowMELD)
February 27, 2014 updated by: Rebecca Duke, Northwestern University
Health-Related Quality of Life in the Low Model for End-Stage Liver Disease (MELD) Pre Transplant Patient Candidate: A Pilot Study
The purpose of this study is to describe the HRQoL in those with MELD scores </= 15 in a single center for those who are pre-liver transplant candidates
Study Overview
Status
Completed
Conditions
Detailed Description
The liver organ allocation system was significantly revised in 2002, allowing a more objective prioritization of liver transplant candidates.
The revised Model for End Stage Liver Disease (MELD) system is based primarily on laboratory test results.
Candidates with MELD scores of less than 15 are considered to be low priority for cadaveric liver transplant and have limited treatment options.
Yet patients with low MELD scores may suffer from an array of symptoms associated with liver disease such as fatigue, sleep disturbances, and depression - all of which erode health-related quality of life (HRQoL).
No previous studies were found that examined HRQoL in low MELD transplant patients.
A better understanding of the HRQoL of these patients will allow clinicians to better meet their needs.
Therefore, the aims of the proposed pilot capstone project are to examine HRQoL and to identify demographic and clinical characteristics including liver-disease related symptoms, functional status, perceived social support, biological functioning and mental health associated with HRQoL in pre-liver transplant candidates with low MELD scores.
The revised Wilson and Cleary Quality of Life Model will be used to guide the project.
Fifty pre-transplant liver candidates with MELD scores < 15 will be enrolled in the descriptive, cross-sectional pilot study.
Participants will complete a written questionnaire measuring perceived HRQoL and clinical characteristics.
Descriptive and correlational statistics will be used to analyze the data.
Findings from this project will identify trends in factors that contribute to a HRQoL of this population and provide the foundation for a larger future project.
Study Type
Observational
Enrollment (Actual)
50
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 75 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adults who are a candidate for a liver transplant at Northwester Memorial Hospital with MELD score </=15
Description
Inclusion Criteria:
- Must be a patient in the liver transplant clinic at Northwestern Memorial Hospital or one of its satellite clinics (including Washington, Illinois; Portage, Indiana; Glenview, Illinois, Oakbrook, Illinois; Joliet, Illinois)
- Adult patient between the ages of 18-75
- Ability to read and speak English
- Must be a candidate for liver transplant per Northwestern Memorial Hospital liver transplant multidisciplinary committee
- Model for End Stage Liver Disease (MELD) score ≤15
- Cognitive ability to complete measures
Exclusion Criteria:
- Non-English speaking
- Those who have already received a liver transplant
Hepatic encephalopathy as evidenced by:
- Grade II or more West Haven Criteria or Adapted West Haven Criteria
- Evidence of Asterixis upon exam at time of consent (if consented in person)
- Acute liver failure as etiology for liver disease.
- MELD score > 15
- Mental retardation or cognitive disabilities preventing completion of the written questionnaire
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived HRQoL Score. Overall Qualty of Life Index Tool Was Utilized.
Time Frame: 2-3 months
|
Describe perceived HRQoL in patients with low MELD scores (≤15) pre-liver transplant patient population.
Overall Qualty of Life Index tool was utilized.
The subscales were not utilized.
The unit of measurement was scores on a scale.
QLI tool has a range of 0-30 for total possible score.
With the higher the score the higher the HRQoL.
|
2-3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of Subjects With Depressive Scores Who Had a Poor HRQoL
Time Frame: 2-3 months
|
Identify clinical characteristics such as environmental factors, patient biology, liver-disease related symptoms, functional status, general health perception, characteristics of the individual associated with perceived HRQoL in patients with low MELD scores (≤15) pre-transplant.
What characteristics were found to be predictive of poor HRQoL.
Tools utilized each assessed the specific variables including patient biology, liver disease symptoms, functional status, general health perception, and characteristics of the individual.
|
2-3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Rebecca Duke, MSN, Northwestern University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
March 1, 2012
Primary Completion (ACTUAL)
July 1, 2012
Study Completion (ACTUAL)
July 1, 2012
Study Registration Dates
First Submitted
April 5, 2012
First Submitted That Met QC Criteria
April 5, 2012
First Posted (ESTIMATE)
April 9, 2012
Study Record Updates
Last Update Posted (ESTIMATE)
February 28, 2014
Last Update Submitted That Met QC Criteria
February 27, 2014
Last Verified
February 1, 2014
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- STU00060397
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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