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Uncertainty Management Intervention

Primary Purpose

Liver Diseases

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Uncertainty Management Intervention
Comparison Conditions for Liver Transplant
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Liver Diseases focused on measuring liver disease, uncertainty, self management

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria (patient):

  • Diagnosis of ESLD and on the liver transplant waiting list
  • Receiving care at a Liver Clinic in the United States
  • 18 years of age or older
  • MELD greater than or equal to 11
  • Able to read and speak English
  • No major cognitive impairment
  • Not a recipient of a prior transplant (any organ)
  • Has a caregiver willing to participate

Inclusion Criteria (caregiver):

  • 18 years of age or older
  • Able to read and speak English
  • Provides care to a patient meeting the above criteria

Sites / Locations

  • The University of Nebraska Medical Center
  • University of North Carolina-Chapel Hill
  • Duke University
  • The University of Pittsburgh

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Uncertainty Management Intervention

Comparison Conditions for Liver Disease

Arm Description

The Uncertainty Management Intervention will consist of six 30-minute phone calls with a study educator to discuss issues of psychological distress, uncertainty management, symptom control, self efficacy for symptom management, and quality of life.

Six 30-minute telephone calls that provide structured education about liver disease.

Outcomes

Primary Outcome Measures

Uncertainty Management

Secondary Outcome Measures

Symptom control
Quality of life
Psychological distress

Full Information

First Posted
July 10, 2009
Last Updated
February 6, 2014
Sponsor
Duke University
Collaborators
National Institute of Nursing Research (NINR)
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1. Study Identification

Unique Protocol Identification Number
NCT00938795
Brief Title
Uncertainty Management Intervention
Official Title
Uncertainty Management Intervention for Patients Awaiting Liver Transplant
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
National Institute of Nursing Research (NINR)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this study is to improve symptoms and quality of life for end-stage liver disease patients awaiting a liver transplant and their caregivers by providing them with the resources and tools to self-manage their complex concerns.
Detailed Description
Hepatitis C Virus is the most common blood-borne infection in the U.S., affecting at least 4 million individuals, with more than 19,000 new cases occurring each year. Further, the CDC has projected a fourfold increase in the number of chronic hepatitis C patients between 1990 and 2015, and these patients are at risk for developing end stage liver disease (ESLD). By 2015 an estimated 375,000 chronic hepatitis C patients will develop cirrhosis and progress to ESLD, representing the majority of individuals who need liver transplants. ESLD is a life-limiting illness, and patients are told that, without a liver transplant, they may die. This 5 year randomized controlled trial will test the efficacy of an Uncertainty Management Intervention delivered via telephone by a nurse to the patient and caregiver. An attention control group of patients and caregivers will receive phone calls to discuss their experience of awaiting a liver transplant. Based on the problems and concerns of patients waiting for a liver transplant and the prior success of the Intervention for patients dealing with serious chronic illness, we believe the Uncertainty Management Intervention adapted specifically for ESLD patients will lead to significant improvements in patients' and caregivers' abilities to manage the symptoms and distress associated with ESLD and the process of awaiting liver transplant. The specific aims are to: 1) examine the effects of the Uncertainty Management Intervention on patient outcomes of psychological distress, uncertainty management, symptom control, self efficacy for symptom management, and QOL compared to an attention control group receiving calls to discuss their disease experience; 2) explore the effects of the Intervention on caregiver outcomes of uncertainty management, self-efficacy for helping the patient manage symptoms, and better QOL compared to an attention control group; 3) identify characteristics of individuals for whom the intervention is particularly effective. Waiting for a liver transplant under conditions of uncertainty is a harrowing experience for patients and caregivers, yet there have been few attempts to test nursing interventions for ESLD patients. The overall goal of this project is to provide these patients and their caregivers the tools to self-manage their complex concerns. The anticipated outcome is ESLD patients awaiting liver transplant benefit from the Uncertainty Management Intervention, thus providing new knowledge for practitioners and policy makers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Liver Diseases
Keywords
liver disease, uncertainty, self management

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
288 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Uncertainty Management Intervention
Arm Type
Other
Arm Description
The Uncertainty Management Intervention will consist of six 30-minute phone calls with a study educator to discuss issues of psychological distress, uncertainty management, symptom control, self efficacy for symptom management, and quality of life.
Arm Title
Comparison Conditions for Liver Disease
Arm Type
Other
Arm Description
Six 30-minute telephone calls that provide structured education about liver disease.
Intervention Type
Other
Intervention Name(s)
Uncertainty Management Intervention
Intervention Description
Six 30-minute telephone calls with a nurse to discuss emotional and physical aspects of liver disease and awaiting liver transplant
Intervention Type
Other
Intervention Name(s)
Comparison Conditions for Liver Transplant
Intervention Description
Six 30-minute telephone calls that provide structured education about liver disease.
Primary Outcome Measure Information:
Title
Uncertainty Management
Time Frame
Five months
Secondary Outcome Measure Information:
Title
Symptom control
Time Frame
Five months
Title
Quality of life
Time Frame
Five months
Title
Psychological distress
Time Frame
Five months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria (patient): Diagnosis of ESLD and on the liver transplant waiting list Receiving care at a Liver Clinic in the United States 18 years of age or older MELD greater than or equal to 11 Able to read and speak English No major cognitive impairment Not a recipient of a prior transplant (any organ) Has a caregiver willing to participate Inclusion Criteria (caregiver): 18 years of age or older Able to read and speak English Provides care to a patient meeting the above criteria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James Tulsky, MD
Organizational Affiliation
Duke University School of Nursing
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Donald Bailey, PhD
Organizational Affiliation
Duke University School of Nursing
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Annette Devito Dabbs, PhD, RN
Organizational Affiliation
The University of Pittsburgh
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Paul H. Hayashi, MD, MPH
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Laurel Williams-Salonen, RN,MSN,CCTC
Organizational Affiliation
The University of Nebraska Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Nebraska Medical Center
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
68198
Country
United States
Facility Name
University of North Carolina-Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States
Facility Name
Duke University
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705
Country
United States
Facility Name
The University of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15261
Country
United States

12. IPD Sharing Statement

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Uncertainty Management Intervention

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