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Improving Pain Management and Opioid Safety for Patients With Cirrhosis

Primary Purpose

Cirrhosis, Liver

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Liver Education About Pain (LEAP)
Usual Care
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Cirrhosis, Liver focused on measuring liver diseases, cirrhosis, liver, implementation science, strategies, evaluation, behavioral intervention

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All participants must be over 18 years of age and fluent in English
  • Must have a diagnosis of cirrhosis
  • Must be receiving care at UPMC hepatology clinics
  • Must have chronic pain lasting at least 3 months

Exclusion Criteria:

  • Participants will be excluded if they are younger than 18 years of age or are unable to provide informed consent for any reason
  • Participants will be excluded if they had a prior liver transplantation or have a limited life expectancy of less than 6 months

Sites / Locations

  • University of Pittsburgh Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

LEAP Intervention Arm

Usual Care

Arm Description

Half of the recruited patients (anticipate 20) will participate in 12 weekly sessions to teach self-pain management tools and skills. In addition to alternating weeks of group and individual sessions, participants will track their activities using the LEAP workbook provided during the first meeting, as tracking is a key component of most pain-self management interventions and is intended to address self-regulation. All patients can continue to use other pain management strategies ("usual care") in order to mimic real-life conditions.

Half of the recruited patients (anticipated 20) will receive usual care under the control arm of this study. These participants will not receive the intervention.

Outcomes

Primary Outcome Measures

Number of participants attending ≥80% of intervention sessions
Attendance will be studied by combining participant completion of follow-up measures and attending ≥80% of intervention sessions.
Overall Satisfaction
The primary acceptability outcome will be overall satisfaction with the intervention and will be operationalized using the Client Satisfaction Questionniare-8, an 8-item Likert-based general satisfaction measure that sums to a score of 8 to 32. A total score of ≥24, indicating an average score of "satisfied" across items, in at least 80% of participants will be operationalized as "acceptable."

Secondary Outcome Measures

Full Information

First Posted
October 18, 2021
Last Updated
March 16, 2023
Sponsor
University of Pittsburgh
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT05128578
Brief Title
Improving Pain Management and Opioid Safety for Patients With Cirrhosis
Official Title
Improving Pain Management and Opioid Safety for Patients With Cirrhosis: Pilot Program
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 14, 2022 (Actual)
Primary Completion Date
September 1, 2023 (Anticipated)
Study Completion Date
March 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This project aims to test a behavioral intervention in patients with liver cirrhosis and chronic pain and teach self pain-management skills.
Detailed Description
Prescription opioid medications are a leading cause of opioid-related death and are particularly risky in patients with cirrhosis of the liver, which affects 4 million people in the US. In this population, prescription opioids are associated with complications of liver disease, decreased access to life-saving transplantation, and increased hospitalization, post-transplant mortality, and all-cause mortality. Moreover, most patients with cirrhosis have underlying alcohol and/or substance use disorders (SUDs), which increase the risk of opioid-related complications and misuse. Despite these risks, our pilot work found that nearly half of all patients with cirrhosis are prescribed opioid medications each year and that these prescriptions are often inconsistent with opioid prescribing safety guidelines. One potential reason for this may be the lack of safe, evidence-based, alternative pain management strategies for this patient population. Indeed, existing opioid safety and pain management interventions designed for general populations do not address many of the specific issues facing patients with cirrhosis. The research team plans to recruit patients at UPMC for participation in the Liver Education About Pain (LEAP) intervention program. LEAP is a modular 12-week pain self-management intervention with alternating group and individual sessions. Group sessions allow participants to practice skills, set goals with the group, seek social support, and learn together. Individual sessions serve the purpose of individualizing the program to the needs of the patients. The purpose of the LEAP program is to make pain better, help patients reach their personal goals (things that may be hard to do because of pain), and add to the care patients' medical team is providing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cirrhosis, Liver
Keywords
liver diseases, cirrhosis, liver, implementation science, strategies, evaluation, behavioral intervention

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The Liver Education About Pain (LEAP) is a modular 12-week pain self-management intervention with alternating group and individual sessions. Group sessions allow participants to practice skills, set goals with the group, seek social support, and learn together. Individual sessions serve the purpose of individualizing the program to the needs of the patients. The purpose of the LEAP program is to make pain better, help patients reach their personal goals (things that may be hard to do because of pain), and add to the care patients' medical team is providing.
Masking
None (Open Label)
Masking Description
Enrolled participants will be randomized to one of two study arms (intervention or usual care) using permuted block randomization at the patient level, stratified by prescription opioid analgesia in the last year. The study statistician will develop the randomization schedule using standard randomization procedures, mimicking the anticipated randomization in the efficacy trial
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
LEAP Intervention Arm
Arm Type
Experimental
Arm Description
Half of the recruited patients (anticipate 20) will participate in 12 weekly sessions to teach self-pain management tools and skills. In addition to alternating weeks of group and individual sessions, participants will track their activities using the LEAP workbook provided during the first meeting, as tracking is a key component of most pain-self management interventions and is intended to address self-regulation. All patients can continue to use other pain management strategies ("usual care") in order to mimic real-life conditions.
Arm Title
Usual Care
Arm Type
Active Comparator
Arm Description
Half of the recruited patients (anticipated 20) will receive usual care under the control arm of this study. These participants will not receive the intervention.
Intervention Type
Behavioral
Intervention Name(s)
Liver Education About Pain (LEAP)
Intervention Description
The study team plans to recruit patients at UPMC for participation in the Liver Education About Pain (LEAP) intervention program. LEAP is a modular 12-week pain self-management intervention with alternating group and individual sessions. Group sessions allow participants to practice skills, set goals with the group, seek social support, and learn together. Individual sessions serve the purpose of individualizing the program to the needs of the patients. The purpose of the LEAP program is to make pain better, help patients reach their personal goals (things that may be hard to do because of pain), and add to the care patients' medical team is providing.
Intervention Type
Behavioral
Intervention Name(s)
Usual Care
Intervention Description
Patients can continue to use other pain management strategies ("usual care") in order to mimic real-life conditions.
Primary Outcome Measure Information:
Title
Number of participants attending ≥80% of intervention sessions
Description
Attendance will be studied by combining participant completion of follow-up measures and attending ≥80% of intervention sessions.
Time Frame
Approximately 6-12 months start-to-finish
Title
Overall Satisfaction
Description
The primary acceptability outcome will be overall satisfaction with the intervention and will be operationalized using the Client Satisfaction Questionniare-8, an 8-item Likert-based general satisfaction measure that sums to a score of 8 to 32. A total score of ≥24, indicating an average score of "satisfied" across items, in at least 80% of participants will be operationalized as "acceptable."
Time Frame
Approximately 6-12 months start-to-finish

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All participants must be over 18 years of age and fluent in English Must have a diagnosis of cirrhosis Must be receiving care at UPMC hepatology clinics Must have chronic pain lasting at least 3 months Exclusion Criteria: Participants will be excluded if they are younger than 18 years of age or are unable to provide informed consent for any reason Participants will be excluded if they had a prior liver transplantation or have a limited life expectancy of less than 6 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shari S Rogal, MD, MPH
Phone
866-482-7488
Email
rogalss@upmc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Naudia N Jonassaint, MD, MHS
Phone
412-647-5734
Email
jonassaintnl@upmc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shari S Rogal, MD, MPH
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pittsburgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No

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Improving Pain Management and Opioid Safety for Patients With Cirrhosis

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