Development of a Patient-Reported Outcome Measure to Assess Symptoms in Patients With Primary Sclerosing Cholangitis (PSC)

NCT ID: NCT02247934

Last Updated: 2016-02-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

26 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-10-31

Study Completion Date

2015-10-31

Brief Summary

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The objectives of this qualitative study are to elicit concepts about symptoms that are important to patients with primary sclerosing cholangitis (PSC), as well as the key impacts of symptoms on patients' day-to-day functioning.

Detailed Description

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In Step I, concept elicitation one-on-one interviews (via telephone or in person) will be conducted. The aims of the concept elicitation interviews are to:

1. Identify the most common symptoms, as well as the most important symptoms, for patients with PSC, and
2. Assess whether these symptoms impact day-to-day functioning

An instrument will be developed based on the symptoms reported and in Step II of the study, the performance of the instrument will be assessed with further interviews.

Conditions

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Primary Sclerosing Cholangitis

Study Design

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Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Concept elicitation interviews (Step I)

Approximately 20 participants will be included.

No interventions assigned to this group

Cognitive interviews (Step II)

Approximately 30 participants will be included.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Confirmed diagnosis of PSC based on liver biopsy or diagnostic imaging, with diagnosis made at least three months prior to screening
* Patient report of PSC symptoms associated with PSC diagnosis
* Able to speak, read, and understand English
* Willing and able to provide written informed consent to participate in the research study

Exclusion Criteria

* Patients with other causes of liver or biliary disease, including viral hepatitis, alcoholic liver disease, primary biliary cirrhosis, and secondary sclerosing cholangitis
* Patient with history of liver cirrhosis
* Patients with history of cholangiocarcinoma
* Patients who have received a liver transplant
* Patients currently enrolled in PSC clinical trials; and
* STEP II ONLY: Enrolled in or participated in Step I of this study (concept elicitation)
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Gilead Sciences

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Rob Myers, MD

Role: STUDY_DIRECTOR

Gilead Sciences

Locations

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University of Colorado Hospital, Denver Health Medical Center

Aurora, Colorado, United States

Site Status

University of Miami Miller School of Medicine - Schiff Center for Liver Diseases

Miami, Florida, United States

Site Status

Evidera

Bethesda, Maryland, United States

Site Status

Duke University Medical Center

Durham, North Carolina, United States

Site Status

Organ Care Research Swedish Medical Center

Seattle, Washington, United States

Site Status

Countries

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United States

Other Identifiers

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A-13601-000

Identifier Type: -

Identifier Source: org_study_id

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