Psoriatic Arthritis and Psoriasis Treatment Decision Aid

NCT ID: NCT03737045

Last Updated: 2026-02-17

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

Clinical Phase

NA

Total Enrollment

37 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-12-01

Study Completion Date

2025-12-31

Brief Summary

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The purpose of this study is to create and test a patient decision aid that facilitates the shared decision-making process when patients with psoriasis and/or psoriatic arthritis are starting or switching to a new therapy.

Detailed Description

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Prior to the interventional study, we will develop a decision aid using design thinking. In this interventional study, we will implement and test a patient-centered decision aid for therapy selection among patients with psoriasis and/or psoriatic arthritis who are starting or switching to a new medication.

Conditions

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Psoriatic Arthritis Psoriasis

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Patients and providers will use a web-based or paper decision aid. They will not be assigned to specific arms or undergo randomized treatment.
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Participants will have a choice of decision aids (web or paper) and will not be blinded. The study team will be aware of each prototype and decision aid that participants use.

Study Groups

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Decision Aid Testing

Participants will have the opportunity to test the different decision aid prototypes while selecting new treatment/therapy.

Group Type OTHER

Decision Aid

Intervention Type OTHER

Participants will test decision aid prototypes that are designed to assist them in choosing a medication.

Interventions

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Decision Aid

Participants will test decision aid prototypes that are designed to assist them in choosing a medication.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Age 18 years or older
2. Diagnosis of psoriasis (as confirmed by dermatologist) or psoriatic arthritis (as confirmed by rheumatologist)
3. Treated at Penn

In addition to the above, for the observation and implementation phases of the study:
4. Initiation of a new psoriasis or psoriatic arthritis treatment

* Biosimilars that have been approved by the FDA and available on the US market will similarly be eligible for participation
* Patients may be taking other traditional DMARDs.
* A washout period is not required.

Exclusion Criteria

1. Unable to give informed consent
2. Youth, under the age of 18 years
3. Patients without psoriasis or psoriatic arthritis
4. Not being treated at a Penn clinic

In addition to the above, for the observation and implementation phases of the study:
5. Not starting or switching to a new medication
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role collaborator

University of Pennsylvania

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Alexis Ogdie-Beatty, MD

Role: PRINCIPAL_INVESTIGATOR

University of Pennsylvania

Locations

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Hospital at the University of Pennsylvania

Philadelphia, Pennsylvania, United States

Site Status

Countries

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United States

Other Identifiers

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831515

Identifier Type: -

Identifier Source: org_study_id

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