Use of Telemedicine to Address 'Off Target' Symptoms in Psoriatic Arthritis (PsA): Implementation of PsOWellTM in PsA

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This will be a single-arm interventional study to test the acceptability, feasibility, and effectiveness of structured telemedicine visits to encourage lifestyle changes that will improve quality of life, disease impact, and disease activity in patients with psoriatic arthritis (PsA).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 89
Healthy Volunteers: f
View:

• Population: Patients with Psoriatic Arthritis

‣ Age 18-89.

⁃ Active symptoms of PsA as defined by a PsA Impact of Disease (PsAID) questionnaire score \>4 (range 0-10, 4 is the patient acceptable symptom state) or a patient global assessment of greater than 4 (scale 0-10).

⁃ Patients should be stable on therapy (i.e., not planning to switch therapy at the current visit).

⁃ Meet CASPAR criteria.

⁃ Provision of signed and dated informed consent form.

⁃ Willingness to comply with all study procedures and availability for duration of the study.

⁃ Has access to a mobile phone or other mobile device.

Locations
United States
Pennsylvania
University Of Pennsylvania
RECRUITING
Philadelphia
Utah
University of Utah
RECRUITING
Salt Lake City
Contact Information
Primary
Sarah Hopkins Gillespie
Sarah.Hopkins@Pennmedicine.upenn.edu
(215) 614-1840
Backup
Study Coordinator
SpAProgram@pennmedicine.upenn.edu
Time Frame
Start Date: 2023-03-10
Estimated Completion Date: 2025-12
Participants
Target number of participants: 87
Treatments
Experimental: Interventional Telemedicine Arm
Single Arm Intervention
Related Therapeutic Areas
Sponsors
Leads: University of Pennsylvania

This content was sourced from clinicaltrials.gov