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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03620188
Other study ID # IRB00184580
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 20, 2018
Est. completion date June 30, 2022

Study information

Verified date September 2023
Source Johns Hopkins University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The PaGoPsA study objective is to ascertain if guideline-based psoriatic arthritis clinical care achieves individual patient goals as articulated by patients, and to identify predictors of achieving individual patient goals from psoriatic arthritis treatment.


Description:

Psoriatic arthritis (PsA) is a heterogeneous autoimmune disease that occurs in one in three people with the skin disease psoriasis. PsA can cause arthritis (joint inflammation), enthesitis (tendon and ligament inflammation), sausage digits (swollen entire finger or toe), spondyloarthritis (spinal inflammation). Skin involvement by psoriasis is also highly variable in terms of psoriasis type and location. Through combined skin and musculoskeletal involvement, psoriatic disease has a significant life impact with decrease quality of life including uncomfortable symptoms, ability to participate in life and functioning. Medications used to treat PsA have sometimes an uneven effect on the various PsA manifestations where some are more effective for skin while others more effective for the joints. In this context, clinical care and treatment of PsA is a complex process which balances disease activity with medication risks and benefits as well as patient priorities. Professional PsA treatments guidelines state that PsA treatment goals are disease remission or low disease activity. Several studies to date have shown that physicians tend to overestimate remission and low disease activity in PsA patients when compared to disease activity indices. Also patients and physicians frequently do not align on perceptions of remission or low disease activity. In the proposed study the investigators aim to identify predictors of successful treatment from a patient perspective on a range of disease measures including psoriasis, arthritis, enthesitis, dactylitis, patient reported outcomes, and laboratory assessments which are routinely collected in the clinical care of PsA. Secondary endpoints are to quantify longitudinally how stable a state of treatment success is from a patient perspective, and to define score ranges for disease measurements, including health-related quality of life measures, that correspond to treatment success from a patient perspective. The impact of this research is that the investigators will be able to define parameters predictive of achieving treatment success from a patient perspective, which will then inform goals of care for psoriatic arthritis.


Recruitment information / eligibility

Status Completed
Enrollment 250
Est. completion date June 30, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years to 95 Years
Eligibility Inclusion Criteria: - English speaking/reading adults - Patients of the Johns Hopkins Arthritis Center and/or the Johns Hopkins Psoriatic Arthritis Clinical Program - Followed every 3-4 months for regular psoriatic arthritis clinical care - Meet Classification Criteria for Psoriatic Arthritis (CASPAR) - Able to interact with touch screen computer. Exclusion Criteria: None

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Standard of care
Standard of care in PsA is outline in treatment guidelines as adjustment of therapy every 3 months until goals of treatment are being met. Goals of treatment are defined as remission or low disease activity.

Locations

Country Name City State
United States Johns Hopkins Bayview Baltimore Maryland

Sponsors (2)

Lead Sponsor Collaborator
Johns Hopkins University Amgen

Country where clinical trial is conducted

United States, 

References & Publications (1)

Orbai AM, de Wit M, Mease P, Shea JA, Gossec L, Leung YY, Tillett W, Elmamoun M, Callis Duffin K, Campbell W, Christensen R, Coates L, Dures E, Eder L, FitzGerald O, Gladman D, Goel N, Grieb SD, Hewlett S, Hoejgaard P, Kalyoncu U, Lindsay C, McHugh N, Shea B, Steinkoenig I, Strand V, Ogdie A. International patient and physician consensus on a psoriatic arthritis core outcome set for clinical trials. Ann Rheum Dis. 2017 Apr;76(4):673-680. doi: 10.1136/annrheumdis-2016-210242. Epub 2016 Sep 9. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Predictors of reaching PsA treatment goals/treatment success from a patient perspective. The primary outcome determination is based on the patients' report of whether they are/are not at goal with their PsA treatment. 12-16 weeks
Secondary To define a status of PsA treatment where patient treatment goals have been met. Score ranges that correspond to a status of patients' treatment goals met on a set of PsA outcome measures used in the study, including composite disease activity measures. 52 weeks
Secondary Improvement thresholds (treatment success) that correspond to a patient transition from goals not met to met. Meaningful change values in patients who transition longitudinally from goals not met to goals met. 12-16 weeks
Secondary Worsening thresholds (treatment failure) if transition is from goals met to not met. Meaningful change values in patients who transition longitudinally from goals met to goals not met disease activity categories. 12-16 weeks
Secondary Prevalence of treatment success in guideline -based treatment in psoriatic arthritis from the patients' perspective Prevalence of patients reporting they met PsA treatment goals (successful treatment) from their perspective. 52 weeks
Secondary Stability of a state of treatment goals met at subsequent study visits. Frequency and direction of longitudinal transitions between treatment goals/met not met states: 3 observations/participant. 52 weeks
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