- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05652608
Stronger Together Psoriatic Arthritis Wellness Study
Patients diagnosed with psoriatic arthritis (PsA) confront decisions about how to treat their disease, interact with their health care providers, and modify lifestyle choices that may improve treatment outcomes. With sponsorship support from Janssen and in partnership with the Cleveland Clinic, this survey study will seek to understand and examine whether people living with PsA are interested in and motivated to participate in wellness activities. This cross-sectional observational survey study will help researchers and clinicians to better understand what some of the barriers and facilitators experienced by patients are when considering participation in guided online wellness activities.
People that qualify for the study and complete a 10-minute survey will be invited to participate in Immune Strength, an online wellness program developed by the Cleveland Clinic. Immune Strength is a free 10-week program for creating better habits for a more resilient immune system. By following this program, participants will have the opportunity to learn about how to develop strategies and implement behavior changes for healthier immune functioning.
Participants will be recruited by the Global Healthy Living Foundation (GHLF). GHLF is the parent organization of the CreakyJoints® (CJ) arthritis patient community and primary site for the PCORI-funded Arthritis Patient Partnership with Comparative Effectiveness Researchers (AR-PoWER) Patient Powered Research Network (PPRN), known as ArthritisPower®. ArthritisPower is a subset of CreakyJoints members who have expressed interest in participating in research and signed an informed consent form to participate in the PPRN and its associated research. Any individuals recruited from CreakyJoints or Facebook, who are not already members of ArthritisPower will be encouraged to join the ArthritisPower registry research app, but will not be required to do so in order to participate in the study.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Shilpa Venkatachalam, Phd
- Phone Number: (845) 348 0400
- Email: svenky@ghlf.org
Study Contact Backup
- Name: Laura Stradford, MPH
- Phone Number: (845) 348 0400
- Email: lstradford@ghlf.org
Study Locations
-
-
New York
-
Upper Nyack, New York, United States, 10960
- Recruiting
- Global Healthy Living Foundation
-
Contact:
- Shilpa Venkatachalam, Phd
- Phone Number: (845) 348 0400
- Email: svenky@ghlf.org
-
Contact:
- Ben Nowell, Phd
- Phone Number: 845-348-0400
- Email: bnowell@ghlf.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Participants must be residents of the United States and United States territories
- Participants must be age 19 and above for United States resident or 21 and above for Puerto Rico residents
- Participants must have a self-reported diagnosis of psoriatic arthritis (PsA) (as indicated by survey screening questions)
- Participants must be taking prescribed medication to treat their PsA
- Participants must have access to a computer or smartphone to take the survey
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Particpants
participating in Immune Strength, a multi-week wellness program
|
Multi-week wellness program provided by the Cleveland Clinic
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Barriers to Wellness
Time Frame: Day 1
|
Percent of participants that experience barriers in using wellness to help manage their disease
|
Day 1
|
|
Interest in Wellness Programs
Time Frame: Day 1
|
Percent of participants interested in participating in a wellness program to complement treatment for controlling their disease
|
Day 1
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pro00062932
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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