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NCT06264492 Clinical Trial

Delving Into Participation Trends of Scleroderma Clinical Trials

Scleroderma Clinical Trial

Official title:
Deciphering Patient Participation: Insights From Observational Data in Scleroderma Clinical Trials

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06264492
Other study ID # 55777205
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 2025
Est. completion date March 2027

Study information
Verified date February 2024
Source Power Life Sciences Inc.
Contact Michael B Gill
Phone 4159004227
Email bask@withpower.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Typically, specific demographic subsets tend to exhibit greater engagement in medical research. Nonetheless, there is insufficient research elucidating the trial characteristics influencing the participation of these particular demographics. The study will analyze data from diverse demographic viewpoints to uncover recurring trends that could provide valuable insights for future patients with scleroderma.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 500
Est. completion date March 2027
Est. primary completion date March 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patient has been diagnosed with scleroderma - Patient has self-identified as planning to enroll in an observational clinical trial - Patient is a minimum of 18 years or older Exclusion Criteria: - Patient is pregnant - Inability to perform regular electronic reporting - Patient does not understand, sign, and return consent form

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Power Life Sciences San Francisco California

Sponsors (1)
Lead Sponsor Collaborator
Power Life Sciences Inc.

Country where clinical trial is conducted

United States, 

References & Publications (3)

Careta MF, Leite Cda C, Cresta F, Albino J, Tsunami M, Romiti R. Prospective study to evaluate the clinical and radiological outcome of patients with scleroderma of the face. Autoimmun Rev. 2013 Sep;12(11):1064-9. doi: 10.1016/j.autrev.2013.05.005. Epub 2013 Jun 19. — View Citation

Harb S, Pelaez S, Carrier ME, Kwakkenbos L, Bartlett SJ, Hudson M, Mouthon L, Sauve M, Welling J, Shrier I, Thombs BD; SPIN Physical Activity Enhancement Patient Advisory Team and SPIN Investigators. Barriers and Facilitators to Physical Activity for People With Scleroderma: A Scleroderma Patient-Centered Intervention Network Cohort Study. Arthritis Care Res (Hoboken). 2022 Aug;74(8):1300-1310. doi: 10.1002/acr.24567. Epub 2022 May 11. — View Citation

Li SC. Treatment of juvenile localized scleroderma: current recommendations, response factors, and potential alternative treatments. Curr Opin Rheumatol. 2022 Sep 1;34(5):245-254. doi: 10.1097/BOR.0000000000000886. — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of patients in clinical research for scleroderma 3 months
Primary Number of scleroderma study participants who stay committed until clinical study wraps up 12 months
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