Crowdsourcing for Research Data Collection in Rosacea

Overview

Journal Dermatol Online J

Specialty Dermatology

Date 2012 Apr 10

PMID 22483526

Citations 4

Authors

April W Armstrong

Caitlin T Harskamp

Safia Cheeney

Clayton W Schupp

Affiliations

Soon will be listed here.

Abstract

Several medical crowdsourcing sites are available to patients online, but few studies in the literature have compared crowdsourced data to clinical trials. Herein, we compare data from rosacea patients from a major medical crowdsourcing site with those from randomized controlled trials.

Citing Articles

Clinical manifestations and quality of life in hidradenitis suppurativa patients: survey of participants from an internet support group.

Tavora I, Bissoli G, Miot H, Schmitt J An Bras Dermatol. 2019; 94(3):298-303.

PMID: 31365658 PMC: 6668954. DOI: 10.1590/abd1806-4841.20197687.

Building a Citizen Pscientist: Advancing Patient-Centered Psoriasis Research by Empowering Patients as Contributors and Analysts.

Sanchez I, Shankle L, Wan M, Afifi L, Wu J, Doris F Dermatol Ther (Heidelb). 2018; 8(3):405-423.

PMID: 29876724 PMC: 6109031. DOI: 10.1007/s13555-018-0242-5.

Mapping of Crowdsourcing in Health: Systematic Review.

Crequit P, Mansouri G, Benchoufi M, Vivot A, Ravaud P J Med Internet Res. 2018; 20(5):e187.

PMID: 29764795 PMC: 5974463. DOI: 10.2196/jmir.9330.

Skin self-examinations and visual identification of atypical nevi: comparing individual and crowdsourcing approaches.

King A, Gehl R, Grossman D, Jensen J Cancer Epidemiol. 2013; 37(6):979-84.

PMID: 24075797 PMC: 3849386. DOI: 10.1016/j.canep.2013.09.004.