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Black Patients' Lived Experiences and Perceptions of Skin of Color Clinics

Black Patients' Lived Experiences and Perceptions of Skin of Color Clinics

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02375659
Enrollment
19
Registered
2015-03-02
Start date
2015-02-28
Completion date
2017-09-30
Last updated
2017-10-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Perception of Skin of Color Clinics in African Americans

Brief summary

Across the U.S. Skin of Color (SOC) clinics have been established with the goal of providing medical care and supporting research related to patients with skin of color. There have been no formal studies evaluating why patients seek medical care at SOC clinics or treatment outcomes. Reasons may include past experiences with other providers, the perception that providers working in these clinics have a special interest or knowledge in caring for patients with skin of color and thus may provide better care, the expectation of cultural sensitivity, the hope that their provider may have a similar ethnic background, and/or ease of communication with their provider. Through focus group discussions we aim to identify the factors influencing a patient's choice to seek medical care at a SOC clinic and to gain insight into the presence and impact of racial concordance between provider and patient. The current study will focus on self-identified African American patients with interest in conducting similar sessions with patients of other ethnicities and races in the future.

Interventions

None listed

Sponsors

University of Wisconsin, Stout
CollaboratorOTHER
Northwestern University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Evaluated in the Northwestern Center for Ethnic Skin between February 1, 2015 and February 1, 2016. * Evaluated by Drs. Stavonnie Patterson or Roopal Kundu * Age 18 or older * Self identified as African American/Black * All subjects must have given signed, informed consent prior to participation in study.

Exclusion criteria

* English speaking as interpreters not available * Existing mental health conditions that may interfere with focus group discussion

Design outcomes

Primary

MeasureTime frameDescription
Common thematic responses of discussion groups100 minutesAudiotapes of focus group discussions will be transcribed, and the transcripts will be analyzed via a 'long-hand' inductive approach by two dermatologists and one psychologist. For each of the 8 posed focus group questions, the reviewers will independently induce a common thematic response. Collectively, they will then compare their independently derived themes, identifying themes of agreement and disagreement. Areas of disagreement will be further reviewed until a mutually agreed upon final set of themes is identified. The raw data corresponding to the item in question will be classified according to its theme.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026