Barriers to Care and QOL for CCCA Patients

Completed

• Conditions: Central Centrifugal Cicatricial Alopecia; Scarring Alopecia; Central Centrifugal Scarring Alopecia

• Registration Number: NCT03044782
• Lead Sponsor: Northwestern University

Brief Summary

The purpose of the current project is twofold; first to determine what personal, historical, logistical, and environmental factors preclude women from obtaining medical care for CCCA hair loss. Because damage from CCCA is irreversible, early identification and treatment is paramount to limiting the negative ramifications of the disease. Second, to investigate how CCCA hair loss, a common occurrence in the Black population, can be a significant psychological impediment to lives of affected Black women. Based on previous research on the psychosocial impact of generalized hair loss in Black women, it is fair to consider that CCCA hair loss also leads to problems with self-esteem and participation in daily life activities. This research, the first of its kind, will add to existing knowledge of CCCA by investigating the quality of life and barriers to care of patients with this condition. The goal of this study is to illuminate what stands in the way of secondary and tertiary prevention of CCCA patients and tailor treatment strategies to address their needs. The results of this study will be instrumental in modifying dermatology resident training, adding to existing dermatology management guidelines, and even developing public health advocacy programming.

Detailed Description

Not available

Study Timeline

• Study Start: 2016-08
• Study First Submitted: 2016-12-16
• Study First Submitted QC: 2017-02-03
• Study First Posted: 2017-02-07
• Primary Completion: 2017-09
• Study Completion: 2017-09
• Status Verified: 2017-12
• Last Update Submitted: 2017-12-12
• Last Update Posted: 2017-12-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

• Evaluated in the Northwestern Dermatology Department between October 1, 2015 and September 30, 2017.
• Evaluated by any faculty physician.
• Diagnosed with CCCA.
• Age 18 or older.
• All subjects must have given signed informed consent prior to participation in study.

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Exclusion Criteria

• Non-English speakers (interpreters not available)

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Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quantified Quality of Life Survey Responses	Duration of study-approximately 2 years
Quantified Barriers to Care Survey Responses	Duration of study-approximately 2 years

Trial Locations

Locations (1)

Northwestern University Department of Dermatology; 🇺🇸 Chicago, Illinois, United States