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This study found that people with alopecia who worry about not wearing a wig reported higher levels of depression, anxiety, and social anxiety, although wig use increased social confidence for many.

Wearing a wig caused a woman's skin condition to worsen due to pressure from the wig's fasteners.

This paper explores the social challenges individuals with medical hair loss face when using wigs, highlighting the complex identity management involved and the social obligations to disclose wig use to close ones.

This study aimed to identify sociodemographic and clinical factors affecting quality of life in African-American women with central centrifugal cicatricial alopecia, a primary scarring hair loss condition, as existing literature on quality of life specifically for these patients is scarce.

In this study, researchers analyzed dermatologists' treatment practices for alopecia areata across five European countries, finding that topical and intralesional corticosteroids are most commonly prescribed for mild to moderate cases, while severe cases often see increased use of immunosuppressants and wigs.