28 citations
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January 2015 in “Journal der Deutschen Dermatologischen Gesellschaft” This study found that Greek adult women with scarring alopecia experience more significant psychological burden and quality of life impairment compared to those with non-scarring alopecia.
October 2025 in “JDDG Journal der Deutschen Dermatologischen Gesellschaft” Hair loss negatively impacts quality of life, and psychological support can help.
March 2026 in “Clinical and Experimental Dermatology” This study found that patients with chronic, persistent alopecia areata experience significant psychosocial impairments unrelated to scalp hair loss, which influence their decision to start systemic therapy.
April 2026 in “Clinical and Experimental Dermatology” The authors concluded that for alopecia areata, addressing psychosocial well-being and social functioning is crucial, as the burden of the condition extends beyond visible hair loss and includes substantial inequities in treatment access.
January 2026 in “British Journal of Health Psychology” This review highlights the significant impact of alopecia on personal identity and social interactions, emphasizing the need for personalized, non-pharmacological interventions and improved collaboration in healthcare training to better support those with appearance-altering conditions.
