12 citations
,
September 2024 in “Journal of the European Academy of Dermatology and Venereology” This review identified several changeable psychosocial factors, like acceptance, as potential targets for interventions aimed at reducing self-stigma and improving mental health in affected individuals.
1 citations
,
September 2023 in “Journal of the American Academy of Dermatology” This study found that self-stigma is common among alopecia areata patients, with 85% experiencing it to some degree, and that factors like increased social support and illness acceptance correlate with lower stigmatization levels, while helplessness correlates with higher levels.
8 citations
,
June 2023 in “British Journal of Dermatology” This study developed and initially validated the Scale of Alopecia Areata Distress (SAAD), a 41-item tool designed to measure psychosocial distress among US adults with alopecia areata.
December 2016 in “The European health psychologist” This study found that women with polycystic ovary syndrome often experience isolation, helplessness, resilience, and grief, suggesting a need for better support during diagnosis and treatment to improve wellbeing.
July 2022 in “Nigerian journal of medicine : journal of the National Association of Resident Doctors of Nigeria” This study found that androgenetic alopecia significantly impairs quality of life among Nigerian patients, especially in areas like emotions, stigmatization, and self-confidence, highlighting the importance of psychosocial support.
2 citations
,
January 2016 in “Knowledge Commons (Lakehead University)” This study investigates the experiences of women with PCOS to increase understanding, reduce stigma, and enhance education about the syndrome for all women.
1 citations
,
October 2025 in “Colorectal Disease” In this study, cancer patients aged 30 to 50 reported experiencing diagnostic delays, coping through self-advocacy, and facing stigma-related challenges such as alopecia. The authors concluded that improved physician awareness, tailored screening, and addressing stigma are essential for enhancing care for early-onset colorectal cancer patients.
2 citations
,
December 2023 in “JEADV Clinical Practice” In this population-based study, researchers reported that nearly half of Greek adults experienced at least one skin condition in the past year, with significant impacts on quality of life, work decisions, and perceptions of stigmatization.
37 citations
,
January 2010 in “International Journal of Trichology” This study concluded that heredity is associated with hair loss, while lifestyle and stress factors are not significantly related.
8 citations
,
March 2019 in “Progress in Human Geography” This paper explores how hair functions as a geographical lens to redefine the body's borders, influencing perceptions of identity and power.
3 citations
,
May 2010 in “Nursing Standard” This article discusses autoimmune-associated alopecia areata, highlighting its psychological and social impact, but reports no new clinical findings.
1 citations
,
October 2016 in “Journal of medical science and clinical research” This study found that younger male patients with androgenic alopecia experienced greater stigmatization and emotional instability but maintained higher self-assuredness and better overall quality of life compared to older patients.
June 2025 in “Canadian dermatology today.” This study highlights the profound impact of alopecia areata on patients' self-esteem and identity, calling for holistic management that includes medical treatment, mental health support, and camouflage strategies to improve quality of life.
16 citations
,
October 2024 in “Journal of Paediatrics and Child Health” This systematic review highlighted significant psychosocial impacts of alopecia areata in children and adolescents, noting challenges such as reduced self-esteem, emotional distress, and social difficulties. The review underscored the need for further research to understand these effects comprehensively and guide clinical support.
January 2013 in “Digital Repository (National Repository of Grey Literature)” This study explores the social and cultural impacts of hair loss, highlighting that it is perceived as a negative or stigmatizing experience by both women undergoing chemotherapy and men with androgenic alopecia.
1 citations
,
January 2010 Asian women experiencing hair loss often feel embarrassed and unhappy, but hair transplantation can offer natural-looking results and improve their self-confidence.
January 2017 in “Acta dermato-venereologica” The congress showed that psychological therapy can help skin condition patients, social media affects acne stigma, education improves atopic dermatitis, and patient satisfaction in dermatology is high, especially with good doctor engagement.
June 2026 in “Universal Library of Multidisciplinary” This study explores a new therapeutic method called THE YOU TECHNIQUE, which uses performing arts like stand-up comedy to help people with alopecia reduce stigmatization and improve coping strategies, showing promising empirical results in enhancing subjective quality of life.
October 2025 in “Contribuciones a las Ciencias Sociales” In this narrative review, the authors discuss the potential impact of hormone therapy on androgenetic alopecia among transgender individuals, especially transgender men using testosterone, and its adverse effects on emotional well-being and body image within a socially stigmatized population.
October 2024 in “Věda a perspektivy” This study found that permanent makeup, or micropigmentation, effectively masks post-surgical cleft lip scars and corrects lip asymmetry, providing aesthetic and psychological benefits such as improved self-esteem and reduced social anxiety, contributing to better social integration for patients.
40 citations
,
June 2023 in “Dermatology and Therapy” This study found that the emotional impact of alopecia areata is significant, but it may not correlate directly with the extent of hair loss since some individuals adapt to the condition.
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.
68 citations
,
January 2008 in “Seminars in reproductive medicine” This narrative review discusses the impact of polycystic ovary syndrome on women's psychological and sexual well-being, highlighting the potential benefits of interdisciplinary treatments and new interventions to improve life satisfaction and coping, but reports no new results.
February 2024 in “International neuropsychiatric disease journal” In this abstract, the authors provide an overview of the psychological impact of alopecia areata, highlighting how this autoimmune disorder can lead to reduced quality of life, increased anxiety and depression symptoms, and decreased work productivity due to hair loss and its social implications.
June 2013 in “Digital Repository (National Repository of Grey Literature)” This research explores the sociological impact of hair loss, finding that both women and men regard it as a negative experience and employ different strategies to cope with its implications.
23 citations
,
August 2018 in “Anais Brasileiros De Dermatologia” This study found that patients with androgenetic alopecia reported more impact on their quality of life in terms of emotions, functioning, and symptoms than those with alopecia areata.
7 citations
,
July 2019 in “International archives of internal medicine” This review discusses the psychological and emotional effects of common dermatologic conditions and highlights their impact on quality of life, but it does not present new clinical results.
1 citations
,
June 2023 in “Sciential - McMaster Undergraduate Science Journal” This paper reviews scalp cooling as an effective method for preventing chemotherapy-induced alopecia, highlighting recent trials that demonstrate its ability to preserve and regrow hair, thus improving patient well-being.
January 2026 in “Egyptian Journal of Dermatology and Venerology” This study in Egyptian children found that scalp hair loss significantly impacts quality of life, with nearly half experiencing severe emotional and social challenges, particularly those with alopecia areata and tinea capitis.
June 2022 in “Plastic and reconstructive surgery. Global open” This study found that platelet-rich plasma treatment significantly improved patients' quality of life and emotional well-being 3-5 months after treatment for hair loss.