Abstract

BackgroundAlopecia Areata (AA) is an autoimmune disease that is characterised by hair loss. Individuals diagnosed with it often describe feelings of trauma and social rejection due to cosmetic repercussions and are at high risk of experiencing psychological distress. Physical activity (PA) participation has been associated with better mental health outcomes in diverse populations. A preliminary study of individuals with AA indicated that severe hair loss is associated with symptomatic depression, anxiety and stress, which negatively impacted PA participation. While strategies to increase PA participation in the general population have been established, little is known about PA participation in people with AA. This study aimed to understand barriers and enablers to PA participation in people with AA to inform the development of evidence-based interventions.MethodsThe study used a grounded theory (GT) methodology, relying on an iterative and simultaneous process of data collection, coding, theory development, and data comparisons to explore the perceived barriers and enablers to PA. Data were collected through a focus group (8 participants [33.38 ± 10.81 years]) and individual telephone interviews (8 participants [33.89 ± 11.87 years]). The study was conducted in Melbourne, Australia. Interview data were recorded digitally, transcribed verbatim and analysed. Recruitment continued until theoretical saturation was achieved.ResultsThe constructivist grounded theory method used has assisted to develop an explanatory model which is used to explain the themes for barriers and enablers to PA participation. The four phases in the explanatory model are as follows (1) onset of AA; (2) reaction towards the condition; (3) adjustment; and (4) acceptance.ConclusionThe findings highlighted perceived barriers and enablers to PA participation in people with AA. Future interventions could consider addressing these barriers specifically to maximise effectiveness and to improve mental health status based on the phases of the explanatory model.

Highlights

  • Alopecia Areata (AA) is an autoimmune-mediated disease that causes non-scarring hair loss with a prevalence of 0.1–0.2% and lifetime incidence of 2.1% [1]

  • Full list of author information is available at the end of the article

  • Individuals with AA were recruited through advertisements on the websites of the Australia Alopecia Areata Foundation (AAAF) and its social media page

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Summary

Introduction

Alopecia Areata (AA) is an autoimmune-mediated disease that causes non-scarring hair loss with a prevalence of 0.1–0.2% and lifetime incidence of 2.1% [1]. There are numerous treatment options available, but the effects of these on hair loss are typically short-term, which, in turn, negatively affects the emotions and mental health of people with AA [4, 5]. The psychological effects of such practices are complex; concealing hair loss can increase self‐confidence, but concerns about wigs being noticed or coming off can simultaneously increase anxiety and stress, create feelings of inauthenticity and affect interactions with others, leading to avoidance of social activities those involving physical activity [8, 9]. Alopecia Areata (AA) is an autoimmune disease that is characterised by hair loss Individuals diagnosed with it often describe feelings of trauma and social rejection due to cosmetic repercussions and are at high risk of experiencing psychological distress. This study aimed to understand barriers and enablers to PA participation in people with AA to inform the development of evidence-based interventions

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