Literature DB >> 28512762

Importance of Group Therapeutic Support for Family Members of Children with Alopecia Areata: A Cross-Sectional Survey Study.

Kelly A Aschenbeck1, Sarah L McFarland1, Maria K Hordinsky2, Bruce R Lindgren3, Ronda S Farah2.   

Abstract

BACKGROUND/
OBJECTIVES: The psychological effect of alopecia areata (AA) is well documented, but group interaction may help lessen this burden. We aimed to determine factors that draw patients with AA and their families to group events.
METHODS: Surveys were administered at the annual alopecia areata bowling social in 2015 and 2016. This event is a unique opportunity for children with AA and their families to meet others with the disease and connect with local support group resources from the Minnesota branch of the National Alopecia Areata Foundation. Data from 2015 and 2016 were combined. Comparisons of subgroups were performed using Fisher exact tests for response frequencies and percentages and two-sample t tests for mean values.
RESULTS: An equal number of men and women participated in the study (n = 13 each). The average age was 41.1 years. There were no significant differences (p > 0.05) in survey responses based on respondent age or sex. Twenty-three (88.5%) attendees sought to connect with others with AA and met three or more people during the event. Seventeen (65.4%) also attended other support group events. Twelve respondents (46.2%) came to support a friend or family member. One hundred percent of attendees identified socializing with others with AA as important.
CONCLUSIONS: Group interaction is an important source of therapeutic support for people with AA and their families.
© 2017 Wiley Periodicals, Inc.

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Year:  2017        PMID: 28512762      PMCID: PMC5813807          DOI: 10.1111/pde.13176

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  11 in total

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Review 2.  The psychological impact of alopecia.

Authors:  Nigel Hunt; Sue McHale
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4.  Attitudes and perceptions of school-aged children toward alopecia areata.

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Review 5.  Alopecia areata: Part 2: treatment.

Authors:  Frank Spano; Jeff C Donovan
Journal:  Can Fam Physician       Date:  2015-09       Impact factor: 3.275

6.  Psychological status of patients with alopecia areata.

Authors:  Stefania Alfani; Valeria Antinone; Aurelia Mozzetta; Cristina Di Pietro; Cinzia Mazzanti; Piero Stella; Desanka Raskovich; Damiano Abeni
Journal:  Acta Derm Venereol       Date:  2012-05       Impact factor: 4.437

7.  Psychiatric symptomatology and health-related quality of life in children and adolescents with alopecia areata.

Authors:  Ö Bilgiç; A Bilgiç; K Bahalı; A G Bahali; A Gürkan; S Yılmaz
Journal:  J Eur Acad Dermatol Venereol       Date:  2013-11-16       Impact factor: 6.166

8.  Alopecia areata: psychiatric comorbidity and adjustment to illness.

Authors:  Sergio Ruiz-Doblado; Ana Carrizosa; Maria Jose García-Hernández
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Review 9.  Bald is beautiful?: the psychosocial impact of alopecia areata.

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Journal:  J Health Psychol       Date:  2009-01

10.  Quality of life in alopecia areata: a case-control study.

Authors:  Taciana Rocha de Hollanda; Celso Tavares Sodré; Marco Antonio Brasil; Marcia Ramos-E-Silva
Journal:  Int J Trichology       Date:  2014-01
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2.  Patient Perspectives of the Social, Emotional and Functional Impact of Alopecia Areata: A Systematic Literature Review.

Authors:  Arash Mostaghimi; Lynne Napatalung; Vanja Sikirica; Randall Winnette; Jason Xenakis; Samuel H Zwillich; Boris Gorsh
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3.  Psychosocial and psychiatric comorbidities and health-related quality of life in alopecia areata: A systematic review.

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  3 in total

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