Literature DB >> 26599674

Gender differences in caregiver strain, needs for support, social support, and quality of life among spousal caregivers of persons with multiple sclerosis.

Eun-Jeong Lee1, Jessica Pieczynski1, Samantha DeDios-Stern1, Camille Simonetti2, Gloria K Lee3.   

Abstract

BACKGROUND: Caregivers of individuals with MS may experience unique caregiver strain due to the age at onset and progressive nature of the disease. Additionally, because MS is more prevalent in women, men often become spousal caregivers. However, gender differences in psychosocial adjustment among caregivers have not been fully explored.
OBJECTIVE: The purpose of this study was to explore gender differences in the need for various supports and type of social support needed, caregiver strain, and quality of life among caregivers for individuals with MS.
METHODS: 106 caregivers participated in this study. Independent sample t-tests and multiple regression analyses were conducted to examine gender differences in strain, need for supports, social support, and quality of life.
RESULTS: Analyses revealed gender difference among important psychosocial variables. Specifically, women reported higher levels of caregiver strain, higher needs for emotional support, and higher perceived social support. Additionally, multiple regression analyses revealed an inverse relationship between expressed emotional needs and quality of life for men, but not for women.
CONCLUSIONS: MS caregivers experience significant strain that diminishes quality of life. Social support and needs fulfillment can act to buffer this stress; however, results indicate that this varies by gender, with gender differences observed in strain, perceived support, and expressed needs among MS caregivers. The study implications for rehabilitation research are discussed.

Entities:  

Keywords:  Caregiving; gender differences; multiple sclerosis

Mesh:

Year:  2015        PMID: 26599674     DOI: 10.3233/WOR-152205

Source DB:  PubMed          Journal:  Work        ISSN: 1051-9815


  4 in total

1.  Perceptions of parents of the impact of autism spectrum disorder on their quality of life and correlates: comparison between mothers and fathers.

Authors:  Christelle Vernhet; Cécile Michelon; Florine Dellapiazza; Cécile Rattaz; Marie-Maude Geoffray; Herbert Roeyers; Marie-Christine Picot; Amaria Baghdadli
Journal:  Qual Life Res       Date:  2021-11-25       Impact factor: 4.147

Review 2.  Caregiver Burden in Multiple Sclerosis: Recent Trends and Future Directions.

Authors:  Rebecca Maguire; Phil Maguire
Journal:  Curr Neurol Neurosci Rep       Date:  2020-05-22       Impact factor: 5.081

3.  Preferences for Using a Mobile App in Sickle Cell Disease Self-management: Descriptive Qualitative Study.

Authors:  Tilicia L Mayo-Gamble; Delores Quasie-Woode; Jennifer Cunningham-Erves; Margo Rollins; David Schlundt; Kemberlee Bonnet; Velma McBride Murry
Journal:  JMIR Form Res       Date:  2021-11-30

4.  State anxiety, uncertainty in illness, and needs of family members of critically ill patients and their experiences with family-centered multidisciplinary rounds: A mixed model study.

Authors:  Jiyeon Kang; Young-Jae Cho; Seunghye Choi
Journal:  PLoS One       Date:  2020-06-09       Impact factor: 3.240

  4 in total

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