Literature DB >> 16776403

Responses to the acquisition and use of power mobility by individuals who have multiple sclerosis and their families.

Terri M Boss1, Marcia Finlayson.   

Abstract

PURPOSE: To develop an understanding of family members' reactions to the acquisition of power mobility by persons with multiple sclerosis (MS) from the perspectives of the end users and their family members.
METHODS: Data were obtained through semistructured interviews with seven persons with MS using or considering power mobility and four of their family members.
RESULTS: Three major themes emerged from the data. Recognizing the Need for Power Mobility resulted from the interaction between multiple sclerosis progression and the participants' desired performance. Family decision making and communication, insurance funding and approval, and the physical and social environment were just some of the factors affecting the process of Deciding and Obtaining the Power Mobility. Using Power Mobility resulted in positive, negative, and neutral outcomes.
CONCLUSIONS: This study uncovered an overall lack of resources and some issues within the family environment, such as communication and decision making, both of which can negatively impact the acquisition and use of power mobility for persons with MS. Understanding these challenges may assist occupational therapists to facilitate this transition with their clients.

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Mesh:

Year:  2006        PMID: 16776403     DOI: 10.5014/ajot.60.3.348

Source DB:  PubMed          Journal:  Am J Occup Ther        ISSN: 0272-9490


  4 in total

Review 1.  How assistive technology use by individuals with disabilities impacts their caregivers: a systematic review of the research evidence.

Authors:  W Ben Mortenson; Louise Demers; Marcus J Fuhrer; Jeffrey W Jutai; James Lenker; Frank DeRuyter
Journal:  Am J Phys Med Rehabil       Date:  2012-11       Impact factor: 2.159

2.  Psychometric properties of a Power Mobility Caregiver Assistive Technology Outcome Measure.

Authors:  W Ben Mortenson; Louise Demers; Paula W Rushton; Claudine Auger; François Routhier; William C Miller
Journal:  PLoS One       Date:  2017-06-06       Impact factor: 3.240

3.  Narratives reflecting the lived experiences of people with brain disorders: common psychosocial difficulties and determinants.

Authors:  Sally Hartley; Maggie McArthur; Michaela Coenen; Maria Cabello; Venusia Covelli; Joanna Roszczynska-Michta; Tuuli Pitkänen; Jerome Bickenbach; Alarcos Cieza
Journal:  PLoS One       Date:  2014-05-07       Impact factor: 3.240

Review 4.  Intertwined like a double helix: A meta-synthesis of the qualitative literature examining the experiences of living with someone with multiple sclerosis.

Authors:  Anne Parkinson; Crystal Brunoro; Jack Leayr; Vanessa Fanning; Katrina Chisholm; Janet Drew; Jane Desborough; Christine Phillips
Journal:  Health Expect       Date:  2022-02-04       Impact factor: 3.318

  4 in total

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