Literature DB >> 20580520

Finding the right balance of physical activity: a focus group study about experiences among patients with chronic fatigue syndrome.

Lillebeth Larun1, Kirsti Malterud.   

Abstract

OBJECTIVE: To explore contexts of experiences of physical activity perceived as beneficial or harmful for CFS patients.
METHODS: A qualitative study with empirical data from two focus groups with purposive sampling. Mean age was 50, two of ten participants were male, and social demographics varied. Participants were invited to share stories of good as well as bad experiences concerning physical activity. Data were analysed with systematic text condensation.
RESULTS: Participants were not averse to physical activity, but specific preconditions would determine how the activity was perceived. Physical activity was experienced as helpful and enjoyable, especially related to leisure activities where flexible and individual adaptation was feasible. Non-customized activity may precipitate set-backs giving patients the impression of losing control and being betrayed by their bodies. Strategies to review energy usage in daily life could adjust expectations, diminish stress load and assist in approaching a more appropriate priority and balance.
CONCLUSION: Self-management, body awareness and physical activity of choice combined with facilitation and advice from health care professionals is essential to achieve a positive outcome. PRACTICE IMPLICATIONS: Exercise programmes should be adapted, paced, and self-managed in accordance with personal preferences and activity levels to be beneficial and empowering for CFS patients.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Year:  2010        PMID: 20580520     DOI: 10.1016/j.pec.2010.05.027

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  5 in total

1.  To be held and to hold one's own: narratives of embodied transformation in the treatment of long lasting musculoskeletal problems.

Authors:  Randi Sviland; Kari Martinsen; Målfrid Råheim
Journal:  Med Health Care Philos       Date:  2014-11

2.  Social support needs for equity in health and social care: a thematic analysis of experiences of people with chronic fatigue syndrome/myalgic encephalomyelitis.

Authors:  Jose C de Carvalho Leite; Maria de L Drachler; Anne Killett; Swati Kale; Luis Nacul; Maggie McArthur; Chia Swee Hong; Lucy O'Driscoll; Derek Pheby; Peter Campion; Eliana Lacerda; Fiona Poland
Journal:  Int J Equity Health       Date:  2011-11-02

3.  "There are more things in heaven and earth!" How knowledge about traditional healing affects clinical practice: interviews with conventional health personnel.

Authors:  Anette Langås-Larsen; Anita Salamonsen; Agnete Egilsdatter Kristoffersen; Torunn Hamran; Bjørg Evjen; Trine Stub
Journal:  Int J Circumpolar Health       Date:  2017       Impact factor: 1.228

4.  "We own the illness": a qualitative study of networks in two communities with mixed ethnicity in Northern Norway.

Authors:  Anette Langås-Larsen; Anita Salamonsen; Agnete Egilsdatter Kristoffersen; Torunn Hamran; Bjørg Evjen; Trine Stub
Journal:  Int J Circumpolar Health       Date:  2018-12       Impact factor: 1.228

Review 5.  Management of chronic fatigue syndrome/myalgic encephalomyelitis in a pediatric population: A scoping review.

Authors:  Sarah S Collard; Jane Murphy
Journal:  J Child Health Care       Date:  2019-08-04       Impact factor: 1.979

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.