Literature DB >> 27521652

Enhanced psychological flexibility and improved quality of life in chronic fatigue syndrome/myalgic encephalomyelitis.

Sarah Densham1, Deborah Williams2, Anne Johnson2, Julie M Turner-Cobb3.   

Abstract

OBJECTIVE: Psychological Flexibility (PF) is a relatively new concept in physical health. It can be defined as an overarching process of being able to accept the presence of wanted/unwanted experiences, choosing whether to change or persist in behaviour in response to those experiences. Associations between processes of PF and quality of life (QoL) have been found in long-term health conditions such as chronic pain, PF has not yet been applied to Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME).
METHODS: Changes in PF, fatigue severity and QoL were examined in one hundred and sixty-five patients with CFS/ME engaged in a six-week outpatient interdisciplinary group treatment programme. Participants were assessed using a series of self-report measures at the start of the start (T1) and end of a six-week programme (T2) and at six months follow up (T3).
RESULTS: Significant changes in PF and QoL were observed from pre-treatment (T1) to post treatment follow-up (T2 and T3); changes in fatigue severity were observed from T1 to T3 only. Controlling for fatigue severity, changes in the PF dimension of activity/occupational engagement were associated with improvement in QoL at six month follow up (T3) but not at six weeks post programme (T2).
CONCLUSION: Findings indicate an interdisciplinary group treatment approach for people with CFS/ME may be associated with improved QoL, processes of PF and fatigue severity, supporting a link between PF and long term health conditions. Results highlight links between PF and patient QoL in CFS/ME and the value of interdisciplinary treatment approaches in this patient population.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Acceptance; Chronic fatigue; Interdisciplinary treatment; Psychological flexibility; Quality of life; Values

Mesh:

Year:  2016        PMID: 27521652     DOI: 10.1016/j.jpsychores.2016.07.009

Source DB:  PubMed          Journal:  J Psychosom Res        ISSN: 0022-3999            Impact factor:   3.006


  3 in total

1.  Adult patients' experiences of NHS specialist services for chronic fatigue syndrome (CFS/ME): a qualitative study in England.

Authors:  Jessica Broughton; Sarah Harris; Lucy Beasant; Esther Crawley; Simon M Collin
Journal:  BMC Health Serv Res       Date:  2017-06-02       Impact factor: 2.655

2.  Qualitative study of the acceptability and feasibility of acceptance and commitment therapy for adolescents with chronic fatigue syndrome.

Authors:  Philippa Clery; Jennifer Starbuck; Amanda Laffan; Roxanne Morin Parslow; Catherine Linney; Jamie Leveret; Esther Crawley
Journal:  BMJ Paediatr Open       Date:  2021-10-01

3.  The impact of COVID-19 stress on pain and fatigue in people with and without a central sensitivity syndrome.

Authors:  Tim Y Koppert; Johannes W G Jacobs; Mark A Lumley; Rinie Geenen
Journal:  J Psychosom Res       Date:  2021-10-29       Impact factor: 3.006

  3 in total

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