Literature DB >> 24240060

A multicentre postal survey investigating the contribution of illness perceptions, coping and optimism to quality of life and mood in adults with muscle disease.

Christopher D Graham1, John Weinman, Reza Sadjadi, Trudie Chalder, Richard Petty, Mike G Hanna, Chris Turner, Matt Parton, Paul Maddison, Aleksandar Radunovic, Cheryl Longman, Yvonne Robb, Kate Bushby, David Hilton-Jones, Michael R Rose.   

Abstract

OBJECTIVE: To replicate the finding that illness perceptions influence quality of life in adults with muscle disease and to explore the additional influence of coping and optimism on quality of life and mood.
DESIGN: A postal survey including questionnaires recording quality of life, mood, illness perceptions, optimism, coping and functional impairment.
SETTING: National Health Service muscle clinics in the United Kingdom. PARTICIPANTS: A convenience sample of adults with muscle disease.
INTERVENTIONS: Not applicable. MAIN OUTCOME MEASURES: Individualised Neuromuscular Quality of Life Questionnaire, Hospital Anxiety and Depression Scale.
RESULTS: A total of 226 completed questionnaires were returned. Although functional impairment explained most of the variance in three out of eight quality of life domains, psychological factors explained greater amounts of variance (between 19% and 52% of variance) in all other quality of life domains and in both mood domains (between 45% and 48% of variance). Overall, illness perceptions explained much of the variance in quality of life and mood score (between 5% and 37% of variance), while coping (up to 8% of variance) and optimism (up to 15% of variance) explained smaller amounts of variance.
CONCLUSION: The results confirm that illness perceptions are associated with quality of life in muscle disease and suggest that they also influence mood. The addition of optimism and coping variables into the analysis yielded small increases in the proportions of variance in quality of life and mood which were explained. These results have implications for the composition of future psychological interventions.

Entities:  

Keywords:  Coping; illness perceptions; mood; muscle disease; muscular diseases; neuromuscular; quality of life

Mesh:

Year:  2013        PMID: 24240060     DOI: 10.1177/0269215513511340

Source DB:  PubMed          Journal:  Clin Rehabil        ISSN: 0269-2155            Impact factor:   3.477


  12 in total

1.  Quality of life of persons living with HIV and congruence with surrogate decision-makers.

Authors:  Katherine B Curtin; Yao I Cheng; Jichuan Wang; Rachel K Scott; Leah Squires; Debra A Benator; Maureen E Lyon
Journal:  Qual Life Res       Date:  2018-09-15       Impact factor: 4.147

2.  Contribution of the self-regulation model to understanding the health related quality of life of rheumatoid arthritis patients.

Authors:  Shiri Shinan-Altman; Shiran Afuta-Goldstein
Journal:  Qual Life Res       Date:  2019-10-01       Impact factor: 4.147

3.  Assessing the affective load in the narratives of women suffering from fibromyalgia: the clinicians' appraisal.

Authors:  Christine Cedraschi; Elodie Girard; Valérie Piguet; Jules Desmeules; Anne-Françoise Allaz
Journal:  Health Expect       Date:  2014-12-10       Impact factor: 3.377

4.  The relationship between physical symptoms and health-related quality of life in oculopharyngeal muscular dystrophy.

Authors:  Sarah Youssof
Journal:  Muscle Nerve       Date:  2016-03-01       Impact factor: 3.217

5.  Health-related quality of life in multiple sclerosis: role of cognitive appraisals of self, illness and treatment.

Authors:  Maciej Wilski; Tomasz Tasiemski
Journal:  Qual Life Res       Date:  2015-12-16       Impact factor: 4.147

6.  The facioscapulohumeral muscular dystrophy Rasch-built overall disability scale (FSHD-RODS).

Authors:  Karlien Mul; Tatiana Hamadeh; Corinne G C Horlings; Rabi Tawil; Jeffrey M Statland; Sabrina Sacconi; Alastair J Corbett; Nicol C Voermans; Catharina G Faber; Baziel G M van Engelen; Ingemar S J Merkies
Journal:  Eur J Neurol       Date:  2021-05-02       Impact factor: 6.089

7.  Psychological approach in managing muscular dystrophy patients in malaysia.

Authors:  Elna Herawati Che Ismail; Nooraini Othman
Journal:  Iran J Public Health       Date:  2015-03       Impact factor: 1.429

Review 8.  Do Psychosocial Interventions Improve Quality of Life and Wellbeing in Adults with Neuromuscular Disorders? A Systematic Review and Narrative Synthesis.

Authors:  Elaine Walklet; Kate Muse; Jane Meyrick; Tim Moss
Journal:  J Neuromuscul Dis       Date:  2016-08-30

9.  A blended psychosocial support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: protocol of a randomized controlled trial.

Authors:  Jessica de Wit; Anita Beelen; Constance H C Drossaert; Ruud Kolijn; Leonard H van den Berg; Johanna M A Visser-Meily; Carin D Schröder
Journal:  BMC Psychol       Date:  2018-05-02

10.  Acceptance and Commitment Therapy for Muscle Disease (ACTMus): protocol for a two-arm randomised controlled trial of a brief guided self-help ACT programme for improving quality of life in people with muscle diseases.

Authors:  Michael R Rose; Sam Norton; Chiara Vari; Victoria Edwards; Lance McCracken; Christopher D Graham; Aleksandar Radunovic; Trudie Chalder
Journal:  BMJ Open       Date:  2018-10-03       Impact factor: 2.692

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