Literature DB >> 15682879

Death of a lifestyle: the effects of social support and healthcare support on the quality of life of persons with fibromyalgia and/or chronic fatigue syndrome.

Nancy Schoofs1, Deborah Bambini, Pamela Ronning, Emily Bielak, Jennie Woehl.   

Abstract

PURPOSE: The purpose of this study was to investigate how social support and healthcare support affect the quality of life of persons with fibromyalgia and chronic fatigue syndrome.
METHOD: A constant comparison method was used for the qualitative portion of the research and descriptive correlational methods were used for the quantitative portion.
CONCLUSION: This mixed design research study suggested that social support, unlike healthcare support, is related to Quality of Life (QOL). It was also evident that subjects suffering from CFS and/or FMS do not experience high levels of social support.

Entities:  

Mesh:

Year:  2004        PMID: 15682879     DOI: 10.1097/00006416-200411000-00005

Source DB:  PubMed          Journal:  Orthop Nurs        ISSN: 0744-6020            Impact factor:   0.913


  23 in total

1.  Impact of invalidation and trust in physicians on health outcomes in fibromyalgia patients.

Authors:  Carroline P Lobo; Andrea R Pfalzgraf; Vincent Giannetti; Gibbs Kanyongo
Journal:  Prim Care Companion CNS Disord       Date:  2014-10-09

2.  Assessment of the relatives or spouses cohabiting with the fibromyalgia patients: is there a link regarding fibromyalgia symptoms, quality of life, general health and psychologic status?

Authors:  Sebnem Koldas Dogan; Yesim Kurtais Aytur; Cem Atbasoglu
Journal:  Rheumatol Int       Date:  2010-03-26       Impact factor: 2.631

3.  Mortality in Patients with Myalgic Encephalomyelitis and Chronic Fatigue Syndrome.

Authors:  Stephanie L McManimen; Andrew R Devendorf; Abigail A Brown; Billie C Moore; James H Moore; Leonard A Jason
Journal:  Fatigue       Date:  2016-10-12

Review 4.  A review and meta-synthesis of qualitative studies on myalgic encephalomyelitis/chronic fatigue syndrome.

Authors:  Valerie R Anderson; Leonard A Jason; Laura E Hlavaty; Nicole Porter; Jacqueline Cudia
Journal:  Patient Educ Couns       Date:  2011-05-14

5.  Loneliness, daily pain, and perceptions of interpersonal events in adults with fibromyalgia.

Authors:  Laurie Dempsey Wolf; Mary C Davis
Journal:  Health Psychol       Date:  2014-09       Impact factor: 4.267

6.  Perceived Fatigue Interference and Depressed Mood: Comparison of Chronic Fatigue Syndrome/Myalgic Encephalomyelitis Patients with Fatigued Breast Cancer Survivors.

Authors:  Daniel L Hall; Michael H Antoni; Emily G Lattie; Devika R Jutagir; Sara J Czaja; Dolores Perdomo; Suzanne C Lechner; Jamie M Stagl; Laura C Bouchard; Lisa M Gudenkauf; Lara Traeger; MaryAnn Fletcher; Nancy G Klimas
Journal:  Fatigue       Date:  2015

7.  Health-related quality of life in women with fibromyalgia: clinical and psychological factors associated.

Authors:  Ricardo Pereira Campos; Maria Isabel Vázquez Rodríguez; Maria Isabel Rodríguez Vázquez
Journal:  Clin Rheumatol       Date:  2011-10-07       Impact factor: 2.980

8.  Patients' and professionals' views on managing fibromyalgia.

Authors:  Erica Briones-Vozmediano; Carmen Vives-Cases; Elena Ronda-Pérez; Diana Gil-González
Journal:  Pain Res Manag       Date:  2013 Jan-Feb       Impact factor: 3.037

9.  Personal resource profiles of individuals with chronic pain: Sociodemographic and pain interference differences.

Authors:  Chung Jung Mun; Mary C Davis; Ivan R Molton; Paul Karoly; Hye Won Suk; Dawn M Ehde; Howard Tennen; Robert D Kerns; Mark P Jensen
Journal:  Rehabil Psychol       Date:  2019-01-28

Review 10.  The expressed needs of people with chronic fatigue syndrome/myalgic encephalomyelitis: a systematic review.

Authors:  Maria de Lourdes Drachler; Jose Carlos de Carvalho Leite; Lee Hooper; Chia Swee Hong; Derek Pheby; Luis Nacul; Eliana Lacerda; Peter Campion; Anne Killett; Maggie McArthur; Fiona Poland
Journal:  BMC Public Health       Date:  2009-12-11       Impact factor: 3.295

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