Literature DB >> 8444623

Specific psychosocial and behavioral outcomes from the systemic lupus erythematosus self-help course.

C J Braden1, K McGlone, F Pennington.   

Abstract

This study tested hypotheses about the consistency of specified outcomes with strength of program treatment indexed by time spent in a given activity in the Systemic Lupus Erythematosus Self-Help (SLESH) course. Participants had significant increases in enabling skills and in use of relaxation and exercise activities. Participants also had significantly less depression. Consistency between amount of time spent in class and significant changes over time was demonstrated by analysis of treatment strength-response for perception of limitations, depression, enabling skill and for use of rest, relaxation, heat, and exercise activities.

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Mesh:

Year:  1993        PMID: 8444623     DOI: 10.1177/109019819302000105

Source DB:  PubMed          Journal:  Health Educ Q        ISSN: 0195-8402


  9 in total

1.  "Joining the dots" for patients with systemic lupus erythematosus: personal perspectives of health care from a qualitative study.

Authors:  E D Hale; G J Treharne; A C Lyons; Y Norton; S Mole; D L Mitton; K M J Douglas; N Erb; G D Kitas
Journal:  Ann Rheum Dis       Date:  2005-10-11       Impact factor: 19.103

2.  Improvement of coping abilities in patients with systemic lupus erythematosus: a prospective study.

Authors:  M Haupt; S Millen; M Jänner; D Falagan; R Fischer-Betz; M Schneider
Journal:  Ann Rheum Dis       Date:  2005-04-13       Impact factor: 19.103

Review 3.  Effective Self-Management Interventions for Patients With Lupus: Potential Impact of Peer Mentoring.

Authors:  Edith M Williams; Leonard Egede; Trevor Faith; James Oates
Journal:  Am J Med Sci       Date:  2017-02-03       Impact factor: 2.378

4.  Become your own advocate: advice from women living with scleroderma.

Authors:  Cindy Mendelson; Janet L Poole
Journal:  Disabil Rehabil       Date:  2007-10-15       Impact factor: 3.033

Review 5.  Self-efficacy and arthritis disability: An updated synthesis of the evidence base and its relevance to optimal patient care.

Authors:  Ray Marks
Journal:  Health Psychol Open       Date:  2014-12-23

6.  Health service utilization among African American women living with systemic lupus erythematosus: perceived impacts of a self-management intervention.

Authors:  Abena A Twumasi; Anna Shao; Charmayne Dunlop-Thomas; Cristina Drenkard; Hannah L F Cooper
Journal:  Arthritis Res Ther       Date:  2019-06-25       Impact factor: 5.156

7.  'More extraordinary than mundane … ' A phenomenological analysis of the experiences of individuals living with CLE and their taking care in the sun.

Authors:  Bláithín McGarry; Donal O'Kane; Collette McCourt; Gerard J Gormley
Journal:  Lupus       Date:  2020-09-17       Impact factor: 2.911

8.  Support Methodologies for African American Women With Lupus - Comparing Three Methods' Effects on Patient Activation and Coping.

Authors:  Ashley White; Trevor D Faith; Aissatou Ba; Aundrea Loftley; Viswanathan Ramakrishnan; Hetlena Johnson; Jillian Rose; Clara L Dismuke-Greer; Jim C Oates; Leonard E Egede; Edith M Williams
Journal:  Front Psychol       Date:  2021-10-05

9.  Elevated Salivary Alpha-Amylase Level, Association Between Depression and Disease Activity, and Stress as a Predictor of Disease Flare in Systemic Lupus Erythematosus: A Prospective Case-Control Study.

Authors:  Ju-Yang Jung; Jin-Young Nam; Hyoun-Ah Kim; Chang-Hee Suh
Journal:  Medicine (Baltimore)       Date:  2015-07       Impact factor: 1.889

  9 in total

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