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Taking Charge of Systemic Sclerosis: A Pilot Study to Assess the Effectiveness of an Internet Self‐Management Program
dc.contributor.authorPoole, Janet L.en_US
dc.contributor.authorMendelson, Cindyen_US
dc.contributor.authorSkipper, Bettyen_US
dc.contributor.authorKhanna, Dineshen_US
dc.date.accessioned2014-05-23T15:59:04Z
dc.date.availableWITHHELD_13_MONTHSen_US
dc.date.available2014-05-23T15:59:04Z
dc.date.issued2014-05en_US
dc.identifier.citationPoole, Janet L.; Mendelson, Cindy; Skipper, Betty; Khanna, Dinesh (2014). "Taking Charge of Systemic Sclerosis: A Pilot Study to Assess the Effectiveness of an Internet Self‐Management Program." Arthritis Care & Research 66(5): 778-782.en_US
dc.identifier.issn2151-464Xen_US
dc.identifier.issn2151-4658en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/106842
dc.publisherSage Publicationsen_US
dc.publisherWiley Periodicals, Inc.en_US
dc.titleTaking Charge of Systemic Sclerosis: A Pilot Study to Assess the Effectiveness of an Internet Self‐Management Programen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeriatricsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/106842/1/acr22192.pdf
dc.identifier.doi10.1002/acr.22192en_US
dc.identifier.sourceArthritis Care & Researchen_US
dc.identifier.citedreferenceJoachim G, Acorn S. Life with a rare chronic disease: the scleroderma experience. J Adv Nurs 2003; 42: 598 – 606.en_US
dc.identifier.citedreferenceMendelson C, Poole JL. Become your own advocate: advice from women living with scleroderma. Disabil Rehabil 2007; 29: 1492 – 501.en_US
dc.identifier.citedreferenceRubenzik TT, Derk CT. Unmet patient needs in systemic sclerosis. J Clin Rheumatol 2007; 15: 106 – 10.en_US
dc.identifier.citedreferenceSamuelson UK, Ahlmen EM. Development and evaluation of a patient education program for persons with systemic sclerosis (scleroderma). Arthritis Care Res 2000; 13: 141 – 8.en_US
dc.identifier.citedreferenceBrown SJ, Somerset ME, McCabe CS, McHugh NJ. The impact of group education on participants' management of their disease in lupus and scleroderma. Musculoskeletal Care 2004; 2: 207 – 17.en_US
dc.identifier.citedreferenceKwakkenbos L, Bluyssen SJ, Vonk MC, van Helmond AF, van den Ende CH, van den Hoogen FH, et al. Addressing patient health care demands in systemic sclerosis: pre‐post assessment of a psycho‐educational group programme. Clin Exp Rheumatol 2011; 29 Suppl: S60 – 5.en_US
dc.identifier.citedreferenceFries JF, Carey C, McShane DJ. Patient education in arthritis: randomized controlled trial of a mail‐delivered program. J Rheumatol 1997; 24: 1378 – 83.en_US
dc.identifier.citedreferenceLorig KR, Ritter PL, Laurent DD, Plant K. The internet‐based Arthritis Self‐Management Program: a one‐year randomized trial for patients with arthritis or fibromyalgia. Arthritis Rheum 2008; 59: 1009 – 17.en_US
dc.identifier.citedreferencePoole JL, Skipper B, Mendelson C. Evaluation of a mail‐delivered, print‐format self‐management program for persons with systemic sclerosis. Clin Rheumatol 2013; 32: 1393 – 8.en_US
dc.identifier.citedreferenceLorig K, Stewart A, Ritter P, Gonzalez V, Laurent D, Lynch J. Outcome measures for health education and other health care interventions. Thousand Oaks (CA): Sage Publications; 1996.en_US
dc.identifier.citedreferenceOsborne RH, Elsworth GR, Whitfield K. The Health Education Impact Questionnaire (heiQ): an outcomes and evaluation measure for patient education and self‐management interventions for people with chronic conditions. Patient Educ Couns 2007; 66: 192 – 201.en_US
dc.identifier.citedreferenceHibbard JH, Stockard J, Mahoney ER, Tusler M. Development of the Patient Activation Measure (PAM): conceptualizing and measuring activation in patients and consumers. Health Serv Res 2004; 39: 1005 – 26.en_US
dc.identifier.citedreferenceRadloff LS. The CES‐D scale: a self‐report depression scale for research in the general population. Appl Psychol Meas 1977; 1: 385 – 401.en_US
dc.identifier.citedreferenceFries JF, Spitz P, Kraines RG, Holman HR. Measurement of patient outcome in arthritis. Arthritis Rheum 1980; 23: 137 – 45.en_US
dc.identifier.citedreferenceVan der Vaart R, Repping‐Wuts H, Drossaert CH, Taal E, Knaapen‐Hans HK, van de Laar MA. Needs for online information and support of patients with systemic sclerosis. Arthritis Care Res (Hoboken) 2013; 65: 594 – 600.en_US
dc.identifier.citedreferenceBassel M, Hudson M, Taillefer SS, Schieir O, Baron M, Thombs BD. Frequency and impact of symptoms experienced by patients with systemic sclerosis: results from a Canadian national study. Rheumatology (Oxford) 2011; 50: 762 – 7.en_US
dc.identifier.citedreferenceSuarez‐Almazon ME, Kallen MA, Roundtree AK, Mayes M. Disease burden and symptom burden in systemic sclerosis: a patient perspective. J Rheumatol 2007; 34: 1718 – 26.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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