Literature DB >> 11926191

Self-care in adults with sickle cell disease.

Jennifer M Lenoci1, Joseph Telfair, Heather Cecil, Robert F R Edwards.   

Abstract

This article summarizes the psychometric evaluation of the Chronic Illness Assessment Interview for Sickle Cell Disease (CIAI-SCD), an instrument based on a model of self-care for adult patients with chronic medical conditions. The CIAI-SCD was administered to 104 adults with sickle cell disease. A factor analysis identified three factors that reflected the psychological constructs of Personal Satisfaction and Perceived Control (Factor 1), Feeling Concerned and Worried (Factor 2), and Feeling Supported (Factor 3). Preliminary evidence for the internal consistency, test-retest reliability content validity, and construct validity of the CIAI-SCD was obtained. After further refinement and validation, the CIAI-SCD may be a useful tool for assessing factors related to self-care skills among adults with sickle cell disease.

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Year:  2002        PMID: 11926191     DOI: 10.1177/01939450222045879

Source DB:  PubMed          Journal:  West J Nurs Res        ISSN: 0193-9459            Impact factor:   1.967


  10 in total

1.  Successful Aging with Sickle Cell Disease: Using Qualitative Methods to Inform Theory.

Authors:  Coretta M Jenerette; Gloria Lauderdale
Journal:  J Theory Constr Test       Date:  2008-04-01

2.  Assessing Disease Knowledge and Self-Management in Youth With Sickle Cell Disease Prior to Transition.

Authors:  Barbara Speller-Brown; Maureen Varty; Lisa Thaniel; Marni B Jacobs
Journal:  J Pediatr Oncol Nurs       Date:  2018-12-19       Impact factor: 1.636

3.  Spirituality, Self-Efficacy, and Quality of Life among Adults with Sickle Cell Disease.

Authors:  Maxine Adegbola
Journal:  South Online J Nurs Res       Date:  2011-04

4.  Sleep Quality, Pain and Self-Efficacy among Community-Dwelling Adults with Sickle Cell Disease.

Authors:  Maxine Adegbola
Journal:  J Natl Black Nurses Assoc       Date:  2015-07

5.  A biopsychosocial-spiritual model of chronic pain in adults with sickle cell disease.

Authors:  Lou Ella V Taylor; Nancy A Stotts; Janice Humphreys; Marsha J Treadwell; Christine Miaskowski
Journal:  Pain Manag Nurs       Date:  2011-12-14       Impact factor: 1.929

6.  Attitudes toward clinical trials among patients with sickle cell disease.

Authors:  Carlton Haywood; Sophie Lanzkron; Marie Diener-West; Jennifer Haythornthwaite; John J Strouse; Shawn Bediako; Gladys Onojobi; Mary Catherine Beach
Journal:  Clin Trials       Date:  2014-06       Impact factor: 2.486

7.  Adult sickle cell quality-of-life measurement information system (ASCQ-Me): conceptual model based on review of the literature and formative research.

Authors:  Marsha J Treadwell; Kathryn Hassell; Roger Levine; San Keller
Journal:  Clin J Pain       Date:  2014-10       Impact factor: 3.442

8.  Self-care in Patient with Major Thalassemia: A Grounded Theory.

Authors:  Batool Pouraboli; Heidar Ali Abedi; Abbass Abbaszadeh; Majid Kazemi
Journal:  J Caring Sci       Date:  2017-06-01

9.  Exploring self-management in adult sickle cell disease patients' at a Teaching Hospital in Ghana.

Authors:  Ninon P Amertil; Elikem Keli Ayitey; Doris Grace Kpongboe; Priscilla Y A Attafuah
Journal:  Nurs Open       Date:  2020-12-27

10.  The Effectiveness of self management program on quality of life in patients with sickle cell disease.

Authors:  M Ahmadi; S Jahani; S Poormansouri; A Shariati; H Tabesh
Journal:  Iran J Ped Hematol Oncol       Date:  2015-03-15
  10 in total

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