The Adolescent and Caregiver Sickle Cell Disease Self-management Skills Checklist: Preliminary Reliability and Validity

被引:3
作者
Loew, Megan [1 ]
Williams, Justin L. [2 ]
Russell, Kathryn [1 ]
Rupff, Rebecca [1 ]
Hankins, Jane S. [3 ]
Porter, Jerlym [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Psychol, 262 Danny Thomas Pl,Mail Stop 740, Memphis, TN 38105 USA
[2] St Jude Childrens Res Hosp, Dept Hematol, 332 N Lauderdale St, Memphis, TN 38105 USA
[3] Southeast Permanente Med Grp, Atlanta, GA USA
关键词
sickle cell disease; adolescent; caregiver; disease self-management; psychometrics; TRANSITION READINESS; YOUNG-ADULTS; CARE; CONSISTENCY; CHILDREN; ALPHA; TRAQ;
D O I
10.1097/MPH.0000000000001618
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adolescents with sickle cell disease (SCD) need assistance in developing the knowledge and skills that contribute to increased disease self-management and successful transition to adult-based health care. This study evaluated the preliminary psychometric properties of the Self-Management Skills Checklist (SMSC and SMSC-C; Adolescent and Caregiver versions), a measure of perceived SCD-specific knowledge and skills. A retrospective cohort study included 114 adolescents (mean = 15.6 y) and their caregivers. We examined internal structure and reliability, score changes over time, and group differences. Cronbach coefficient alphas were 0.79 and 0.74 for caregiver-reported Skills and caregiver-reported knowledge, respectively, and 0.77 and 0.44 for adolescent-reported skills and adolescent-reported knowledge, respectively, indicating good internal consistency for 3 of the subscales. Poor reliability in the adolescent-reported knowledge summary score and factor analysis suggest an interpretation item-by-item, independent of one another. Participant group differences in age and chronic transfusion treatment existed in both summary and subscale scores of the SMSC and SMSC-C. Follow-up administrations of the scales indicated an increase in caregiver-reported skills for their adolescents from time 1 scores (M = 3.72 +/- 0.83) to time 2 scores (M = 3.99 +/- 0.63) (t(16) = 2.178, P = 0.045). Findings provide preliminary support for the usage of the SMSC and continued development to improve its psychometrics.
引用
收藏
页码:12 / 19
页数:8
相关论文
共 25 条
  • [1] Clinical Report-Supporting the Health Care Transition From Adolescence to Adulthood in the Medical Home
    Cooley W.C.
    Sagerman P.J.
    Barr M.S.
    Ciccarelli M.
    Hergenroeder A.C.
    Klitzner T.S.
    Mann M.
    Pickler L.
    Strickland B.
    Thompson B.
    Weinberg S.T.
    White P.H.
    Wilkie N.C.
    Skipper S.M.
    Brin A.
    Flinn S.K.
    [J]. PEDIATRICS, 2011, 128 (01) : 182 - +
  • [2] Identification of Risk Factors for an Unsuccessful Transition from Pediatric to Adult Sickle Cell Disease Care
    Andemariam, Biree
    Owarish-Gross, Jasmine
    Grady, James
    Boruchov, Donna
    Thrall, Roger S.
    Hagstrom, J. Nathan
    [J]. PEDIATRIC BLOOD & CANCER, 2014, 61 (04) : 697 - 701
  • [3] Asnani MR, 2017, GLOB PEDIAT HLTH, V4
  • [4] Barton-Gooden A, 2018, PSYCHOL HEALTH MED, V24, P1
  • [5] The number of people with sickle-cell disease in the United States: National and state estimates
    Brousseau, David C.
    Panepinto, Julie A.
    Nimmer, Mark
    Hoffmann, Raymond G.
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2010, 85 (01) : 77 - 78
  • [6] Factors that influence adolescent adaptation to sickle cell disease
    Burlew, K
    Telfair, J
    Colangelo, L
    Wright, EC
    [J]. JOURNAL OF PEDIATRIC PSYCHOLOGY, 2000, 25 (05) : 287 - 299
  • [7] From alpha to omega: A practical solution to the pervasive problem of internal consistency estimation
    Dunn, Thomas J.
    Baguley, Thom
    Brunsden, Vivienne
    [J]. BRITISH JOURNAL OF PSYCHOLOGY, 2014, 105 (03) : 399 - 412
  • [8] A Clinical Tool to Measure the Components of Health-Care Transition from Pediatric Care to Adult Care: The UNC TRxANSITION Scale
    Ferris, Maria E.
    Harward, Donna H.
    Bickford, Kristi
    Layton, J. Bradley
    Ferris, M. Ted
    Hogan, Susan L.
    Gipson, Debbie S.
    McCoy, Lynn P.
    Hooper, Stephen R.
    [J]. RENAL FAILURE, 2012, 34 (06) : 744 - 753
  • [9] Neurocognitive Deficits in Children With Sickle Cell Disease: A Comprehensive Profile
    Hijmans, Channa T.
    Fijnvandraat, Karin
    Grootenhuis, Martha A.
    van Geloven, Nan
    Heijboer, Harriet
    Peters, Marjolein
    Oosterlaan, Jaap
    [J]. PEDIATRIC BLOOD & CANCER, 2011, 56 (05) : 783 - 788
  • [10] Development of a screening instrument of adherence in pediatric sickle cell disease
    Hilker, Kellie A.
    Jordan, Sara Sytsma
    Jensen, Scott
    Elkin, T. David
    Iyer, Rathi
    [J]. CHILDRENS HEALTH CARE, 2006, 35 (03) : 235 - 246