Literature DB >> 22646200

Preliminary validity and reliability of the Sickle Cell Disease Health-Related Stigma Scale.

Coretta Jenerette1, Cheryl A Brewer, Jamie Crandell, Kenneth I Ataga.   

Abstract

There have been no published studies that measure health-related stigma in individuals with sickle cell disease (SCD). This study provides preliminary validity and reliability of the Sickle Cell Disease Health-Related Stigma Scale (SCD-HRSS). Using a sample of 77 young adults with SCD, ages 18-35 years, the results support the reliability of the SCD-HRSS with an overall Cronbach's alpha reliability of 0.84 and construct validity with a positive correlation between SCD-HRSS and a measure of depressive symptoms. Participants reported the highest levels of perceived stigma from the general public, then doctors, and lastly family. Limitations and directions for future research are discussed.

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Year:  2012        PMID: 22646200     DOI: 10.3109/01612840.2012.656823

Source DB:  PubMed          Journal:  Issues Ment Health Nurs        ISSN: 0161-2840            Impact factor:   1.835


  10 in total

1.  Stigma of Sickle Cell Disease: A Systematic Review.

Authors:  Dominique Bulgin; Paula Tanabe; Coretta Jenerette
Journal:  Issues Ment Health Nurs       Date:  2018-04-13       Impact factor: 1.835

2.  Depressive symptoms and sickle cell pain: The moderating role of internalized stigma.

Authors:  Breanna M Holloway; Lakeya S McGill; Shawn M Bediako
Journal:  Stigma Health       Date:  2017-11

3.  Nurses' attitudes toward patients with sickle cell disease: a worksite comparison.

Authors:  Coretta M Jenerette; Bosny J Pierre-Louis; Nadine Matthie; Yasmeen Girardeau
Journal:  Pain Manag Nurs       Date:  2015-06       Impact factor: 1.929

4.  The Measure of Sickle Cell Stigma: Initial findings from the Improving Patient Outcomes through Respect and Trust study.

Authors:  Shawn M Bediako; Sophie Lanzkron; Marie Diener-West; Gladys Onojobi; Mary C Beach; Carlton Haywood
Journal:  J Health Psychol       Date:  2014-07-04

5.  Care seeking for pain in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl A Brewer; Kenneth I Ataga
Journal:  Pain Manag Nurs       Date:  2013-01-21       Impact factor: 1.929

Review 6.  Systematic literature review and assessment of patient-reported outcome instruments in sickle cell disease.

Authors:  Grammati Sarri; Menaka Bhor; Seye Abogunrin; Caroline Farmer; Savita Nandal; Rashid Halloway; Dennis A Revicki
Journal:  Health Qual Life Outcomes       Date:  2018-05-21       Impact factor: 3.186

7.  Conceptualizing pain-related stigma in adolescent chronic pain: a literature review and preliminary focus group findings.

Authors:  Emily O Wakefield; William T Zempsky; Rebecca M Puhl; Mark D Litt
Journal:  Pain Rep       Date:  2018-09-11

8.  Psychosocial and Clinical Risk Factors Associated with Substance Use in Observational Cohort of Patients with Sickle Cell Disease.

Authors:  J Deanna Wilson; Sophie Lanzkron; Lydia H Pecker; Shawn M Bediako; Dingfen Han; Mary Catherine Beach
Journal:  Subst Use Misuse       Date:  2020-08-07       Impact factor: 2.164

9.  The influence of perceived racial bias and health-related stigma on quality of life among children with sickle cell disease.

Authors:  Anna M Hood; Lori E Crosby; Eva Hanson; Lisa M Shook; Jeffrey D Lebensburger; Avi Madan-Swain; Megan M Miller; Zina Trost
Journal:  Ethn Health       Date:  2020-09-08       Impact factor: 2.732

10.  Not being heard: barriers to high quality unplanned hospital care during young people's transition to adult services - evidence from 'this sickle cell life' research.

Authors:  Alicia Renedo; Sam Miles; Subarna Chakravorty; Andrea Leigh; Paul Telfer; John O Warner; Cicely Marston
Journal:  BMC Health Serv Res       Date:  2019-11-21       Impact factor: 2.655

  10 in total

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