Lori E Crosby

Biographic Data

ID199766
NAMELori E Crosby
GIVEN NAMESLori E
FAMILY NAMECrosby
SIGNATURECROSBY L E
AFFILIATIONSCincinnati Children's Hospital Medical Center
ORCID0000-0001-6656-7745
VERIFIEDYes
TOTAL WORKS8
TOTAL CITATIONS12
WORKS AS AUTHOR8
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2013
LATEST PUBLICATION YEAR2024
H-INDEX2

  • Pain-Related Injustice Appraisals, Sickle Cell Stigma, and Racialized Discrimination in the Youth with Sickle Cell Disease

    Open AccessMegan M Miller, Ama Kissi et al.ARTICLEJournal of Racial and Ethnic…2024References: 56

  • Evaluation of a Community Covid-19 Vaccine Ambassador Train-the-Trainer Program

    Open AccessAlexandra M S Corley, Stacey M Gomes et al.ARTICLEJournal of Immigrant and Minority…2023

    Racially minoritized groups are more likely to experience COVID-19 vaccine hesitancy and have lower vaccination rates. As part of a multi-phase community-engaged project, we developed a train-the-trainer program in response to a needs assessment. "Community vaccine ambassadors" were trained to address COVID-19 vaccine hesitancy. We evaluated the program's feasibility, acceptability, and impact on participant confidence for COVID-19 vaccination co…

  • Psychologists as leaders in equitable science

    Open AccessDesireé N Williford, Emily McTate et al.ARTICLEAmerican Psychologist2023References: 7

    Psychologists have an ethical responsibility to advance health equity and can play a significant role in improving health care experiences for families racialized as Black, including those with sickle cell disease (SCD), a group of genetic blood disorders primarily affecting communities of color. Parents of children with SCD report experiences of stigma and discrimination due to racism in the health care system. The current commentary describes t…

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

    Anna Hood, Lori E Crosby et al.ARTICLEEthnicity and Health2020Cited by: 6References: 5

    Objectives: Individuals with sickle cell disease (SCD) experience significant health problems that may result in unpredictable pain episodes and frequent healthcare utilization. Disparities in clinical care may contribute to health-related stigma and racial bias for this majority African-American/Black population. There is less known about the influence of health-related stigma and racial bias on the health-related quality of life (HRQOL) of chil…

  • Halo or horn? A qualitative study of mothers’ experiences with feeding children during the first year following bariatric surgery

    Open AccessMeg H Zeller, Shannon M Robson et al.ARTICLEAppetite2019References: 45

  • Translating sickle cell guidelines into practice for primary care providers with Project Echo

    Open AccessLisa M Shook, Christina Bennett Farrell et al.ARTICLEMedical Education Online2016

    STORM TeleECHO has the potential to increase implementation of the NHLBI evidence-based guidelines, especially increased use of hydroxyurea, resulting in improvements in the quality of care and outcomes for children and young adults with SCD. This model could be replicated in other pediatric chronic illness conditions to improve PCP knowledge and confidence in delivering evidence-based care

  • Eating dinner away from home

    Open AccessShannon M Robson, Lori E Crosby et al.ARTICLEAppetite2016Cited by: 6References: 29

  • Understanding the Experiences of Youth Living With Sickle Cell Disease

    Jessica M Valenzuela, Lisa M Vaughn et al.ARTICLEFamily & Community Health2013

    A Photovoice pilot was conducted with youth living with sickle cell disease (SCD), in order to further understand their lived experience and examine the acceptability, feasibility, and utility of this method in this population. SCD is an inherited genetic condition whose primary symptom is severe pain. Youth were able to reflect on their experiences with SCD using Photovoice and the adapted SHOWeD method. Parents and youth found Photovoice to be …