I am a clinical psychologist and researcher. In my patient care, I specialize in treating adolescents and young adults with conditions such as chronic pain and sickle cell disease. I seek to help them with managing their disease, treatment adherence and transitioning to adult healthcare.
I am the co-director of Innovations in Community Research in Cincinnati Children’s Division of Behavioral Medicine and Clinical Psychology. I also direct Cincinnati Children’s Center for Clinical and Translational Science and Training (CCTST) Community Engagement Core where I help the community and researchers work together on health projects.
I was inspired to work with young people after I lost a childhood friend to cancer. I chose to do research because I wanted to help as many children and families as I could. With my research, I strive to learn the best ways for the medical team and patients and families to work together to improve treatment and the family's quality of life.
My areas of research interest include self-management, treatment adherence, healthcare transition, recruitment and retention of minorities in research, integrating design thinking into research, implementation science and community engagement.
I hope to find answers to a number of questions with my research, including:
Engaging patients and communities allows us to develop innovative and feasible solutions to health challenges.
I am proud to be an elected fellow of the American Psychological Association (APA) and to have received their Division 54 Diversity Award. I’m also a committee member for the National Academies of Sciences, Engineering, and Medicine’s effort titled Addressing Sickle Cell Disease: A Strategic Plan and Blueprint for Action.
PsyD: Wright State University, Dayton, Ohio, 1995.
Residency: Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Fellowship: Clinical Psychology, INTERACT Behavioral Healthcare Services Inc, Columbus, OH, 1995-1996.
Adolescents and young adults; sickle cell disease; transition to adult care; chronic pain; migraines; diversity and inclusion
Community-engaged research; self-management; quality improvement; sickle cell disease; health disparities; patient centered outcomes; shared decision making; health services research
Prevalence, Predictors, and Moderators of Transfer in Primary Care. Health Care Transitions. 2026; 4:100126.
Physical activity among adolescents and young adults living with chronic pain and sickle cell disease: a qualitative examination. Journal of Pediatric Psychology. 2025; 50(12):1079-1087.
Partnering With Patients and Families on the Roadmap for Emotional Health. Journal of Participatory Research Methods. 2025; 6(4).
Community Health Worker and Mobile Health Interventions for Quality of Life Among Young Adults With Sickle Cell Disease: A Randomized Clinical Trial. JAMA Network Open. 2025; 8(11):e2543571.
Disease stigma and salivary stress biomarkers among adolescents and young adults with sickle cell disease. Blood. 2025; 146(Supplement 1):2670.
Randomized controlled trial-in-progress of an interdisciplinary treatment program for youth with chronic SCD pain: Integrative strong body and mind training for sickle cell disease (I-STRONG) Blood. 2025; 146(Supplement 1):4753.
Resilience and Mental Health in Southwest Ohio During the COVID-19 Pandemic. Ohio Journal of Public Health. 2025; 7(2).
The Community Health Workers and Mobile Health for Emerging Adults Transitioning Sickle Cell Disease Care (COMETS) Trial: Protocol for a Randomized Controlled Trial. JMIR Research Protocols. 2025; 14:e69239.
Data Sharing Experience, Guidance, and Resources From the Rare Diseases Clinical Research Network (RDCRN). Clinical and Translational Science. 2025; 18(9):e70340.
Design and Refinement of CyberCellTM, a Virtual Reality Health Education Program for Adolescents and Young Adults with Sickle Cell Disease. Journal of Medical Extended Reality. 2025; 2(1):190-202.
Lori E. Crosby, PsyD, Carole Lannon, MD, MPH9/16/2025
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