HABIT Efficacy Trial Intervention Improves Elements of General and Disease‐Specific Quality of Life in Youth With Sickle Cell Disease
Fuente:
Wiley Open Access
Enregistré dans:
| Auteurs principaux: | Arlene Smaldone, Deepa Manwani, Banu Aygun, Abena Appiah‐Kubi, Kim Smith‐Whitley, Nancy S. Green |
|---|---|
| Format: | Artículo Open Access |
| Publié: |
Wiley
2025
|
| Sujets: | |
| Accès en ligne: | |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
Assessing multilevel barriers to hydroxyurea adherence in youth with sickle cell disease using pharmacy‐based refill records
par: Arlene Smaldone, et autres
Publié: (2024)
par: Arlene Smaldone, et autres
Publié: (2024)
Comment on: “Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment (HABIT) efficacy trial: Community health worker support may increase hydroxyurea adherence of youth with sickle cell disease”: Participant evaluation
par: Mary F. Martin, et autres
Publié: (2024)
par: Mary F. Martin, et autres
Publié: (2024)
Characterizing Engagement With a Mobile Health Application Designed for Adolescents and Young Adults With Sickle Cell Disease: Findings From the COMETS Study
par: Caren Steinway, et autres
Publié: (2026)
par: Caren Steinway, et autres
Publié: (2026)
The Role of Associated Treatment Factors and Mental Health on Transition From Pediatric to Adult Care for Adolescent/Young Adults With Sickle Cell Disease
par: Caryn R. R. Rodgers, et autres
Publié: (2025)
par: Caryn R. R. Rodgers, et autres
Publié: (2025)
Sickle Cell Disease‐Related Stigma: Quantitative Assessment From India
par: Bontha V. Babu, et autres
Publié: (2025)
par: Bontha V. Babu, et autres
Publié: (2025)
Unheard and Under‐Supported: Health‐Related Quality of Life in Children, Adolescents, and Young Adults With Sickle Cell Disease
par: Desiré Fantasia, et autres
Publié: (2026)
par: Desiré Fantasia, et autres
Publié: (2026)
Prevalence and Impact of Autism Spectrum Disorder and Selected Neurodevelopmental Diagnoses in Hospitalized Youth With Sickle Cell Disease
par: Megan M. Griffith, et autres
Publié: (2025)
par: Megan M. Griffith, et autres
Publié: (2025)
Caregiver Well‐Being and Pediatric Healthcare Utilization in Youth With Sickle Cell Disease: The Role of Caregiver and Child Factors
par: Theresa L. Kapke, et autres
Publié: (2025)
par: Theresa L. Kapke, et autres
Publié: (2025)
Sensitivity and Specificity of a Signaling Question for Surveillance of Cognitive Functioning in Pediatric Sickle Cell Disease
par: Steven J. Hardy, et autres
Publié: (2025)
par: Steven J. Hardy, et autres
Publié: (2025)
Sickle Cell Disease and Hemoglobin S Prevalence in Botswana
par: Setho Ruth Taboka Kgakatsi, et autres
Publié: (2025)
par: Setho Ruth Taboka Kgakatsi, et autres
Publié: (2025)
User Perceptions of a Multilevel mHealth Intervention to Boost Adherence to Hydroxyurea in Sickle Cell Disease
par: Christina M. Abrams, et autres
Publié: (2025)
par: Christina M. Abrams, et autres
Publié: (2025)
Pregnancy‐ and Disease‐Related Morbidity Among Medicaid Enrollees With Sickle Cell Disease
par: Mariam Kayle, et autres
Publié: (2025)
par: Mariam Kayle, et autres
Publié: (2025)
Association of Food Insecurity With Disease‐Related Complications and Healthcare Utilization for Patients With Sickle Cell Disease
par: Sharjeel Syed, et autres
Publié: (2025)
par: Sharjeel Syed, et autres
Publié: (2025)
Reproductive Health and Pregnancy Outcomes Among Women With Sickle Cell Disease in Tribal Communities of India: A Community‐Based Retrospective Comparative Study
par: Yogita Sharma, et autres
Publié: (2026)
par: Yogita Sharma, et autres
Publié: (2026)
Engaging Parents of Children With Sickle Cell Disease in Shared Decision‐Making for Hydroxyurea: The ENGAGE‐HU Study
par: Aimee K. Hildenbrand, et autres
Publié: (2025)
par: Aimee K. Hildenbrand, et autres
Publié: (2025)
Prevalence and Significance of Pancreatic Iron in Transfusion‐Dependent Sickle Cell Disease
par: Akhila Vadivelan, et autres
Publié: (2025)
par: Akhila Vadivelan, et autres
Publié: (2025)
Medication Utilization Among Children With Sickle Cell Disease in the United States
par: Abiodun John Ologunowa, et autres
Publié: (2025)
par: Abiodun John Ologunowa, et autres
Publié: (2025)
The Voxelotor Effect: Decreased Affinity for New Drugs for Sickle Cell Disease?
par: Charles T. Quinn, et autres
Publié: (2024)
par: Charles T. Quinn, et autres
Publié: (2024)
Hydroxyurea Therapy and Sleep‐Disordered Breathing in Children With Sickle Cell Disease
par: Zachary Abramson, et autres
Publié: (2025)
par: Zachary Abramson, et autres
Publié: (2025)
Statewide Academic Performance of High School Students With Sickle Cell Disease
par: Andrew M. Heitzer, et autres
Publié: (2025)
par: Andrew M. Heitzer, et autres
Publié: (2025)
Screening and Impact of Neuropathic Pain in Young Individuals With Sickle Cell Disease
par: Amira Adly, et autres
Publié: (2024)
par: Amira Adly, et autres
Publié: (2024)
Hospitalization Through Families’ Eyes: Comparing Inpatient Care Quality for Children With Sickle Cell Disease and Cystic Fibrosis in Canada
par: Hailey M. Zwicker, et autres
Publié: (2026)
par: Hailey M. Zwicker, et autres
Publié: (2026)
Sickle Cell Disease Is an Inherent Risk for Asthma in a Sibling Comparison Study
par: Suhei C. Zuleta De Bernardis, et autres
Publié: (2026)
par: Suhei C. Zuleta De Bernardis, et autres
Publié: (2026)
Behavioral and Electrophysiological Assessment of Central Auditory Processing in Individuals With Sickle Cell Disease
par: Rhayane Vitória Lopes, et autres
Publié: (2025)
par: Rhayane Vitória Lopes, et autres
Publié: (2025)
How We Approach Contraception for Adolescents and Young Adults With Sickle Cell Disease
par: Maayan Leroy‐Melamed, et autres
Publié: (2025)
par: Maayan Leroy‐Melamed, et autres
Publié: (2025)
Impact of Neighborhood Disadvantage on Preventive and Acute Care Utilization in Sickle Cell Disease
par: Ashley Catanzarite, et autres
Publié: (2024)
par: Ashley Catanzarite, et autres
Publié: (2024)
Systemic Inflammatory Diseases in Children With Sickle Cell Disease: A French Multicenter Observational Study on Diagnostic and Therapeutic Issues
par: Caroline Vinit, et autres
Publié: (2025)
par: Caroline Vinit, et autres
Publié: (2025)
Prevalence of Duffy Null and Its Impact on Hydroxyurea Dosing in Children With Sickle Cell Disease
par: Jill S. Menell, et autres
Publié: (2025)
par: Jill S. Menell, et autres
Publié: (2025)
Clinical Practice Patterns for Discussing Hydroxyurea Initiation With Families of Children With Sickle Cell Disease
par: Aimee K. Hildenbrand, et autres
Publié: (2026)
par: Aimee K. Hildenbrand, et autres
Publié: (2026)
Comparing Absolute Neutrophil Counts of Children With Sickle Cell Disease With and Without the Duffy Null Phenotype
par: Nate Goldfarb, et autres
Publié: (2025)
par: Nate Goldfarb, et autres
Publié: (2025)
Optimizing Transcranial Doppler Screening for Stroke Prevention in Young African Children With Sickle Cell Disease
par: Derby Tembo, et autres
Publié: (2025)
par: Derby Tembo, et autres
Publié: (2025)
Does Hydroxyurea Reduce Hospital Admissions in Patients With Both Sickle Cell Disease and Dengue Fever?
par: Narcisse Elenga, et autres
Publié: (2026)
par: Narcisse Elenga, et autres
Publié: (2026)
Osteopathic Manipulative Treatment: A Safe and Feasible Adjunct in Sickle Cell Disease Pain Management
par: Amber Brown, et autres
Publié: (2024)
par: Amber Brown, et autres
Publié: (2024)
Improving Completion Rates of Transcranial Doppler Ultrasounds in Children With Sickle Cell Disease Using Quality Improvement Efforts: In‐Clinic Versus Population‐Based Assessments
par: Madhav Vissa, et autres
Publié: (2025)
par: Madhav Vissa, et autres
Publié: (2025)
Clinical Features and Outcomes of Pneumococcal Bacteremia in Children With Sickle Cell Disease in the Pneumococcal Conjugate Vaccine Era
par: Marianne E. Yee, et autres
Publié: (2025)
par: Marianne E. Yee, et autres
Publié: (2025)
Socioeconomic Status and Stroke Risk in Pediatric Sickle Cell Disease: A DISPLACE Study Secondary Analysis
par: Jeffrey G. Edwards, et autres
Publié: (2025)
par: Jeffrey G. Edwards, et autres
Publié: (2025)
Pulmonary Dysfunction Is Associated With Sleep Study Abnormalities in Children With Sickle Cell Disease: A Multicenter Study
par: Ammar Saadoon Alishlash, et autres
Publié: (2026)
par: Ammar Saadoon Alishlash, et autres
Publié: (2026)
Delayed Presentation of Transfusion‐Associated Circulatory Overload Associated With Splenic Sequestration Management in Sickle Cell Disease
par: Laura S. Duarte, et autres
Publié: (2024)
par: Laura S. Duarte, et autres
Publié: (2024)
Correction to “Engaging Parents of Children With Sickle Cell Disease in Shared Decision‐Making for Hydroxyurea: The ENGAGE‐HU Study”
Publié: (2026)
Publié: (2026)
Treatment Experience Using a Micro‐Induction Buprenorphine Protocol for Chronic Pain in Pediatric Sickle Cell Disease
par: Ashwin Patel, et autres
Publié: (2025)
par: Ashwin Patel, et autres
Publié: (2025)
Documents similaires
-
Assessing multilevel barriers to hydroxyurea adherence in youth with sickle cell disease using pharmacy‐based refill records
par: Arlene Smaldone, et autres
Publié: (2024) -
Comment on: “Hydroxyurea Adherence for Personal Best in Sickle Cell Treatment (HABIT) efficacy trial: Community health worker support may increase hydroxyurea adherence of youth with sickle cell disease”: Participant evaluation
par: Mary F. Martin, et autres
Publié: (2024) -
Characterizing Engagement With a Mobile Health Application Designed for Adolescents and Young Adults With Sickle Cell Disease: Findings From the COMETS Study
par: Caren Steinway, et autres
Publié: (2026) -
The Role of Associated Treatment Factors and Mental Health on Transition From Pediatric to Adult Care for Adolescent/Young Adults With Sickle Cell Disease
par: Caryn R. R. Rodgers, et autres
Publié: (2025) -
Sickle Cell Disease‐Related Stigma: Quantitative Assessment From India
par: Bontha V. Babu, et autres
Publié: (2025)