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Family Functioning and Medical Adherence Across Children and Adolescents With Chronic Health Conditions: A Meta-Analysis

Journal of pediatric psychology, 2019-01, Vol.44 (1), p.84-97

2019

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Quality of life of caregivers at the end of their child's pediatric cancer treatment: cancer-specific worry and material hardship

Journal of pediatric psychology, 2024-05, Vol.49 (5), p.348-355

2024

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Caregiver condition management and family functioning after pediatric cancer treatment: Moderation by race and ethnicity

Psycho-oncology (Chichester, England), 2024-01, Vol.33 (1), p.e6263-n/a

2024

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Screening for Family Psychosocial Risk in Pediatric Cancer: Validation of the Psychosocial Assessment Tool (PAT) Version 3

Journal of pediatric psychology, 2018-08, Vol.43 (7), p.737-748

2018

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Health-Related Quality of Life at Diagnosis for Pediatric Thyroid Cancer Patients

The journal of clinical endocrinology and metabolism, 2023-05, Vol.108 (5), p.e169-e177

2023

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An Updated Equitable Model of Readiness for Transition to Adult Care: Content Validation in Young People With Sickle Cell Disease

JAMA pediatrics, 2024-03

2024

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Caregiver distress and patient health‐related quality of life: psychosocial screening during pediatric cancer treatment

Psycho-oncology (Chichester, England), 2017-10, Vol.26 (10), p.1555-1561

2017

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Reply to Assessing clinical trial effects on outcomes among pediatric and adolescent and young adult (AYA) patients with cancer

Cancer, 2021-02, Vol.127 (4), p.649-650

2021

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Cancer-Related Decision-Making Among Adolescents, Young Adults, Caregivers, and Oncology Providers

Qualitative health research, 2021-11, Vol.31 (13), p.2355-2363

2021

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Longitudinal predictors of caregiver resilience outcomes at the end of childhood cancer treatment

Psycho-oncology (Chichester, England), 2021-05, Vol.30 (5), p.747-755

2021

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Pediatric Psychosocial Preventative Health Model: Achieving Equitable Psychosocial Care for Children and Families

Families systems & health, 2024-03, Vol.42 (1), p.76-89

2024

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Assessing the psychosocial needs and program preferences of adolescents and young adults with cancer

Supportive care in cancer, 2016-02, Vol.24 (2), p.823-832

2016

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Friendships in Pediatric Brain Tumor Survivors and Non-Central Nervous System Tumor Survivors

Journal of pediatric psychology, 2020-03, Vol.45 (2), p.194-202

2020

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Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress

Health and quality of life outcomes, 2008-08, Vol.6 (1), p.60-60

2008

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Mistrust of Pediatric Sickle Cell Disease Clinical Trials Research

American journal of preventive medicine, 2016-07, Vol.51 (1), p.S78-S86

2016

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Acceptability and Feasibility in a Pilot Randomized Clinical Trial of Computerized Working Memory Training and Parental Problem-Solving Training With Pediatric Brain Tumor Survivors

Journal of pediatric psychology, 2019-07, Vol.44 (6), p.669-678

2019

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Providing Children and Adolescents Opportunities for Social Interaction as a Standard of Care in Pediatric Oncology

Pediatric blood & cancer, 2015-12, Vol.62 (S5), p.S674-S699

2015

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The pervasive influence of systems of power on transition readiness for adult care in sickle cell disease: A qualitative study

Pediatric blood & cancer, 2024-09, Vol.71 (9), p.e31156

2024

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Screening for psychosocial risk in pediatric cancer

Pediatric blood & cancer, 2012-11, Vol.59 (5), p.822-827

2012

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Quality of life of adolescents with cancer: family risks and resources

Health and quality of life outcomes, 2010-06, Vol.8 (1), p.63-63

2010

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Provider Perspectives on the Implementation of Psychosocial Risk Screening in Pediatric Cancer

Journal of pediatric psychology, 2017-07, Vol.42 (6), p.700-710

2017

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Advancing health equity in pediatric cancer through implementation of universal family psychosocial risk screening

Psycho-oncology (Chichester, England), 2022-09, Vol.31 (9), p.1483-1490

2022

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Psychosocial needs of pediatric cancer patients and their caregivers at end of treatment: Why psychosocial screening remains important

Pediatric blood & cancer, 2023-09, Vol.70 (9), p.e30540-n/a

2023

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Measures of Readiness to Transition to Adult Health Care for Youth With Chronic Physical Health Conditions: A Systematic Review and Recommendations for Measurement Testing and Development

Journal of pediatric psychology, 2014-07, Vol.39 (6), p.588-601

2014

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Implementation of family psychosocial risk assessment in pediatric cancer with the Psychosocial Assessment Tool (PAT): study protocol for a cluster-randomized comparative effectiveness trial

Implementation science : IS, 2020-07, Vol.15 (1), p.1-60, Article 60

2020

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Family Functioning and Medical Adherence Across Children and Adolescents With Chronic Health Conditions: A Meta-Analysis

Quality of life of caregivers at the end of their child's pediatric cancer treatment: cancer-specific worry and material hardship

Caregiver condition management and family functioning after pediatric cancer treatment: Moderation by race and ethnicity

Screening for Family Psychosocial Risk in Pediatric Cancer: Validation of the Psychosocial Assessment Tool (PAT) Version 3

Health-Related Quality of Life at Diagnosis for Pediatric Thyroid Cancer Patients

An Updated Equitable Model of Readiness for Transition to Adult Care: Content Validation in Young People With Sickle Cell Disease

Caregiver distress and patient health‐related quality of life: psychosocial screening during pediatric cancer treatment

Reply to Assessing clinical trial effects on outcomes among pediatric and adolescent and young adult (AYA) patients with cancer

Cancer-Related Decision-Making Among Adolescents, Young Adults, Caregivers, and Oncology Providers

Longitudinal predictors of caregiver resilience outcomes at the end of childhood cancer treatment

Pediatric Psychosocial Preventative Health Model: Achieving Equitable Psychosocial Care for Children and Families

Assessing the psychosocial needs and program preferences of adolescents and young adults with cancer

Friendships in Pediatric Brain Tumor Survivors and Non-Central Nervous System Tumor Survivors

Quality of life among adolescents with sickle cell disease: mediation of pain by internalizing symptoms and parenting stress

Mistrust of Pediatric Sickle Cell Disease Clinical Trials Research

Acceptability and Feasibility in a Pilot Randomized Clinical Trial of Computerized Working Memory Training and Parental Problem-Solving Training With Pediatric Brain Tumor Survivors

Providing Children and Adolescents Opportunities for Social Interaction as a Standard of Care in Pediatric Oncology

The pervasive influence of systems of power on transition readiness for adult care in sickle cell disease: A qualitative study

Screening for psychosocial risk in pediatric cancer

Quality of life of adolescents with cancer: family risks and resources

Provider Perspectives on the Implementation of Psychosocial Risk Screening in Pediatric Cancer

Advancing health equity in pediatric cancer through implementation of universal family psychosocial risk screening

Psychosocial needs of pediatric cancer patients and their caregivers at end of treatment: Why psychosocial screening remains important

Measures of Readiness to Transition to Adult Health Care for Youth With Chronic Physical Health Conditions: A Systematic Review and Recommendations for Measurement Testing and Development

Implementation of family psychosocial risk assessment in pediatric cancer with the Psychosocial Assessment Tool (PAT): study protocol for a cluster-randomized comparative effectiveness trial

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