Developing and Refining an Intervention to Assess and Address Health-Related Social Needs Among Families of Children With Cancer
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Unmet Health-Related Social Needs (HRSN)
研究概览
简要总结
The purpose of this study is to design Community Enhancing Resources for Childhood cAncer support (CERCA) and refine intervention procedures to target Health-related Social Needs (HRSN) in families of children with cancer. CERCA will leverage existing community resources and create partnerships that will lead to sustainable outcomes. The hypothesis is that through context-driven co-design and community-engaged research methods, the study team will develop an acceptable intervention to target unmet HRSN in families of children with cancer.
详细描述
The first goal of this study is to identify unmet health-related social needs (HRSN) faced by families undergoing pediatric cancer care and identify health system and community resources to address these unmet HRSN. The second goal of this study is to conduct a context assessment of the current processes related to HRSN screening and referrals in the pediatric oncology clinic via individual interviews and clinical workflow observations with healthcare professionals and clinical staff in the pediatric oncology clinic.
Participants of this study will include caregivers of children in cancer care, representatives of community-based organizations that provide resources for families of children with cancer, and healthcare professionals. The study involves virtual or in-person interviews and co-design workshops and will not alter the treatment decisions made by the enrolling investigator or management of the participant's health.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Caregivers of Children with Cancer
- •A caregiver of a child (<18 years old) actively receiving treatment or recently completed treatment (within the past 1 year prior to enrollment) for any type of cancer. A caregiver is defined as any individual involved in bringing the child to the clinic or providing care at home, the hospital, or other healthcare setting (e.g., parents, guardians, siblings, etc.).
- •Ability to understand IRB-approved information sheet and willingness to provide consent.
- •Age ≥ 18 years at the time of consent.
- •Ability to understand the English and/or Spanish language.
- •Community-based Organizations
- •Representative of community-based organizations that provide resources for families of children with cancer
- •Ability to understand IRB-approved information sheet and willingness to provide consent.
- •Age ≥ 18 years at the time of consent.
- •Ability to understand English and/or Spanish language.
- •Healthcare Professionals
- •Physicians, advanced practice practitioners, nurses, clinical social workers, medical assistants, clinic patient service representatives, and cancer center administrators at AHWFBC.
- •Ability to understand IRB-approved information sheet and willingness to provide consent.
- •Age ≥ 18 years at the time of consent.
- •Ability to understand English and/or Spanish language.
排除标准
- •There are no specific exclusion criteria.
研究组 & 干预措施
Caregivers, Community-Based Organizations, and Healthcare Professionals
Caregivers of children undergoing cancer care, representatives of community-based organizations that provide resources for families of children with cancer, and healthcare providers of children undergoing cancer care
干预措施: Community Enhancing Resources for Childhood cAncer support (CERCA) (Other)
结局指标
主要结局
Unmet Health-Related Social Needs (HRSN)
时间窗: Baseline
Identification of unmet health-related social needs (HRSN) faced by families undergoing pediatric cancer care and identify health system and community resources to address these unmet HRSN
Processes of HRSN screening and referrals
时间窗: Approximately 10 months after study initiation
Context assessment of the current processes related to HRSN screening and referrals in the pediatric oncology clinic via individual interviews and clinical workflow observations with healthcare professionals and clinical staff in the pediatric oncology clinic.
次要结局
- To develop CERCA (Community Enhancing Resources for Childhood cAncer support)(Approximately 15 months after study initiation)