A Pilot Study of Cancer Care Companion, An Electronic Health Record Tool to Improve Information Exchange and Self-Management in Pediatric Cancer
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Tool feasibility
研究概览
简要总结
This study invites parents of children with cancer to use an electronic health record (EHR)-based communication tool, called the Cancer Care Companion, and assess the acceptability, appropriateness, and feasibility of the tool.
详细描述
High-quality communication between clinicians and parents is critical to providing optimal care for pediatric cancer. This study engages parents of children with cancer to use an electronic health record (EHR)-based communication tool, called the Cancer Care Companion, and assess the acceptability, appropriateness, and feasibility of the tool. Parent participants will be given 3 months of access to Cancer Care Companion, after which the participant(s) will complete a semi-structured interview. Participants will also complete a survey of validated measures before and after the intervention.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Eligibility Criteria for Parents:
- •Parents of children with cancer will be enrolled if they meet the following criteria:
- •They are a legal guardian of a child diagnosed with cancer in the prior 4 weeks.
- •The child plans to receive or currently receives cancer directed therapy at St. Louis Children's Hospital.
- •The parent or legal guardian has access to internet through a computer or smart phone.
- •Speaks and reads in English
- •The parent or legal guardian agrees to enroll in Epic MyChart to access a proxy portal for their child.
- •Eligibility Criteria for Clinicians:
- •Clinicians with patients who have parents participating may be enrolled. Clinician participants will be employed at SLCH or Washington University School of Medicine (WUSM). The clinicians will include physicians, nurse practitioners, and nurse coordinators from the leukemia/lymphoma, brain tumor, and solid tumor teams in order to represent the breadth of pediatric cancer diagnoses.
排除标准
- 未提供
研究组 & 干预措施
All Participants
All participants receive the Cancer Care Companion program. There is no control or comparison group.
干预措施: Cancer Care Companion (Other)
结局指标
主要结局
Tool feasibility
时间窗: Immediately post-intervention
The number of tasks marked "complete" divided by total tasks delivered, reported as a percentage per participant, with success defined as meeting or exceeding a 70% completion rate.
次要结局
- Information Exchange(Baseline and immediately post-intervention)
- Trust in Physicians(Baseline and immediately post-intervention)
- Ability to navigate the healthcare system(Baseline and immediately post-intervention)
- Caregiver burden(Baseline and immediately post-intervention)
- Parental anxiety(Baseline and immediately post-intervention)
- Communication Quality(Baseline and immediately post-intervention)
- Patient perceptions of tool usability(Immediately post-intervention)
- Patient perceptions of tool usefulness(Immediately post-intervention)
- Patient perceptions of tool barriers and facilitators(Immediately post-intervention)