NCT05150028已完成不适用
A Virtual Intervention to Improve Medication Adherence in Pediatric Cancer: MedSupport
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 17
- 试验地点
- 2
- 主要终点
- Retention rates
研究概览
简要总结
To develop a cancer center level practice intervention to promote treatment adherence and reduce outcome disparities in pediatric cancer survivors
详细描述
To conduct a pilot study to assess the feasibility and acceptability of the Social Determinants of Adherence intervention
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 1 Year 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Parents/caregivers of pediatric patients must meet the following criteria to be eligible:
- •Parents/guardians of child that has been diagnosed with any cancer.
- •Parents/guardians of child with any cancer between age 0 and
- •Parents/guardians of child on home-based oral anti-cancer therapy or supportive care therapy.
- •The clinician for the family agrees to participate in the study.
排除标准
- •Participants will be excluded from this study if unwilling or unable to complete the assessment in English
结局指标
主要结局
Retention rates
时间窗: Up to 8 weeks
Feasibility of intervention as assessed by retention rates
次要结局
- Feasibility of universal SDOA screening(up to 8 weeks)
- Provider satisfaction with barrier reports(up to 8 weeks)
研究者
研究点 (2)
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