跳至主要内容
临床试验/NCT06651190
NCT06651190尚未招募不适用

Building mHealth Parent Capacity to Manage Pain in Young Children With Cancer: A Pilot Randomized Controlled Trial

The Hospital for Sick Children2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
40
试验地点
2
主要终点
Feasibility - attrition

研究概览

简要总结

Pain is a problem for children with cancer, especially when they are outside of the hospital setting. Younger children with cancer are particularly vulnerable to undermanaged pain because of their inability to self-report pain and their reliance on parents for treatment. One method to help these children to get the best care possible is through the use of smartphone-based mHealth solutions. Smartphone apps can provide treatment advice to patients experiencing pain in real-time and in any environment. This research will use a phased and user-centered approach with family caregivers to co-design and co-evaluate the new cancer Pain Caregiver Resource (PainCaRe) app to achieve the following aims: (1) high-fidelity software development and usability refinement; (2) evaluation of trial feasibility and preliminary effectiveness in a pilot randomized controlled trial (RCT); and (3) systematic analysis of caregiver app usage patterns to refine PainCaRe for optimal engagement prior to a future RCT.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Device Feasibility
盲法
Single (Investigator)

入排标准

性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Feasibility - attrition

时间窗: 1 year

Percent of caregivers not completing 8-week outcome measures. Criteria for feasibility: attrition \<25%.

Feasibility - accrual

时间窗: 1 year

Percent of eligible caregivers accrued per recruitment day. Criteria for feasibility: accrual \>60%.

Feasibility - adherence

时间窗: 8 weeks

Adherence to the intervention will be measured using the Analytics Platform to Evaluate Effective Engagement (APEEE) platform, a proprietary analytics software measuring the number of once-daily pain assessments completed and engagement with pain treatment guidance. Criteria for feasibility: adherence to twice-daily pain reporting \>65%.

Acceptability

时间窗: 8 weeks

Measured with the Acceptability E-Scale (AES). Criteria for acceptability: mean score of 4 on each item

次要结局

  • Child pain intensity - parent report(8 weeks)
  • Child pain intensity - child report(8 weeks)
  • Child pain interference - parent report(8 weeks)
  • Child pain interference - child report(8 weeks)
  • Child health-related quality of life - parent report(8 weeks)
  • Child health-related quality of life - child report(8 weeks)
  • Parent quality of life(8 weeks)
  • Parent pain management self-efficacy(8 weeks)
  • Parent care satisfaction(8 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Lindsay Jibb

Principal Investigator

The Hospital for Sick Children

研究点 (2)

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