Developing and Pre-Testing an eHealth Group Intervention for Young Adult Cancer Survivors
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 6
- 试验地点
- 2
- 主要终点
- Acceptability of the adapted intervention
研究概览
简要总结
The purpose of this study is to develop and pre-test an eHealth group intervention for young adult cancer survivors.
详细描述
In the first part of this study, the investigators adapted an evidence-based intervention for improving HRQOL to better meet the needs of young adult cancer survivors, and then conducted focus groups with young adult cancer survivors to get feedback on the adapted intervention. In the second part of the study, the investigators will conduct a single-arm pilot trial in which the adapted intervention will be delivered over videoconference via weekly group meetings with a trained facilitator over the course of 10 weeks.
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 39 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •age 18-39 years at the time of participation
- •diagnosed with a non-metastatic primary cancer between 18-39 years old
- •completed primary cancer treatment (excepting hormone therapy) 1 month to 5 years prior to enrollment
- •able to speak and read English
- •access to internet or cellular connectivity with sufficient bandwidth to participate in videoconferences
排除标准
- •metastatic disease
- •psychiatric or neurological disorders that could interfere with study participation
- •considered part of a vulnerable population
结局指标
主要结局
Acceptability of the adapted intervention
时间窗: Immediately after the intervention
Immediately after the intervention participants will report their satisfaction with the full program through a brief survey.
次要结局
- Change in coping from baseline to immediately after the intervention(Baseline and immediately after the intervention)
- Change in cancer-related distress from baseline to immediately after the intervention(Baseline and immediately after the intervention)
- Change in stress management skills self-efficacy from baseline to immediately after the intervention(Baseline and immediately after the intervention)
- Change in symptom burden from baseline to immediately after the intervention(Baseline and immediately after the intervention)
- Change in health-related quality of life (HRQOL) from baseline to immediately after the intervention(Baseline and immediately after the intervention)
研究者
Rina Fox
Research Assistant Professor
Northwestern University