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临床试验/NCT05048316
NCT05048316已完成不适用

Pilot Study to Develop a Group-Based E-Health Intervention for Young Adult Cancer Survivors

H. Lee Moffitt Cancer Center and Research Institute1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2021年5月11日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
17
试验地点
1
主要终点
Session attendance after the intervention - Acceptability

研究概览

简要总结

Investigators will test an evidence-based behavioral intervention that is responsive to Young Adults (YA's) expressed needs and priorities

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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
是

入选标准

  • •18-39 years old
  • •Diagnosed with cancer between 18-39 years old
  • •Cancer diagnosis was non-metastatic
  • •Completed cancer treatment between 1 month and 5 years prior to enrollment, with the exception of ongoing hormone therapy
  • •No documented or observable psychiatric or neurological disorders that could interfere with participation (e.g., active psychosis, active substance abuse), as identified by the referring medical team, chart review, or screening
  • •Able to speak and read English
  • •Able to provide informed consent

排除标准

  • •Metastatic disease
  • •Continued cancer treatment
  • •Psychiatric or neurological disorders that could interfere with study participation
  • •Vulnerable populations will not be included

研究组 & 干预措施

eHealth

Experimental

Weekly video conference groups led by a trained facilitator

干预措施: Cognitive-Behavioral Stress Management and Health Education (Behavioral)

结局指标

主要结局

Session attendance after the intervention - Acceptability

时间窗: Immediately after the intervention

Videoconference delivery will be acceptable if average group attendance is ≥6/10 sessions.

Satisfaction assessed by study-specific survey during the intervention - Acceptability

时间窗: During intervention

The intervention will be deemed acceptable if, on average, participants report satisfaction with the weekly sessions as ≥2 on a 0-4 scale.

Satisfaction assessed by study-specific survey after the intervention - Acceptability

时间窗: Immediately after the intervention

The intervention will be deemed acceptable if, on average, participants report satisfaction with the overall program and intent to continue using the intervention skills as ≥2 on a 0-4 scale.

次要结局

  • Quality of life before intervention(Baseline)
  • Change in quality of life at after intervention(Immediately after intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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