Physical Activity Interventions for Young Cancer Survivors
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 34
- 试验地点
- 2
- 主要终点
- Physical Activity
研究概览
简要总结
The proposed mixed methods pilot study will enroll 20 young breast cancer survivors into a 12-week technology-based, remotely-delivered, peer-moderated physical activity program to examine the effects of the intervention on objectively measured physical activity and multiple aspects of quality of life; and conduct qualitative analyses to refine the intervention for a future randomized controlled trial.
详细描述
Young breast cancer survivors (i.e. those < 50 years old) have lower survival rates than their older counterparts and experience unique physical and mental challenges associated with their cancer treatments. Depression, anxiety, and poor body image are common in young breast cancer survivors. Research in older breast cancer survivors has shown that physical activity can decrease cancer recurrence and mortality, and improve many aspects of quality of life. Few physical activity intervention studies have been conducted in young breast cancer survivors, despite the fact that young survivors would be best served by age-specific interventions designed to target their needs. Remotely-delivered, technology-based interventions may be important to help young breast cancer survivors overcome unique barriers to increasing physical activity and improving quality of life.
The study aims are: 1) Explore the feasibility and acceptability of a technology-based, remotely-delivered, peer-moderated physical activity intervention for young breast cancer survivors; 2a) Assess the invention's impact on change in physical activity; and 2b) Measure the intervention's effect on multiple aspects of quality of life
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 55 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Diagnosed with breast cancer between 18-49 years old
- •Completed active treatment (chemotherapy, radiation) at least 6 months prior to enrollment
- •Self-report low levels of moderate to vigorous physical activity each week
- •Accessible by phone or video chat
- •Have a Fitbit compatible cellphone, tablet, or laptop with Internet
排除标准
- •medical condition that could make it potentially unsafe to be in an unsupervised physical activity intervention
- •currently pregnant
- •unable to commit to intervention schedule
结局指标
主要结局
Physical Activity
时间窗: Baseline to 12 weeks
The ActiGraph GT3X+ accelerometer will be used to measure change in minutes of moderate to vigorous physical activity from baseline to 12 weeks. For 7 days around each assessment time point, participants will wear the accelerometer.
次要结局
- Female Sexual Function Index(Baseline to 12 weeks)
- Body Image Scale(Baseline to 12 weeks)
- PROMIS Cancer - Fatigue(Baseline to 12 weeks)
研究者
Sheri Hartman
Assistant Professor
University of California, San Diego