Improving Physical Activity in Rural Cancer Survivors
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Mayo Clinic
- 入组人数
- 100
- 试验地点
- 4
- 主要终点
- Rate of adherence to program based on participation in virtual exercise sessions
研究概览
简要总结
The purpose of this study is to determine if increasing physical activity (PA) will increase physical functioning, as measured by cardiovascular endurance, muscular strength, and balance in underserved adult cancer survivors > 60 years of age and/or those of any age residing at a rural address. Also, to determine if increasing PA will increase quality of life (QOL), as measured by physical functioning and fatigue, in underserved cancer survivors >60 years of age and/or those of any age residing at a rural address.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Adult, cancer survivors (no active disease) at Mayo Clinic Health System (MCHS) in Northwest Wisconsin (NWWI), Southwest Wisconsin (SWWI), Southeast Minnesota (SEMN), or Southwest Minnesota (SWMN)
- •Any stage cancer
- •Age >= 18 years residing at a rural address (as defined by Rural America, census.gov Urban Areas 2020 metric)
- •Age ≥ 18 years residing at a rural address (as defined by Rural America, census.gov)
- •Completed active treatment of surgery, (neo)adjuvant chemotherapy, and/or (neo) adjuvant radiation. Patients receiving adjuvant endocrine therapy, targeted therapy, or immunotherapy therapies are eligible.
- •Ownership of a computer/tablet/smartphone with internet access.
- •Willingness to create a google account and maintain the account for use of the Fitbit
- •Willingness and ability to attend study visits.
- •Must be able to complete semi-tandem (10 seconds), side-by-side tandem [10 seconds and short physical performance batters(SPPB)] Score of 6 or greater to qualify for virtual exercise.
- •Must be ambulatory without the use of assisted device(s).
排除标准
- •Receiving surgery, (neo)adjuvant chemotherapy, (neo) adjuvant radiation, palliative treatment
- •Are already performing >150 minutes/week of moderate activity or 75 min/week of vigorous physical activity
- •Cancer-free for greater than 5 years
- •Unable to complete weekly interventions/exercise due to traveling or unable to be active for more than 7 consecutive days.
- •Squamous cell or basal cell skin cancers (melanoma still eligible)
- •Stage 0/in situ vulvar/cervical cancers
结局指标
主要结局
Rate of adherence to program based on participation in virtual exercise sessions
时间窗: Baseline; 12 weeks
Adherence evaluated based on participation in virtual exercise sessions during 12-week exercise intervention.
Change in Quality of Life (QOL) using Patient-Reported Outcomes Measurement Information System (PROMIS)
时间窗: Baseline; 12 weeks
QOL evaluated based on physical functioning and fatigue, assessed using Patient-Reported Outcomes Measurement Information System (PROMIS) pre- and post-12-week exercise intervention.
Change in physical functioning using Short Physical Performance Battery
时间窗: Baseline; 12 weeks
Change in physical functioning based on improvement in endurance, strength, and balance assessed using Short Physical Performance Battery (SPPB) pre- and post-12-week exercise intervention.
Change in satisfaction using a 5-point Likert scale
时间窗: Baseline; 12 weeks
Satisfaction assessed using a 5-point Likert scale following 12-week exercise intervention and participant-reporting likelihood of recommending program.
次要结局
未报告次要终点