Effectiveness of an 8-week Independent Cadence Retraining Program on Stress Urinary Incontinence in Parous Runners: A Randomized Controlled Trial.
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- Mayo Clinic
- 入组人数
- 66
- 试验地点
- 1
- 主要终点
- Preferred Cadence
研究概览
简要总结
The purpose of this research is to assess the impact of an eight-week home cadence training program on stress urinary incontinence symptoms in parous women.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Nonpregnant
- •Female volunteers
- •Self-reported urinary incontinence during running with history of at least one prior delivery after 32 weeks gestation and who run 6 miles/week with a preferred cadence of less than or equal to 170 steps per minute determined via personal report from current Garmin watch data.
- •Participants must own their own or have access to a Garmin watch.
- •Participants must read, speak, and understand English sufficiently to provide informed consent and complete study procedures and questionnaires.
排除标准
- •Unwillingness to complete all components of the study
- •Urge only urinary incontinence
- •<3 months postpartum or current pregnancy
- •History of prolapse repair or incontinence surgery
- •Participants will also be excluded if they do not own or utilize a Garmin watch that provides cadence assessment and alarm.
研究组 & 干预措施
Cadence increase group
Participants will log running data and set cadence alarms to increase running cadence by 10%
干预措施: Cadence Increase (Other)
Cadence Maintenance Arm
Participants will log their running data and set cadence alarm to maintain cadence.
干预措施: Cadence Maintenance (Other)
结局指标
主要结局
Preferred Cadence
时间窗: Intake and 8 weeks
Participants will self-assess preferred running cadence using a garmin device during a 15 minute self-paced run.
PFDI-20
时间窗: Intake, 8 weeks, and 6 month
questionnaire that assesses bowel, bladder, and pelvic symptoms and their impact on quality of life.
QUID
时间窗: intake, 8 weeks, and 6 months
6 item urinary incontinence questionnaire
ICIQ-UI
时间窗: intake, 8 weeks, and 6 months
Self reported, short and simple tool to evaluate the frequency, severity and impact of urinary incontinence in men and women
Global Rating of Change
时间窗: 8 weeks and 6 months
Scale allowing patient to self-report perceived change of UI symptoms
次要结局
未报告次要终点