Movement Simulation Techniques and Therapeutic Exercise in Young Nulliparous Women: A Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 45
- 试验地点
- 1
- 主要终点
- maximal pelvic floor muscle strength (measured in grams and with the phenix device)
研究概览
简要总结
Both motor imagery and action observation training, either alone or in combination with physical practice, have been shown to improve some clinical variables of interest such as strength and motor control. However, this has not yet been investigated in the pelvic floor musculature.
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
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 30 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Over 18 years of age and asymptomatic women.
排除标准
- •This study will exclude those who presented a respiratory pathology, cardiac, systematic, or metabolic disease, history of recent surgery, vertebral fracture, or osteoarticular disorders of the spine area.
研究组 & 干预措施
Therapeutic exercise plus motor imagery
干预措施: Therapeutic exercise plus motor imagery (Behavioral)
Therapeutic exercise plus action observation
干预措施: Therapeutic exercise plus action observation (Behavioral)
Therapeutic exercise
干预措施: Therapeutic exercise (Behavioral)
结局指标
主要结局
maximal pelvic floor muscle strength (measured in grams and with the phenix device)
时间窗: pre-intervention (T0), at one week after the intervention (T1) and at two weeks after starting the intervention (post-intervention (T2)).
Three measurements of maximal pelvic floor strength shall be performed with an intracavitary probe and the mean of the three measurements of maximal pelvic floor muscle strength shall be considered.
Motor control of the lumbopelvic area assessed with a biofeedback device.
时间窗: pre-intervention (T0), at one week after the intervention (T1) and at two weeks after starting the intervention (post-intervention (T2)).
A protocol to assess lumbopelvic dissociation (i.e. moving the legs without moving the lower back) of both legs of the participants will be performed with a biofeedback device that assesses the pressure exerted on the lower back during leg mobilisation (in mmHg).
Algometry for assessing pressure pain thresholds (Pain sensitivity)
时间窗: pre-intervention (T0), at one week after the intervention (T1) and at two weeks after starting the intervention (post-intervention (T2)).
An algometer shall be used to assess pain thresholds to pressure, i.e. squeezing so that pressure is converted into pain at four points. Two points in the symphysis pubis area, one point in the lumbar area and one point near the tibial tuberosity.
次要结局
未报告次要终点
研究者
Ferran Cuenca
Principal investigator
University of Valencia