Nighttime Feeding and Morning Endurance Performance
Effect of Nighttime Feeding on Morning Performance in Female Endurance Athletes
研究概览
详细说明
This study will be interventional in nature and employ a crossover, randomized, double-blinded approach. This study will include a maximal oxygen uptake test and three trials: one familiarization trial, and two experimental trials. The familiarization will serve as a practice test to minimize any training effects between experimental trials. The experimental trials will be completed within a 2-week period determined by the luteal phase of the menstrual cycle (days 15-28 of the menstrual cycle, with day 1 being the first day of menstruation). A minimum of 48-72 hours will be provided between testing days.
Experimental trials will consist of baseline testing (height, weight, urinalysis, resting metabolic rate), followed by a treadmill performance protocol. Participants will complete a 3-stage incremental exercise test (at 55%, 65%, and 75% of maximal oxygen uptake respectively). Metabolic data will be collected during this time. Participants will then complete a 10-kilometer running time trial in which markers of intensity are monitored at various time points (blood glucose, blood lactate, heart rate, rating of perceived exertion). Participants and primary researchers will be blinded to all time and speed data. Distance will be the only known measure of progress. Additional blood, urine, and body weight measures will be taken immediately post exercise.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
Florida
-
Tallahassee、Florida、美国、32306
- Florida State University
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Female
- Between the ages of 18 and 40 years old
- Consistently use oral contraceptives (greater than 2 months) or be considered eumenorrheic without oral contraceptive use
- 'Moderately trained,' defined as a weekly mileage ≥ 25 miles for at least 6 months, and a VO2max ≥ 45 ml/kg/min
Exclusion Criteria:
- Lactose intolerant
- Smokers
- Uncontrolled thyroid conditions
- Uses anti-inflammatory drugs or any dietary supplements intended to improve performance
- Have musculoskeletal injury that could limit performance
学习计划
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:双倍的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:chocolate milk
In this arm, subjects receive chocolate milk
|
12 oz, 7-8 hours prior to exercise trial (night before)
|
|
安慰剂比较:flavor-matched placebo
In this arm, subjects receive a flavor-matched placebo
|
12 oz, non-caloric flavor-matched placebo
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Running Performance
大体时间:24 hours
|
10K time trial on a treadmill
|
24 hours
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Urine Specific Gravity
大体时间:24 hours
|
Changes in urine specific gravity will be measured pre and post a 10K time trial run on a treadmill
|
24 hours
|
|
Urine Volume
大体时间:24 hour
|
Measurement of total urine output.
|
24 hour
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Exercise Metabolism
大体时间:24 hours
|
Indirect calorimetry will be used to assess macronutrient use during exercise via the respiratory exchange ratio
|
24 hours
|
合作者和调查者
调查人员
- 首席研究员:Michael J Ormsbee, PhD、Florida State University
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- CHMK-1415
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.