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临床试验/NCT02475473
NCT02475473已完成不适用

Circulatory Levels of Irisin in Response to Chronic Resistance Training

Texas Tech University1 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2015年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
1
主要终点
Blood Lactate levels

研究概览

简要总结

Study the responses of circulatory irisin to chronic high-intensity resistance training

详细描述

Objective: The purpose of this study is to study the circulating levels of irisin in response to chronic high-intensity resistance training in a group of healthy young adults.

Sample: The sample will be comprised 44 of adult men and women unpaid volunteers between the ages of 18 and 30.

Pre-screening assessments:

Informed consent, PAR-Q, Medical History and Exercise History will be used to determine health status and prior exercise experience. Menstrual cycle log will be required for female participants.

Pre-Intervention assessments:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 30 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Exclusion Criteria:
  • •Known health problems such as cardiovascular, pulmonary or metabolic disease will be excluded.
  • •Pregnant females.
  • •Any adults found taking medications that affect endocrine or cardiovascular function will also be excluded from the study.
  • •Individuals found to be less than 110 pounds.
  • •Participants that exercise more than three times per week or strength train more than twice per week.
  • •Individuals that have poor venous access or have expressed a fear of needles or having blood taken will also be excluded.
  • •Cigarette smoking (current or those who quit within the previous 6 months
  • •Hypertension
  • •Overweight and obese
  • •Pre-diabetics

排除标准

  • •Known health problems such as cardiovascular, pulmonary or metabolic disease will be excluded.
  • •Pregnant females.
  • •Any adults found taking medications that affect endocrine or cardiovascular function will also be excluded from the study.
  • •Individuals found to be less than 110 pounds.
  • •Participants that exercise more than three times per week or strength train more than twice per week.
  • •Individuals that have poor venous access or have expressed a fear of needles or having blood taken will also be excluded.
  • •Cigarette smoking (current or those who quit within the previous 6 months
  • •Hypertension
  • •Overweight and obese
  • •Pre-diabetics

研究组 & 干预措施

Intervention

Experimental

The acute intervention will consist of 1 session of training following the program:

Resistance Training Exercises. Each participant in the intervention group will perform resistance-training exercises in the form of a circuit. The circuit will consist of 10 repetitions per exercise of 7 exercises: leg press, bent-over row, bench press, squats, dumbbell jump squats with raises, dead-lifts and weighted abdominal crunches, with approximately 30 sec of rest in between each exercise (based on the estimated time needed to move from one position to the next). Initial intensity 6-7 of RPE and ending the set at 9-10. Each participant will move through the circuit 3 times, with 2 to 3 minutes of rest between each round.

干预措施: Exercise Training (Other)

Control

No Intervention

Control

结局指标

主要结局

Blood Lactate levels

时间窗: 3 weeks

Intensity of exercise on sessions 1, 3, 6 and 9

Changes in Hematocrit concentration

时间窗: Baseline and 3 weeks

Changes in physical fitness levels as meassured by 1RM (repetition maximum) and Cardio-respiratory maximal testing

时间窗: Baseline and 3 weeks

Physical Activity assessment: accelerometry

时间窗: 3 weeks

Changes in Body composition assessment: DEXA and anthropometry

时间窗: Baseline and 3 weeks

Changes in Blood glucose levels

时间窗: Baseline and 3 weeks

Diet assessment: 24 hour recall and Food Preference Questionnaire

时间窗: 3 weeks

Change in Serum irisin levels

时间窗: Baseline and 3 weeks

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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