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临床试验/NCT01812590
NCT01812590已完成不适用

Acute Exercise and Pancreatic Endocrine Function

Rigshospitalet, Denmark1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2013年1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
14
试验地点
1
主要终点
Pancreatic endocrine function

研究概览

简要总结

Subjects with type 2 diabetes will be stratified into two-quantiles based on ambient hyperglycemia (fasting glucose and HbA1c) and then the effects of a single aerobic exercise bout (1-hour at 50%VO2max) on pancreatic endocrine function will be determined.

研究设计

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

入排标准

年龄范围
30 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Previous diagnosis with type 2 diabetes, or newly detected in our screening procedures
  • •Age 30-70 years
  • •BMI 20-40 kg/m2

排除标准

  • •Treatment with insulin
  • •Contraindication to exercise as determined by ECG
  • •Pregnancy
  • •Active weight loss in the previous 6 months
  • •Actively engaged in exercise training programs
  • •Evidence of chronic pulmonary, cardiovascular, hepatic, renal, or hematological disease

研究组 & 干预措施

Resting Trial

No Intervention

Pancreatic endocrine function will be determined the morning following a day where no exercise is performed

Exercise Trial

Experimental

Pancreatic endocrine function will be determined the morning following a day where a 1-hour aerobic exercise is performed at 65% of pre-determined HRmax (maximal heart rate measured during an incremental work-load exercise test to volitional exhaustion)

干预措施: Exercise (Behavioral)

结局指标

主要结局

Pancreatic endocrine function

时间窗: 24-hours following a period of rest/exercise

Insulin and glucagon secretory responses to intravenous glucose (hyperglycemic clamp 5.4 mmol/l above basal), glucagon-like peptide-1 (0.5 pmol/kg/min), and arginine (5 g injection) will be determined.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thomas Solomon

Senior Researcher

Rigshospitalet, Denmark

研究点 (1)

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