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临床试验/NCT06379204
NCT06379204已完成不适用

A Study on the Intervention of Metabolic Syndrome Patients With Exercise Prescription Based on Ventilatory Threshold Using Cardiopulmonary Exercise Test

Taiyuan Central Hospital of Shanxi Medical University1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2022年11月4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
发起方
入组人数
52
试验地点
1
主要终点
Peak oxygen uptake

研究概览

简要总结

Analyze the clinical intervention effects and differences of progressive precision exercise prescriptions formulated by two methods for determining exercise intensity on metabolic syndrome (MS). Compare the effects of the two on the cardiovascular endurance of the MS population and verify the effectiveness of individualized methods in reducing absolute exercise intensity for MS patients.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
25 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients were included who met the Chinese Diabetic Society diagnostic criteria for MS-i.e., three or more of the following five items: (i) abdominal obesity (i.e., central obesity) with waist circumference ≥ 90 cm in males and ≥ 85 cm in females; (ii) hyperglycemia defined as fasting blood glucose ≥ 6.1 mmol/L or blood glucose ≥ 7.8 mmol/L two hours after glucose loading, or diagnosis of diabetes mellitus; (iii) hypertension defined as blood pressure ≥ 130/85 mmHg or diagnosed with hypertension; (iv) fasting triglycerides (TG) ≥ 1.70 mmol/L; and (v) fasting high-density lipoprotein cholesterol (HDL-C) < 1.04 mmol/L.
  • •Patients were aged 25 to 65 years, with no restrictions on number of males or females.
  • •Patients exhibited a long-term sedentary lifestyle and did not carry out moderate-intensity physical activity for at least three d/week of 30 min/d duration within three months of the study.
  • •Patients were willing to participate and sign the informed consent form.

排除标准

  • •Patients in an acute phase of various diseases or with organ failure, tumor, myocardial infarction, cardiac insufficiency, myocarditis, or chronic lung disease;
  • •Patients with long-term alcohol consumption and those unable to ensure regular lifestyle habits during the intervention period;
  • •Patients who were unable to ensure that they would carry out the stipulated exercise protocol during the intervention; and
  • •Patients with drug modifications during the intervention that could affect the outcome markers.

研究组 & 干预措施

the maximum physiological value standardized group

Experimental

干预措施: the maximum physiological value standardized group (Behavioral)

the ventilatory threshold individualized group

Active Comparator

干预措施: the ventilatory threshold individualized group (Behavioral)

结局指标

主要结局

Peak oxygen uptake

时间窗: From enrollment to the end of 12 weeks of treatment

次要结局

未报告次要终点

研究者

发起方
Taiyuan Central Hospital of Shanxi Medical University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Liu Ruojiang

Chief Therapist

Taiyuan Central Hospital of Shanxi Medical University

研究点 (1)

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