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临床试验/NCT07419100
NCT07419100尚未招募不适用

From Sitting to Moving: How Physical Activity Patterns Can Reduce Sedentary Behaviour and Support Cardiometabolic Health

Hasselt University1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2026年3月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
48
试验地点
1
主要终点
Total and incremental area under the curve of postprandial insulin response

研究概览

简要总结

According to the World Health Organization (WHO), chronic diseases are a major global public health concern and the leading cause of mortality worldwide. In the absence of evidence-based actions, the global annual deaths from chronic diseases are projected to rise to 55 million deaths in 2030, accompanied by a substantial increase in socio-economic costs. In this context, the WHO identifies type 2 diabetes mellitus (T2DM) and cardiovascular diseases (CVD) as key chronic conditions of concern related to cardiometabolic health.

Both sedentary behaviour (SB) and physical inactivity have been recognised as interdependent risk factors for the development of T2DM and CVD. SB refers to any waking behaviour, characterised by a low energy expenditure, while being in a sitting or reclining posture, whereas physical inactivity denotes insufficient levels (<150 min per week,) of moderate-to-vigorous physical activity (MVPA). Studies using objective measures have demonstrated that on average Western adults spend 8-12h in SB per day, of which the majority is spent in prolonged sedentary bouts (lasting ≥30 min). In addition, up to 30% of adults worldwide are physically inactive, with higher levels of inactivity in high-income countries. Within this context, it has become evident that excessive prolonged SB, often in combination with physical inactivity, negatively impacts cardiometabolic health, contributing to insulin resistance, increased adiposity, poor lipid profiles and endothelial dysfunction. Given their detrimental effects on T2DM and CVD, strategies aimed at reducing SB and promoting physical activity (PA) warrant further investigation.

Reducing and regularly interrupting SB, even with low-intensity PA, alongside sufficient MVPA, is crucial for maintaining a healthy cardiometabolic profile. Reflecting this, the WHO guidelines advise individuals to engage in 150-300 minutes of moderate-intensity physical activity, 75-150 minutes of vigorous-intensity physical activity, or an equivalent combination each week. Notably, the 2020 WHO guidelines also included recommendations on SB for the first time, emphasizing the importance of limiting sedentary time. The WHO states that replacing SB with physical activity of any intensity can yield health benefits. However, these recommendations remain non-prescriptive and somewhat vague, primarily due to a lack of robust scientific evidence on the optimal frequency, intensity, and duration of PA needed to interrupt sedentary time. The absence of specific guidelines on prolonged SB reflects this evidence gap. To support policy development, well-designed randomised controlled trials are needed to evaluate effective and practical strategies for reducing sedentary time.

So far, the short term cardiometabolic health effects of SB interruptions have been investigated by our research group, laboratory studies of collaborators and other international researchers, demonstrating that; 1) more frequent SB interruptions especially affect glucose metabolism and insulin sensitivity; 2) higher intensity interruptions are associated with cardioprotective adaptations and; 3) longer durations of SB interruptions positively affect lipid metabolism. However, because under real-world conditions frequency, intensity and duration of SB interruptions usually interact, their combined effects on cardiometabolic health need further investigation. Many studies already compared the isolated effects of different SB interruption patterns with respect to frequency, duration and intensity on cardiometabolic health. However, the combined effects of these different approaches matched for energy expenditure are not clear yet. We therefore perform a balanced cross-over study in which the efficacy of distinct activity patterns on cardiometabolic health insulin sensitivity and vascular function) will be compared to a sedentary control condition.

研究设计

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

入排标准

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

入选标准

  • Adults aged 40-70 years
  • Sedentary (>9 hours per day)
  • < 3 exercise sessions per week

排除标准

  • Pregnancy or intend to become pregnant
  • Any known contra-indications for physical activity
  • >14 alcohol consumptions per week for women and >20 alcohol consumptions per week for men
  • Involved in a weight reduction program with an energy restriction diet during the study period
  • No consistent body weight over the past month
  • Diagnosed with any known cardiometabolic health-related disease

研究组 & 干预措施

Control

No Intervention

Prolonged sitting for 6 hours

Continuous moderate intensity physical activity

Experimental

One continuous physical activity bout of moderate intensity will be performed during the 6 hour testing day.

干预措施: Continuous moderate intensity physical activity (Behavioral)

Continuous moderate intensity physical activity + light-intensity physical activity breaks

Experimental

One continuous physical activity bout of moderate intensity will be combined with light-intensity physical activity breaks every 30 minutes during the 6 hour testing day.

干预措施: Continuous moderate intensity physical activity (Behavioral)

Continuous moderate intensity physical activity + light-intensity physical activity breaks

Experimental

One continuous physical activity bout of moderate intensity will be combined with light-intensity physical activity breaks every 30 minutes during the 6 hour testing day.

干预措施: Light-intensity physical activity breaks (Behavioral)

Continuous moderate intensity physical activity + high-intensity physical activity breaks

Experimental

One continuous physical activity bout of moderate intensity will be combined with high-intensity physical activity breaks every 30 minutes during the 6 hour testing day.

干预措施: Continuous moderate intensity physical activity (Behavioral)

Continuous moderate intensity physical activity + high-intensity physical activity breaks

Experimental

One continuous physical activity bout of moderate intensity will be combined with high-intensity physical activity breaks every 30 minutes during the 6 hour testing day.

干预措施: High-intensity physical activity breaks (Behavioral)

Light-intensity physical activity breaks

Experimental

Prolonged sitting will be interrupted by light-intensity physical activity breaks every 30 minutes during the 6-hour testing day.

干预措施: Light-intensity physical activity breaks (Behavioral)

High-intensity physical activity breaks

Experimental

Prolonged sitting will be interrupted by high-intensity physical activity breaks every 30 minutes during the 6-hour testing day.

干预措施: High-intensity physical activity breaks (Behavioral)

结局指标

主要结局

Total and incremental area under the curve of postprandial insulin response

时间窗: Blood samples will be collected at 0, 30, 60, 120, 180, 210, 240, 300, and 360 minutes during the 6-hour testing day.

Insulin concentrations will be assessed in serum samples at nine time points over the 6-hour testing period. Postprandial responses will be quantified as the area under the curve (AUC) across the six-hour period.

Vascular endothelial function

时间窗: FMD measurement will be performed at the start (08:30 a.m.) and after 6 hours (2:30 p.m.) of the testing day.

Vascular endothelial function will be assessed by flow-mediated dilation (FMD) according to published guidelines. These measurements take place at 8 a.m. and involve doppler ultrasound imaging of the superficial femoral artery. A cuff will be placed on the right lower leg, and the superficial femoral artery is imaged longitudinally. FMD will be measured at baseline and after a 5-min occlusion phase (reactive hyperaemia response). FMD will be quantified as the percentage difference between peak and baseline diameter (FMD%).

次要结局

  • Total cholesterol concentration(Blood samples will be taken at the beginning of the testing day (8 a.m.).)
  • Cardiorespiratory Fitness(Baseline measurement)
  • Sedentary time(Measured for 7 consecutive days after the screening visit)
  • Body mass index(Baseline measurement)
  • Moderate-to-vigorous physical activity(Measured for 7 consecutive days after the screening visit)
  • Body weight(Baseline measurement)
  • High-density lipoprotein cholesterol concentration(Blood samples will be taken at the beginning of the testing day (8 a.m.).)
  • Total and incremental area under the curve of postprandial glucose response(Blood samples will be collected at 0, 30, 60, 120, 180, 210, 240, 300, and 360 minutes during the 6-hour testing day.)
  • Total and incremental area under the curve of postprandial insulin response(Blood samples will be collected at 0, 30, 60, 120, 180, 210, 240, 300, and 360 minutes during the 6-hour testing day.)
  • Peak heart rate(Baseline measurement)
  • Blood pressure(Blood pressure will be measured during the screening visit, and hourly at 0, 60, 120, 180, 240, 300, and 360 minutes during the 6-hour testing day.)
  • Body fat percentage(Baseline measurement)
  • Low-density lipoprotein cholesterol concentration(Blood samples will be taken at the beginning of the testing day (8 a.m.).)
  • Waist circumference(Baseline measurement)

研究者

发起方
Hasselt University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Bert Op't Eijnde

Professor

Hasselt University

研究点 (1)

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