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临床试验/NCT06686238
NCT06686238尚未招募不适用

Acute Effects of a Hypoxia-hyperoxia Exposure Session on Sedentary Older Adults on Heart Rate Variability, Blood Pressure, and Oxygen Saturation, a Randomized Double-blind Placebo-controlled Clinical Trial

Sierra Varona SL1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2024年12月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
16
试验地点
1
主要终点
Heart rate variability

研究概览

简要总结

The supply of oxygen is essential for energy production, recovery from efforts, and human life. Intermittent Hypoxia-Hyperoxia Exposure (IHHE) is a novel technique in which the subject is exposed to a respiratory environment with reduced oxygen fraction, controlled through a specific software, using a facial mask and a hypoxic generation device. The objective of this study is to determine if there is a relationship between intermittent hypoxia-hyperoxia exposure and cardiorespiratory condition, blood pressure, and arterial oxygen saturation.

According to our hypothesis, acute IHHE in elderly adults may influence cardiorespiratory condition, blood pressure, and arterial oxygen saturation.

The study will be conducted as a randomized clinical trial. The subjects will be divided into two groups: the experimental group will undergo an IHHE session, breathing air with an oxygen concentration (FiO2) ranging from 10-14% for 1-5 minutes, with 1-3 minutes of rest in hyperoxia (FiO2 30-40%) for a total of 4-8 cycles, based on their acute response to hypoxia. The placebo group will undergo a 5-cycle protocol with an FiO2 of 21%.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
65 Years 至 90 Years(Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Being over 60 years old.
  • •Having no previous experience in hypoxic training.
  • •Engaging in less than 150 minutes of physical activity per week.

排除标准

  • •Having any pathology that prevents the subject from being independent in terms of walking and functionality.
  • •Subjects with impaired cognitive abilities.
  • •Subjects with pulmonary hypertension, decompensated heart or respiratory disease.
  • •To have or have had cancer

研究组 & 干预措施

Hypoxic-Hyperoxic group

Experimental

The EG (Experimental Group) will undergo a single session of IHHE (Intermittent Hypoxia-Hyperoxia Exposure) session using the MITOVIT® Hypoxic Training System (COMMIT GmbH, Salzgitter, Germany). They will breathe air with an oxygen concentration (FiO2) ranging from 10-14% for 5 minutes, followed by 3 minutes of rest in hyperoxia (FiO2 30-40%), for a total of 6 cycles. During the hypoxic phase, oxygen saturation will be maintained between 85-92%, while during the hyperoxic phase, it will be kept above 95%. This process is regulated by the device's AI.

Participants will be asked to sit and breath normally in each exposure.

An attendance checklist will be used to monitor compliance with the intervention

干预措施: MITOVIT® Hypoxic Training System (Device)

Sham Hypoxic-Hyperoxic Group

Sham Comparator

The Sham Group (SG) will follow a single session protocol of 5 cycles of 6 minutes per session with an FiO2 of 21% using the MITOVIT® Hypoxic Training System (COMMIT GmbH, Salzgitter, Germany).

Participants will be asked to sit and breath normally in each exposure.

An attendance checklist will be used to monitor compliance with the placebo intervention.

干预措施: Sham MITOVIT® Hypoxic Training System (Device)

结局指标

主要结局

Heart rate variability

时间窗: Immediately before intervention and immediately after intervention

The analysis of Heart Rate Variability will be conducted using a heart rate monitor. Cardiac electrical signals will be monitored with a band placed on the chest for 5 minutes with the subject in supine position on a stretcher, in a quiet environment, soft light, and a comfortable temperature. Subjects are instructed not to speak or make voluntary movements during this analysis.

次要结局

  • Blood pressure(Immediately before intervention and immediately after intervention)
  • Arterial oxygen saturation(Immediately before intervention and immediately after intervention)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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