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临床试验/NCT04526184
NCT04526184Unknown不适用

Systemic Effects of A Continuous Blood Flow Restricted Aerobic Exercise Session in COPD Patients: A Randomised Controlled Trial.

Medipol University2 个研究点 分布在 2 个国家目标入组 46 人开始时间: 2020年8月17日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
46
试验地点
2
主要终点
oxidative stress markers

研究概览

简要总结

Patients with COPD that a pulmonologist classifies between Stage 1-2 in accordance with the GOLD criteria and age and gender-matched healthy individuals will be included in the study.

In both groups (n = COPD: 17, Healthy: 17), aerobic exercise (AE) in the target heart rate range of 50% intensity, performed by cycling accompanied by blood flow restriction, will be applied.

详细描述

Target heart rate will be calculated from the formula "(Maximal heart rate-resting heart rate) x% desired intensity ratio + resting heart rate".

The target occlusion amount in the lower extremity will be calculated by calculating 45% of the complete occlusion rates reported by Michael et al. The proximal border of the thigh cuffs will be tied in line with the gluteal lines on both sides.

Exercise tolerance and dyspnea condition; Measurement properties in COPD will be evaluated using a well-defined modified Borg scale (MBS). Individuals will use any bronchodilator that their doctor sees fit before trying.

The target aerobic exercise intensity will be reached in the last minute of the first five-minute warm-up period by maintaining a 4-6 feeling of dyspnea in the MBS, by increasing pedal resistance and speed. In case of extreme shortness of breath, exercise intensity will be reduced to resting heart rate.

In the event of oxygen desaturation (85%) during the intervention, the intervention will be terminated.

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)

盲法说明

25 COPD patients were referred to the study from the pulmonology clinic of the hospital where the study was conducted by a medical secretary who was blinded to the intervention. In addition, 21 healthy individuals volunteered to participate in the study from the same hospital where the study was previously announced.

入排标准

年龄范围
40 Years 至 75 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • No drug change for at least 30 days for the COPD group
  • Not participating in a structured activity program for at least six months
  • Have the ability to cooperate

排除标准

  • Presence of any pathology that limits physical activity performance
  • Presence of severe or unstable heart disease
  • Presence of peripheral artery disease
  • Being in an exacerbation period of the disease
  • Presence of another active disease (rheumatic, oncological, traumatic etc.)
  • Any neurological or orthopedic disease that prevents exercise

研究组 & 干预措施

healthy group

Active Comparator

25 healthy individuals between the ages of 40-70 will be contacted by phone and included in the initiative.

干预措施: aerobic exercise with blood flow restriction (Procedure)

patient group

Active Comparator

25 individuals will be selected randomly from 103 patients with COPD from hospital records.

干预措施: aerobic exercise with blood flow restriction (Procedure)

结局指标

主要结局

oxidative stress markers

时间窗: up to 18 weeks

uric acid, lactate dehydrogenase

creatine kinase

时间窗: 30 minutes

rhabdomyolysis marker

C reactive protein, neutrophil

时间窗: 30 minutes

inflammatory marker

modified borg scale

时间窗: up to 18 weeks.

dyspnoea measurement, Minimum 1, maximum 7 points are obtained. 5 indicates the best respiratory condition, 10 the worst respiratory condition.

heart rate

时间窗: 30 minutes

determination of aerobic exercise dose

oxygen saturation

时间窗: 30 minutes

blood oxygen saturation

systolic and diastolic pressure

时间窗: up to 18 weeks

to mean arterial pressure calculation

次要结局

未报告次要终点

研究者

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

Ahmet Gunes

PhD Student

Medipol University

研究点 (2)

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