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临床试验/NCT07576894
NCT07576894招募中不适用

Phenotyping Resting and Exertional Right Ventricular Dysfunction Among Patients With Chronic Obstructive Pulmonary Disease

University of Colorado, Denver1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年8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
招募中
入组人数
60
试验地点
1
主要终点
Right ventricular contractility measured by transthoracic echocardiography

研究概览

简要总结

This study plans to learn more about heart function among individuals with chronic obstructive pulmonary disease (COPD). In particular, the investigators want to understand the different patterns of right ventricular response during rest and moderate- vs high-intensity exercise. By identifying patterns of right ventricular dysfunction, this study will help identify better treatments for patients with COPD in the future.

详细描述

This study will determine patterns of right ventricular (RV) response to aerobic exercise in patients with chronic obstructive pulmonary disease (COPD) and will design a targeted exercise intervention to improve RV response. We will study 60 patients with COPD. Participants will complete cardiopulmonary exercise testing (CPET) and transthoracic echocardiography (TTE) during rest, moderate- and high-intensity exercise. A subset of participants (n=16) who have been recommended to undergo clinical right heart catheterization will be recruited for the primary study with additional invasive pressure-volume analysis during the CPET. This testing will be used to validate measures of RV function obtained through noninvasive testing. The sample size was selected based upon our preliminary data and statistical analysis plans.

To test whether an exercise intervention targeted to RV response to exercise is feasible for patients, 12 participants will complete a targeted exercise training intervention based on their RV contractile response during baseline testing. This intervention will include participants who demonstrate RV contractility increase to moderate- but not high-intensity exercise. We will test the feasibility of a moderate-intensity interval training program. Participants will complete exercise training sessions 3x/week for 12 weeks. Exercise training will be performed on an upright stationary bicycle. Following the exercise training intervention, participants will repeat CPET and TTE. They will also complete a health-related quality of life questionnaire before and after the exercise training intervention.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • •COPD (determined by ratio of forced expiratory volume in 1 second to forced vital capacity [FEV1/FVC] <0.7)
  • •Age >= 40 years

排除标准

  • •Exacerbation of COPD in the 3 months prior to enrollment
  • •Change in COPD therapy in the 3 weeks prior to enrollment
  • •Requirement of >6 LPM supplemental oxygen at rest
  • •Requirement of >10 LPM supplemental oxygen with exertion
  • •Active/uncontrolled cardiovascular disease (e.g. hypertension with blood pressure >150/100 despite antihypertensives; coronary artery disease with angina; left ventricular ejection fraction ≤40%; uncontrolled arrhythmia; pulmonic, mitral or aortic valvular abnormality greater than mild in severity; tricuspid regurgitation greater than moderate in severity)
  • •Volume overload (jugular vascular distension or greater than trace peripheral edema)
  • •World Health Organization Functional Class IV
  • •Known pulmonary hypertension with mean pulmonary artery pressure >45 mmHg
  • •Untreated severe obstructive sleep apnea and/or obesity hypoventilation syndrome
  • •Active malignancy (other than skin)
  • •Medical conditions that limit exercise on an upright stationary bicycle (e.g. severe osteoarthritis, imbalance/gait instability, etc.)
  • •Pregnancy
  • •Body mass index <18 or >35
  • •Hematocrit <25% or >55%
  • •For subset undergoing right heart catheterization, chronic anticoagulation that is unable to be held for the study visit
  • •For subset undergoing right heart catheterization or exercise training, forced expiratory volume in 1 second of <20%
  • •For exercise training, already engaged in routine exercise training (>30 minutes at >3 METs 3 times/week or more)
  • •For exercise training, inability to complete initial in-person exercise training sessions for approximately 35 minutes 3x/week for 3 weeks (followed by exercise training sessions with an option for hybrid remote/in-person participation)
  • •For exercise training with an option for hybrid remote exercise training, any medical conditions which threaten the safety of remote exercise training (e.g. imbalance/gait instability, etc.).

研究组 & 干预措施

COPD

Experimental

Participants will complete testing at rest and during moderate- and high-intensity exercise to identify patterns of right ventricular responses. Participants who based on baseline testing are eligible and decide to participate in the optional exercise training program will complete exercise training followed by repeat testing to determine the impact of exercise training on right ventricular dysfunction.

干预措施: Exercise training (Behavioral)

结局指标

主要结局

Right ventricular contractility measured by transthoracic echocardiography

时间窗: Up to 1 hour

Global longitudinal strain, measured in absolute percent

次要结局

  • Right ventricular contractility measured by conductance catheter(Up to 1 hour)
  • Right ventricular systolic function measured by transthoracic echocardiography(Up to 1 hour)
  • Exercise training safety(4 months)
  • Exercise training feasibility(4 months)
  • Health-related quality of life by Short Form 36 (SF-36) questionnaire(Up to 1 hour)
  • Maximum oxygen consumption (VO2max)(Up to 1 hour)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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