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临床试验/NCT04954222
NCT04954222已完成不适用

Tracking the Recovery of Respiratory Physiology in COVID-19 Patients a Pilot Study

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2022年2月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Mayo Clinic
入组人数
80
试验地点
2
主要终点
change in quality of life

研究概览

简要总结

The purpose of this study is to determine the effects of the clinical course of treatment as well as long-term symptoms of COVID-19 on respiratory function, exercise capacity, and quality of life.

详细描述

This study will be completed over 4 sessions at the Mayo Clinic at either the Scottsdale Arizona or Rochester Minnesota locations. You will be asked to complete a series of questionnaires, lung function tests, and exercise tests at two time points: ≥ 28 days post diagnosis and 4-6 months after the first laboratory visit. All visits will take approximately 2 hours. During visits 1 and 3 a series of questionnaires as well as breathing tests, and an exercise test will be completed on a stationary bike. You will also be asked to breathe a gas mixture out of a bag to obtain measures of gas movement and sensitivity. During visits 2 and 4 you will complete an exercise test on a stationary bike to measure changes from the previous exercise test and a chest scan.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Have a documented positive qRT-PCR for SARS-CoV-2 confirming prior COVID-19 diagnosis
  • At least 18 years of age.
  • Female subjects must not be pregnant or trying to become pregnant during the duration of study participation.
  • No known plans to move out of the state, or become unable to return to one of the Mayo Clinic sites for follow-up testing.
  • Must be able to provide clear informed written consent.

排除标准

  • Individuals with pacemakers or other implantable devices that will make interpreting a CT scan challenging.
  • Individuals with major limitations to exercise.

结局指标

主要结局

change in quality of life

时间窗: through study completion, an average of 5 months

SF-36 questionnaire assessment of physical and mental health. Two scores one for physical functioning and one for mental functioning. Scores range from 0-100 with a higher score indicating better health

Change in diffusion capacity of the lungs

时间窗: through study completion, an average of 5 months

change in diffusing capacity of the lungs for carbon monoxide and its components

Presence of post-exertional malaise

时间窗: through study completion, an average of 5 months

Evaluation of change in performance on maximal exercise test over two days to identify presence of post-exertional malaise

change basic spirometry

时间窗: through study completion, an average of 5 months

Measurement of basic lung function using forced vital capacity (FVC), slow vital capacity (SVC), forced expiratory volume at one second (FEV1), maximal inspiratory pressure (MIPS), maximal expiratory pressure (MEPS), exhaled nitric oxide (ExNO), forced oscillation technique (FOT), overnight pulse oximetry

Change in symptoms

时间窗: through study completion, an average of 5 months

St. George's respiratory Questionnaire scoring of pulmonary symptoms. Scores range from 0 to 100, with higher scores indicating more limitations.

Change in airway morphology

时间窗: through study completion, an average of 5 months

CT assessment of airway diameter and thickness

Change in peak aerobic capacity

时间窗: through study completion, an average of 5 months

Change in examine post exertional malaise

次要结局

未报告次要终点

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Courtney M. Wheatley

Co-Principal Investigator

Mayo Clinic

研究点 (2)

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