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临床试验/NCT06992414
NCT06992414尚未招募不适用

Exploring Creatine Supplementation for Improved Exercise Capacity and Reduced Fatigue in Long COVID-19: A Randomized Controlled Trial

University of Calgary0 个研究点目标入组 24 人开始时间: 2025年7月2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
24
主要终点
Oxygen consumption at ventilatory threshold

研究概览

简要总结

Individuals living with Long COVID often experiencing a degree of undue fatigue after physical or cognitive exertion secondary to the condition, timed post-exertional malaise 9PEM). This trial aims to explore the efficacy of creatine monohydrate in managing PEM

详细描述

cognitive dysfunction, and post-exertional malaise are common complaints of those living with Post-COVID Condition (PCC), a sequelae of symptoms that persist beyond acute infection. Similar to other types of post-viral fatigue, the diagnosis and treatment of PCC are challenging due to the lack of a valid biomarker for the condition. Though the etiology of PCC is not well understood, recent research has found reduced skeletal muscle creatine concentration in those with PCC, which may contribute to fatigue. The objective of this study is to determine if eight weeks of creatine monohydrate supplementation (8g/day) improves symptoms of fatigue, cognition, exercise capacity, and PEM in individuals living with PCC.

Participants will complete two cardiopulmonary exercise tests 24-hours apart on a cycle ergometer before and after an eight-week intervention period. Venous blood samples will be collected before and after exercise on both days to assess changes in mitochondrial function. During the intervention, participants will be randomly assigned to supplement with 8g/day of either creatine monohydrate or a control (maltodextrin). Cognition will be indirectly assessed via self-report of cognitive symptom frequency and severity at baseline, mid-intervention (i.e., 4 weeks) and post-intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • •Experiencing symptoms at least 3 months after a COVID-19 diagnosis confirmed by positive polymerase chain reaction (PCR) test
  • •Experiencing post-exertional malaise, as per the DePaul Symptom Questionnaire

排除标准

  • •Allergy or intolerance to creatine monohydrate or maltodextrin
  • •Supplemented with creatine in the past eight weeks
  • •orthopaedic injury or condition that would prevent exercise testing
  • •change in medication related to Long COVID symptom management in the past month.

研究组 & 干预措施

Creatine monohydrate

Experimental

8 g/day creatine monohydrate

干预措施: Creatine monohydrate (Dietary Supplement)

Maltodextrin

Placebo Comparator

8 g/day maltodextrin

干预措施: Creatine monohydrate (Dietary Supplement)

结局指标

主要结局

Oxygen consumption at ventilatory threshold

时间窗: From enrollment to the end of intervention at 8 weeks

point of respiratory compensation point (i.e., ventilatory threshold 2) as a percent of maximal oxygen consumption

Heart rate at ventilatory threshold

时间窗: From enrollment to the end of intervention at 8 weeks

heart rate (in bpm) at point of ventilatory threshold

次要结局

  • Fatigue(From baseline to mid intervention (4 weeks) to the end of the intervention (8 weeks))
  • Brain fog(From baseline to mid intervention (4 weeks) to post intervention (8 weeks))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Keely Shaw

Postdoctoral Associate

University of Calgary

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