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临床试验/NCT02076334
NCT02076334已完成不适用

Effect of Compression Garments on Exercise Performance Following Acute High Intensity Exercise

University of North Carolina, Chapel Hill1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2014年2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
已完成
入组人数
84
试验地点
1
主要终点
Maximal Voluntary Contraction (MVC)

研究概览

简要总结

To examine the influence of compression garments manufactured with Far-Infrared technology on exercise performance during and after repeated eccentric isokinetic muscle actions of the leg extensors.

详细描述

Participants: Eighty recreationally active (1-5 hrs per week) healthy participants between the ages of 18 - 35 will visit the Neuromuscular Research Laboratory on 6 separate occasions, with 4 of those occasions also requiring a visit to Health services for a blood draw.

Procedures (methods): During pre-screening, each participant will complete an informed consent document, a health history questionnaire, and have their stature and body mass assessed. A familiarization session will then be conducted on a separate day where all participants will practice the strength assessment, eccentric isokinetic protocol, and ultrasound assessments. Participants will be assigned to 1 of the 4 treatment groups based on their initial maximal isometric strength values using a matched-participants design. The first experimental session will then begin 2-10 days later, where the participants will perform the repeated eccentric exercise protocol (10 sets of 15 eccentric contractions 210 deg/sec with 3 min of rest between sets) with the non-dominant leg following a 60 min rest period where they will wear the apparel and perform a 5 min warm-up on a cycle ergometer. Follow-up blood draws and strength and ultrasound assessments will be obtained at 24 and 48 hours post-exercise. Each participant will also complete a visual analog scale at baseline, 24, 48, and 72 hours post-exercise to examine perceived muscle soreness.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Prevention
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Cohort of Adult Males & Females
  • Participant is between the ages of 18-35
  • Healthy, Recreationally Active (1-5 hours per week)
  • Participant has provided written and dated informed consent to participate in the study
  • Participant is apparently healthy and free from disease, as determined by a health history questionnaire
  • Participant agrees to abstain from smoking, caffeine (4hrs prior), tobacco (24hrs prior), and alcohol (24 hrs) before testing days
  • Participant agrees to abstain from exercise 24 hours prior to each testing visit and after 72 hours of the induced exercise damage
  • Participant will refrain from the use of non-steroidal anti-inflammatory drugs (NSAIDs) and protein supplementation 24 hours before the exercise testing protocol, as well as for the 72 hour period following the exercise testing protocol.

排除标准

  • Participant is using, or has used one of the following dietary supplements within 12 weeks prior to enrollment: beta-alanine, creatine, taurine, or any supplemental antioxidants (Acai, pomegranate, beet juice).
  • Participant is in, or has participated in another clinical trial within 6 weeks prior to enrollment
  • Participant has a known allergy or sensitivity to test product (determined from health history questionnaire and consent form)

研究组 & 干预措施

Test garment + Test garment

Active Comparator

Far Infrared Fabric during exercise + Far Infrared Fabric at night

干预措施: Far Infrared Fabric (Other)

Compression + normal garment

Active Comparator

Far Infrared Fabric during exercise + Spandex at night

干预措施: Far Infrared Fabric (Other)

Compression + normal garment

Active Comparator

Far Infrared Fabric during exercise + Spandex at night

干预措施: Spandex (Other)

Normal Garment + Test garment at night

Active Comparator

Spandex during exercise + Far Infrared Fabric at night

干预措施: Far Infrared Fabric (Other)

Normal Garment + Test garment at night

Active Comparator

Spandex during exercise + Far Infrared Fabric at night

干预措施: Spandex (Other)

Normal Garment + normal garment

Sham Comparator

Spandex during exercise + Spandex at night

干预措施: Spandex (Other)

结局指标

主要结局

Maximal Voluntary Contraction (MVC)

时间窗: up to 72 hours

次要结局

  • Creatine Kinase(baseline, 24 hrs and 48 hrs post)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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