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OpenTrials
Completed

NCT Number: NCT02076334

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

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.

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Key information

Conditions

Age range

18 year–35 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Exercise and Sport Science (University of North Carolina)

Chapel Hill, North Carolina, 27599, United States

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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)

Treatment and study plan

Far Infrared Fabric

Other

Spandex

Other

Primary outcomes

  1. Maximal Voluntary Contraction (MVC)

    Time frame: up to 72 hours

Secondary outcomes

  1. Creatine Kinase

    Time frame: baseline, 24 hrs and 48 hrs post

Sponsors and collaborators

Lead sponsor

University of North Carolina, Chapel Hill

Other

Collaborators

  • Rhodia, Inc

Registry information

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Mar 3, 2014
Registry last updated
Jul 11, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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