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OpenTrials
Completed

NCT Number: NCT06356142

The Effects of Palmar Cooling on Repeated Sprinting Ability

Repeated sprinting ability is key for athletic performance in a variety of sport settings. Significant degradations in work output (i.e. fatigue) have been shown to develop after just one sprinting bout1. This pilot study aims to investigate the effects that noninvasive transient temperature manipulation has on an individual's ability to perform repeated sprints. The investigators aim to enroll 90 healthy individuals, 18-30 years of age. Participants will be randomized into two groups (Group A, and B). All groups will perform a ten-minute warm-up followed by two minutes of rest. Following the warm-up and rest period, all groups will participate in a series of five sprints, 60 meters in total length with two 180 degree changes in direction. Between sprints, participants will have 10 seconds rest. After the first series of five sprints participants will be given a 2-minute rest interval. Then participants will perform another series of five sprints followed by another 2-minute rest interval. During each rest interval, Group A will utilize a palmar cooling device. Group B will utilize a placebo version of the palmar cooling device. All sprints will be timed. Heart rate recovery will be measured during all rest breaks, and a rating of perceived exertion will be measured at the beginning and end of each resting interval. Delayed onset muscle soreness will be assessed 48 hours post sprinting, utilizing a visual analog scale.

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Key information

Age range

18 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

University of Mississippi Medical Center

Jackson, Mississippi, 39216, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy individuals 18-30 years of age

Exclusion criteria

  • Participant self-reporting injury or illness that will prevent them from exercising at maximal capacity
  • If participant has been told by their healthcare provider that they should avoid exercising at maximal capacity
  • Has previously used the palmar cooling device

Treatment and study plan

Palmar Cooling

Device

Palmar cooling device will be utilized for 2 minutes during rest breaks.

Placebo Palmar Cooling

Device

Placebo Palmar cooling device will be utilized for 2 minutes during rest breaks

Primary outcomes

  1. Participants Sprinting times

    Time frame: 1 day

Secondary outcomes

  1. Participants Heart Rate Recovery

    Time frame: 1 day

  2. Participants Rating of Perceived exertion

    Time frame: 1 day

    Borg RPE Scale (6-20)

  3. Participants Reported Delayed Onset Muscle Soreness

    Time frame: 2 days after the intervention

    Visual Analog Scale 1-10

Sponsors and collaborators

Lead sponsor

University of Mississippi Medical Center

Other

Registry information

Important dates

Study start
2024
Primary completion
2024
Study completion
2024
First posted
Apr 10, 2024
Registry last updated
Jun 6, 2025

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.