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The Effects of Palmar Cooling on Repeated Sprinting Ability

University of Mississippi logo

University of Mississippi

Status and phase

Completed
Early Phase 1

Conditions

Exercise Induced Fatigue

Treatments

Device: Placebo Palmar Cooling
Device: Palmar Cooling

Study type

Interventional

Funder types

Other

Identifiers

NCT06356142
UMMC-IRB-2023-317

Details and patient eligibility

About

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.

Enrollment

15 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

15 participants in 2 patient groups, including a placebo group

Intervention Group
Experimental group
Treatment:
Device: Palmar Cooling
Control
Placebo Comparator group
Treatment:
Device: Placebo Palmar Cooling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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