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Clinical Trials/NCT06356142
NCT06356142CompletedEarly Phase 1

The Effects of Palmar Cooling on Repeated Sprinting Ability

University of Mississippi Medical Center2 sites in 1 country15 target enrollmentStarted: June 28, 2024Last updated:
Conditions

Trial Snapshot

Phase
Early Phase 1
Status
Completed
Enrollment
15
Locations
2
Primary Endpoint
Participants Sprinting times

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 30 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

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

Outcomes

Primary Outcomes

Participants Sprinting times

Time Frame: 1 day

Secondary Outcomes

  • Participants Heart Rate Recovery(1 day)
  • Participants Rating of Perceived exertion(1 day)
  • Participants Reported Delayed Onset Muscle Soreness(2 days after the intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jacob B. Daniels DPT, EdD

Assistant Professor

University of Mississippi Medical Center

Study Sites (2)

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