RECRUITING

The Effects of High-Intensity Functional Training in Tactical Populations

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Healthyhigh-intensity functional trainingtacticalmilitary

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to investigate the effects of high-intensity functional training (HIFT) as compared to traditional resistance training (RT) and concurrent training consisting of RT and high-intensity interval training (HIIT) on physical performance metrics, body composition, and mental and physical readiness of tactical personnel.

Official Title

The Effects of High-Intensity Functional Training Versus Traditional Strength Training or Concurrent Training on Performance and Readiness in Tactical Populations

Quick Facts

Study Start:2024-08-26
Study Completion:2026-01-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06582251

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 35 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Males and females between the ages of 18 and 35 (inclusive) and enrolled in a reserve officer training corps program.
  2. * Subject has provided written and dated informed consent to participate in the study.
  3. * Subject is in good health as determined by medical history and is cleared for exercise.
  4. * BMI between 17.0 and 29.9 kg/m2.
  5. * "Good" category or greater for their aerobic capacity according to the American College of Sports Medicine (ACSM) normative data for their age and sex as measured at their baseline visit.
  1. * Participants with any musculoskeletal injuries that would prevent completion of these exercise programs.
  2. * Participants with any metabolic disorder, including known electrolyte abnormalities, uncontrolled diabetes, uncontrolled thyroid disease, adrenal disease, or hypogonadism.
  3. * Participants with a history of hepatorenal, musculoskeletal, autoimmune, or neurologic disease.
  4. * Participants who have lost or gained greater than eight pounds within three months prior to study enrollment.
  5. * Participants currently taking hyperlipidemic, hypoglycemic, anti-hypertensive, or anti-coagulant medications.
  6. * Participants who are pregnant or lactating.

Contacts and Locations

Study Contact

Shawn M Arent, PhD
CONTACT
8035768394
sarent@mailbox.sc.edu
Gianna F Mastrofini, MS
CONTACT
7034246509
giannafm@email.sc.edu

Study Locations (Sites)

University of South Carolina Sport Science Lab
Columbia, South Carolina, 29208
United States

Collaborators and Investigators

Sponsor: University of South Carolina

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-08-26
Study Completion Date2026-01-01

Study Record Updates

Study Start Date2024-08-26
Study Completion Date2026-01-01

Terms related to this study

Keywords Provided by Researchers

  • high-intensity functional training
  • tactical
  • military

Additional Relevant MeSH Terms

  • Healthy