RECRUITING

FIT Exercise in 30d of ULLS-induced Muscle Disuse

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Conditions

Muscle AtrophyMuscle Weaknessspaceflightunweightingdisuseexercise

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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

This study aims to determine how flywheel-based inertial training (FIT) implemented according to principles of velocity-based training (VBT) and High-Intensity Interval Training (HIIT) affects disuse-induced physical de-conditioning including loss of voluntary muscle strength, aerobic capacity, and balance regulation.

Official Title

Use of Velocity Monitoring to Prescribe Appropriate Flywheel-based Inertial Training (FIT) Workloads for Exercise in Space Flight

Quick Facts

Study Start:2024-10-23
Study Completion:2025-09-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06631053

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:35 Years to 45 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Regularly engaging in aerobic exercise (\> 150min/wk) and resistance exercise (\>1 time per week) for the past 12 months
  2. * Education greater than or equal to bachelor's degree (any field)
  1. * Waist circumference \< 55cm or \> 90cm (F) and \< 75cm or \> 100cm (M)
  2. * Body mass index \< 18.5 or \> 29.9
  3. * Shoe size \< 25 or \>29cm.
  4. * Not regularly engaging in exercise for previous 12 months
  5. * Tobacco use within previous 6 months
  6. * Blood clotting disorder
  7. * Heart arrhythmia
  8. * Implanted device which could negatively be affected by electrical impulse or strong magnetic field such as pacemaker, internal defibrillator, or cochlear implant
  9. * Diagnosed cardiovascular, pulmonary, renal, or metabolic disease
  10. * Pregnancy (within previous 6 months)
  11. * Oral contraceptive use (within previous three months)
  12. * High resting blood pressure (\>140 systolic and/or \> 90 diastolic)
  13. * Currently or previously undergone gender-affirming therapy (hormone therapy or sexual reassignment surgery)
  14. * Low back or leg injury in previous 6 months
  15. * Currently taking medication to assist with sleep
  16. * Muscle, bone, or joint injury that limits physical activity within previous 6 months
  17. * Neurological disorder which affects balance (such as multiple sclerosis or Parkinson's disease)

Contacts and Locations

Study Contact

Lance Bollinger, PhD
CONTACT
8592577904
lance.bollinger@uky.edu

Principal Investigator

Lance Bollinger, PhD
PRINCIPAL_INVESTIGATOR
University of Kentucky

Study Locations (Sites)

University of Kentucky
Lexington, Kentucky, 40506
United States

Collaborators and Investigators

Sponsor: Lance Bollinger

  • Lance Bollinger, PhD, PRINCIPAL_INVESTIGATOR, University of Kentucky

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 Date2024-10-23
Study Completion Date2025-09-01

Study Record Updates

Study Start Date2024-10-23
Study Completion Date2025-09-01

Terms related to this study

Keywords Provided by Researchers

  • spaceflight
  • unweighting
  • disuse
  • exercise

Additional Relevant MeSH Terms

  • Muscle Atrophy
  • Muscle Weakness