RECRUITING

High Intensity Interval Training (HIIT) to Reduce Frailty and Enhance Resilience in Older Veterans

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

Frailty is defined as a greater susceptibility to stressors resulting from age-related impairments in adaptive biological systems. Frailty leads to poorer physical performance and functional capacity and higher risk of adverse outcomes including falls, hospitalization, and mortality. Resilience, defined as the capacity to recover from disruptions to homeostasis, is critical to successful aging because it precedes frailty and enhances adults' ability to maintain optimal health and function well into older age. Evidence- based therapies to help older adults enhance resilience are limited and the biological underpinnings contributing to improved resilience have not yet been fully characterized. To address this important need, the investigators will conduct a clinical trial to examine the benefits of center- and home-based high intensity interval training (HIIT) on functional capacity, frailty, and resilience, and also to identify novel biomarkers of resilience in older Veterans.

Official Title

High Intensity Interval Training (HIIT) to Reduce Frailty and Enhance Resilience in Older Veterans

Quick Facts

Study Start:2024-01-29
Study Completion:2027-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05625204

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:60 Years to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Ages 60 years
  2. * Male and female, any race
  3. * Medically cleared for exercise
  4. * Non-frail or pre-frail (frailty score \< 3)
  1. * Severe co-morbidity: COPD (GOLD stage IV), CKD ( stage 3)), severe HTN (180 mmHg/120 mmHg)
  2. * VA-SLUMS score 20 (Cognition)

Contacts and Locations

Study Contact

Kenneth L Seldeen, PhD
CONTACT
(716) 888-4869
Kenneth.Seldeen@va.gov
Bruce R Troen, MD
CONTACT
(816) 922-2755
Bruce.Troen@va.gov

Principal Investigator

Bruce R. Troen, MD
PRINCIPAL_INVESTIGATOR
Kansas City VA Medical Center, Kansas City, MO

Study Locations (Sites)

Kansas City VA Medical Center, Kansas City, MO
Kansas City, Missouri, 64128-2226
United States
Kansas City VA Medical Center, Kansas City, MO
Kansas City, Missouri, 64128
United States

Collaborators and Investigators

Sponsor: VA Office of Research and Development

  • Bruce R. Troen, MD, PRINCIPAL_INVESTIGATOR, Kansas City VA Medical Center, Kansas City, MO

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 Date2024-01-29
Study Completion Date2027-12-31

Study Record Updates

Study Start Date2024-01-29
Study Completion Date2027-12-31

Terms related to this study

Keywords Provided by Researchers

  • aging
  • frailty
  • veteran
  • functional capacity
  • resilience
  • cognition
  • sleep

Additional Relevant MeSH Terms

  • Frailty