RECRUITING

Exercise From Afar: Progressing At Risk Individuals to Independent Exercise

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 efficacy of a technology-driven independent exercise program on health outcomes associated with dementia risk among underactive rural adults. Underactive adults (n=50), ages 40-70 years, from federally designated rural and frontier Kansas counties will be recruited to participate in this study. Specific inclusionary and exclusionary criteria will be used to screen potential participants and determine eligibility. Following recruitment and screening, participants will complete baseline physical fitness and health assessments, supervised by the research team. Following completion of baseline assessments, a personal training/fitness app will be employed to design and deliver exercise programming and track exercise participation, adherence and progression over the course of the study. All prescribed exercise will follow national governing body recommendations and include specific exercises found in previous work to be beneficial for physical health and brain plasticity. The study team will record exercise instruction videos that can be accessed by all participants at any time throughout the study. The particular app used will allow the research team to organize exercise videos into structured training sessions, allowing participants to exercise on their own, at the location of their choice, with ample instruction. The app will also allow participants to record themselves performing various exercises and send them to the research team for analysis of technique and safety. Communication between study personnel and participants will be delivered via the app. Phone calls and/or Zoom sessions will be offered as an alternative if necessary. Our goal is to create a safe, effective means of delivering personalized exercise programming to rural adults that reduces barriers to exercise, improves physical fitness and biomarkers associated with dementia risk and lends itself to exercise adherence in a population that is at an increased risk for cognitive decline. Middle aged adults will be included in the study as they are at an age when successful behavior change is more probable (than older, institutionalized adults); older adults will be included as they are in the high-risk category for dementia. Following the exercise intervention, all baseline assessments will be repeated. Data will be compared to determine the impact of the exercise program on each variable (i.e. dementia risk biomarkers, QOL, physical fitness, etc.).

Official Title

Exercise From Afar: Progressing At-Risk Rural Adults to Effective Independent Exercise for Dementia Risk Reduction

Quick Facts

Study Start:2024-11-01
Study Completion:2025-05-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06667817

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:40 Years to 70 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 40 to 70 years of age
  2. * Characterized as underactive by the TAPA
  3. * Able to read and converse in English
  4. * Willing and able to install an application on their smart phone
  1. * Myocardial infarction or symptoms of coronary artery disease in the last 2yrs
  2. * Uncontrolled hypertension within the last 6 months
  3. * Cancer in the last 2yrs (except non-metastatic basal or squamous cell carcinoma)
  4. * Significant pain or musculoskeletal disorder that would prohibit participation in an exercise program
  5. * Possible/probably dementia or mild cognitive impairment (MCI) base on adjudication
  6. * Physician concern regarding safety or completion of the study

Contacts and Locations

Study Contact

Erin M Blocker, PhD
CONTACT
620-803-6161
eblocker@emporia.edu
Bryan Jones
CONTACT
620-341-5351
bjones17@emporia.edu

Principal Investigator

Erin M Blocker, PhD
PRINCIPAL_INVESTIGATOR
Emporia State University

Study Locations (Sites)

Emporia State University
Emporia, Kansas, 66801
United States

Collaborators and Investigators

Sponsor: Emporia State University

  • Erin M Blocker, PhD, PRINCIPAL_INVESTIGATOR, Emporia State University

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 Date2024-11-01
Study Completion Date2025-05-01

Study Record Updates

Study Start Date2024-11-01
Study Completion Date2025-05-01

Terms related to this study

Additional Relevant MeSH Terms

  • Sedentary Behavior