Cardiac Rehabilitation Mobile-Health Fall Risk Prevention Intervention

Part of paid clinical trials in Scottsdale, Arizona.

Sponsor
Mayo Clinic
Study ID
NCT05826587
Status
Recruiting

Conditions

  • Cardiac Rehabilitation

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Home-based, m-Health Delivered Physical Function Training — BEHAVIORAL
    An individualized home exercise physical function training will be prescribed. This would include 5 balance training exercises and 1-2 upper and lower-body muscular conditioning exercises (i.e., wall push-up and chair stand) prescribed 3 days/week over the course of a 6-week period. Subjects will be assigned exercises from 1 of 3 different levels of exercise progression based on performance during the baseline muscular fitness assessment (functional chair stand and static chest throw).
  • Cardiac Rehabilitation & Exercise Prescription — BEHAVIORAL
    Standard, clinically indicated cardiac rehabilitation and exercise program. Approximately 30 to 40 minutes of aerobic exercise within a prescribed rating of perceived exertion (RPE 11-14) and/or target heart rate and approximately 15 to 20 minutes of both upper and lower body resistance exercise up to three times per week for up to at least 12 weeks. In addition, subjects are provided with home exercise instructions, and will be expected to exercise for 30 to 60 minutes at home.
  • Connected mHealth mobile application — OTHER
    Mobile application that allows subjects to track their independent home exercise with the option of heart rate monitoring by connecting to an external heart rate monitoring device.

Study Details

The purpose of this research is to see if taking part in a structured exercise plan that is designed to improve balance and muscle strength and one that can done at home helps to improve the ability to perform standard physical tasks, confidence in balance, and health-related quality-of-life

Key Dates

Start date
Oct 9, 2023
Status verified
Jan 2026
Primary completion
Jan 5, 2026
Completion
Dec 31, 2026

Study Design

Enrollment
128 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE

Arms

  • Active Comparator: Control group of cardiac rehabilitation only
  • Experimental: Intervention group of additional balance and muscle strength training

Primary Outcome Measure

Change in self-reported physical function [ Time Frame: Baseline, approximately 7 to 14 weeks ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Mayo Clinic ArizonaScottsdaleArizona85259
Robert Scales
4807918935
Mayo Clinic FloridaJacksonvilleFlorida32224
Kevin Kurtz
9049538436
Bryan Taylor, PhD (PRINCIPAL_INVESTIGATOR)

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