RECRUITING

Using Consumer-grade Wearable Devices for Fall Risk Evaluation and Alerts

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

Creation and use of a smartphone application for older adults to assess the participants' risk of fall. Phase 1: Compare the accuracy and validity of accelerometer and gyroscopic data from a smartphone and gold-standard, wearable sensors gathered during balance and gait activities. Phase 2: Develop a model that integrates wearable sensor data and individual characteristics, such as age, medical conditions, exercises, previous falls, fear of falls, along with gait and balance outcome measurements, to evaluate fall risk in older adults. Phase 3: Integrate the computational model in the design of a mobile app for wearable devices for older adults to self-administer fall risk assessments and provide individualized risk of fall information.

Official Title

Using Consumer-grade Wearable Devices for Fall Risk Evaluation and Alerts

Quick Facts

Study Start:2024-07-29
Study Completion:2026-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06508892

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:65 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * 65 years or older
  1. * have had a fall in the six months
  2. * have been diagnosed with neurological conditions such as multiple sclerosis, Parkinson's disease, traumatic brain injury, Alzheimer's disease, or have had a stroke in the last year
  3. * have orthopedic or cardiopulmonary conditions and/or surgeries in the past year
  4. * have physical limitations that would make it difficult or uncomfortable for individuals to perform the experimental tasks.

Contacts and Locations

Study Contact

Nathan Miller, Ph.D.
CONTACT
810-762-3234
natmille@umich.edu
Cathy A Larson, PT, Ph.D.
CONTACT
8107623373
clarson@umich.edu

Principal Investigator

Jennifer Liao, PT, Ph.D.
PRINCIPAL_INVESTIGATOR
University of Michigan-Flint

Study Locations (Sites)

University of Michigan-Flint
Flint, Michigan, 48502
United States

Collaborators and Investigators

Sponsor: University of Michigan

  • Jennifer Liao, PT, Ph.D., PRINCIPAL_INVESTIGATOR, University of Michigan-Flint

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 Date2024-07-29
Study Completion Date2026-12-31

Study Record Updates

Study Start Date2024-07-29
Study Completion Date2026-12-31

Terms related to this study

Keywords Provided by Researchers

  • fall risk

Additional Relevant MeSH Terms

  • Mass Screening