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Technology-based Fall Risk Assessments for Older Adults in Low-income Settings

University of Central Florida logo

University of Central Florida

Status

Completed

Conditions

Physical Inactivity
Fall
Sedentary Behavior

Study type

Observational

Funder types

Other
NIH

Identifiers

NCT06063187
STUDY00002473
R03AG069799 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this observational study is to examine the associations among fall risk appraisal, body composition, and physical activity in older adults in low-income settings.

The main questions it aims to answer are:

  • What is the feasibility of recruitment (e.g., how many older adults need to be screened to recruit the sample?), especially during the COVID-19 pandemic, and acceptability of technologies and procedures for use among older adults in low-income settings?
  • What are the the dynamic relationships between fall risk appraisal, body composition, physical activity, and behavioral changes related to fear of falling?

Participants will:

  • complete questionnaires about their characteristics, socio-demographic, medical history, cognition, depressive symptoms, anxiety, and fear of falling.
  • participate in static and dynamic balance tests, body composition measurement and handgrip strength test.
  • wear an accelerometer for physical activity assessment for 7 consecutive days.

Full description

The investigators will use a cross-sectional design to address aims. The investigators will administer the study instruments which consist of objective and subjective measures. Participants will complete questionnaires about their characteristics, socio-demographic, medical history, cognition, depressive symptoms, anxiety, and fear of falling.

Balance performance will be assessed by the BTrackS Balance System (BBS). This test consists of four, 20 seconds trials. For each trial, the participants will stand as still as possible on the BBP with hands on their hips, and eye closed. This test consists of four trials. This test will take about 5-10 minutes.

Body composition will be assessed using a bioelectrical impedance analysis (BIA): InBody S10. The BIA InBody S10 measures fat mass, muscle mass and body water levels. There are no risks, no dunking, no pinching, no discomfort associated with the use of bioelectrical impedance analysis. Test duration is 1-2 minutes.

Physical Activity (PA) will be measured by activity monitoring devices. All participants will wear the ActiGraph GT9X Link wireless activity monitor (ActiGraph LLC.), a tri-axial accelerometer, on the non-dominant wrist for 7 consecutive days.

Enrollment

124 patients

Sex

All

Ages

60+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • ≥ 60 years of age
  • no marked cognitive impairment [Memory Impairment Screen (MIS) score ≥5]
  • speak English or Spanish
  • live in Kinneret Sr. Apartments or in Orlando FL.

Exclusion criteria

  • a medical condition precluding balance test (e.g., unable to stand on the balance plate) and/or PA (e.g., shortness of breath; feeling pressure when performing PA)
  • currently receiving treatment from a rehabilitation facility
  • have a metal implant.

Trial design

Trial documents
2

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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