Assessing a New Tool to Assess Frailty in Frail Hospitalized Elderly

Overview

The major purpose of this study is to establish the use of daily step counts as inexpensive, easy to measure marker for frailty and sarcopenia in an inpatient population of older adults.

Study Type

  • Study Type: Observational
  • Study Design
    • Time Perspective: Prospective
  • Study Primary Completion Date: December 2023

Detailed Description

The total time involved to complete study procedures will be between 2-3 hours at your enrollment and up to 10 minutes at your discharge. Investigators will invite participants to enrol in this study at your admission and discharge days. Firstly, Investigators would like to collect some demographic data, including participants age and gender. Then Investigators will ask participants to check their blood pressure and heart rate, weight, height and Body Mass Index. Also Investigators will collect participant's medication List and Past Medical History. Then, Investigators would like to ask participants to carry special device on their mid-thigh. It's called 'ActivPAL' and a trained research assistant will fit it on participant's dominant leg. This device has ability to detect the joint angle of participant's thigh to capture lying, sitting, standing, and stepping activities. Then Investigators will proceed to ultrasound test. Participants will be asked to lay down on the bed with their legs supported by a pillow. Then a study physician will use ultrasound to measure participant's leg muscles. Three measurements will be taken for each participant. After that participant will be asked to do a "Grip test". Participant will be asked to squeeze special device, called dynamometer, using your dominant hand. Each participant will be asked to make three attempts with half a minute break between each measurement. Participant will be asked to walk 10-15 meters in order to measure their gait speed. Impedance measures of body composition will be performed using an automatic scale. At the end Investigators will ask you to measure participant's body structure, using skinfold/caliper device. At participant discharge Investigators will remove 'ActivPal' sensor from their leg that was fitted at enrollment.

Interventions

  • Device: ActivPAL3 VT (PAL Technologies Ltd).
    • . The ActivPAL will be fitted by a trained research assistant on the mid-thigh of the participants’ dominant leg. ActivPALs have an inclinometer that detects the joint angle of the thigh to capture lying, sitting, standing, and stepping activities.

Arms, Groups and Cohorts

  • Frail hospitalized old adults
    • Over than 65-years of age Admitted into Acute Unit Nonambulatory

Clinical Trial Outcome Measures

Primary Measures

  • Total standing time
    • Time Frame: 2 weeks or shorter
    • Total upright time will show a strong association with both continuous measures of frailty (Clinical Frailty Scale) and the presence of sarcopenia, as measured by ultrasound and bioelectric impedance measures.

Secondary Measures

  • Daily step counts
    • Time Frame: 2 weeks or shorter
    • 2. Daily step counts will show strong correlations with patient outcomes (length of stay, readmission rates, discharge to care facility, functional outcomes at 1year, and mortality rates).

Participating in This Clinical Trial

Inclusion Criteria

  • be 65 years of age or older – be admitted in ACE Unit Exclusion Criteria:

  • be less than 65 years of age – be nonambulatory – be diagnosed with end-stage organ failure (end-stage COPD, renal failure requiring dialysis, end-stage heart failure)

Gender Eligibility: All

Minimum Age: 65 Years

Maximum Age: N/A

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • University of British Columbia
  • Provider of Information About this Clinical Study
    • Principal Investigator: Kenneth Madden, Principal Investigator – University of British Columbia
  • Overall Official(s)
    • Kenneth Madden, MD, Principal Investigator, UBC

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