Skip to main content
Clinical Trials/NCT05950269
NCT05950269
Completed
N/A

Walking Aid and Locomotion Knowledge in Emergency Rooms (WALKER 1): Training and Provision of Walking Aids to Promote Autonomy and Mobility of Elderly People in Emergency Care - a Randomized Clinical Trial

Hospital Sirio-Libanes1 site in 1 country153 target enrollmentJuly 31, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Mobility Limitation
Sponsor
Hospital Sirio-Libanes
Enrollment
153
Locations
1
Primary Endpoint
Life-Space Assessment (LSA)
Status
Completed
Last Updated
last year

Overview

Brief Summary

Older adults have higher rates of emergency department admissions when compared to their younger counterparts. Mobility is the ability to move around but also encompasses the environment and the ability to adapt to it. Walking aids can be used to improve mobility and prevent falls. According to international guidelines, they must be available in Geriatric Emergency Department. This study aims to evaluate the effectiveness of a program of training and provision of walking aids (WA), associated or not with telemonitoring, on mobility, quality of life, fear of falling, and risk of falls up to 3 months in older adults cared for in an emergency department.

Detailed Description

A randomized clinical trial will be carried out in the emergency department of Hospital Sírio-Libanês. Participants will be randomized and allocated into three intervention groups, as follows: A) Walking aid group; B) Walking aid and telemonitoring group; C) Control group. Patients will undergo a baseline evaluation encompassing sociodemographic and clinical data, mobility in life spaces (Life Space Assessment), gait speed, muscle strength, functionality (Barthel Index, Katz index, and Lawton-Brody Scale), quality of life (Euro Quality of Life Instrument-5D), fear of falling (Falls Efficacy Scale International), history of falls, cognition (10-Point Cognitive Screener) and mood (15-point Geriatric Depression Scale) before the intervention. Gait time and fear of falling will be assessed again after the intervention. Finally, mobility in life spaces, functionality, quality of life, fear of falling, history of falls, cognition, and mood will be assessed 3 months after discharge from the geriatric emergency department through a telephone interview.

Registry
clinicaltrials.gov
Start Date
July 31, 2023
End Date
December 28, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hospital Sirio-Libanes
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 65 years or older
  • Admitted to the Geriatric Emergency Department of Hospital Sírio-Libanês
  • Willing and able to give informed consent
  • Least one of the following for indication and training of mobility aids: reduction of postural instability; improvement of motor control; increase of somatosensory feedback; reduction of biomechanical overload; safe promotion of autonomy; fall history (in the last six months).

Exclusion Criteria

  • Altered level of conscience
  • need for supplemental oxygen (≥3L/min)
  • respiratory distress
  • hemodynamic instability
  • postural instability with a tendency to fall backward
  • cognitive impairment that limits the use of walking aids
  • hospitalization after Emergency Department evaluation

Outcomes

Primary Outcomes

Life-Space Assessment (LSA)

Time Frame: At baseline and after completion of the 3 and 6 months intervention to assess change

LSA is a scale which allows the characterization of mobility in life-spaces specifically frequency, need for mobility aids and the help of third party in the last 4 weeks

Falls Efficacy Scale International (FES-I)

Time Frame: At baseline, immediately after the intervention and after completion of the 3 and 6 months intervention to assess change

Assesses fear of falling

Secondary Outcomes

  • Geriatric Depression Scale (GDS-15)(At baseline and after completion of the 3 and 6 months intervention to assess change)
  • 10-Point Cognitive Screener (10-CS)(At baseline and after completion of the 3 and 6 months intervention to assess change)
  • Fall History(At baseline and after completion of the 3 and 6 months intervention to assess change)
  • Timed Up and Go test (TUG)(At baseline and immediately after the intervention)
  • Katz index(At baseline and after completion of the 3 and 6 months intervention to assess change)
  • Lawton-Brody scale(At baseline and after completion of the 3 and 6 months intervention to assess change)
  • Euro Quality of Life Instrument-5D (EQ-5D)(At baseline and after completion of the 3 and 6 months intervention to assess change)
  • One-minute sit-to-stand test(At baseline and after completion of the 3 and 6 months intervention to assess change)
  • Barthel index(At baseline and after completion of the 3 and 6 months intervention to assess change)

Study Sites (1)

Loading locations...

Similar Trials