Connecting Emergency Departments With Community Services to Prevent Mobility Losses in Pre-frail & Frail Seniors

NCT03991598 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1500

Last updated 2019-06-19

No results posted yet for this study

Summary

About 18% of independent people over 65 who are evaluated in Emergency Departments for minor injuries (fractures, sprains) present some mobility decline up to 3 to 6 months postinjury. People at risk of decline are prefrail or frail; this condition could be explained by muscle proprieties loss. Exercise is a proven method that can help limit frailty and allow to restore mobility.

The aim of our study is to evaluate whether a suitable exercise program of one hour, twice a week for 12 weeks will limit functional losses \& fragility in injured older adults after their emergency department visit.

Conditions

  • Elderly
  • Functional Status

Interventions

OTHER

Exercise program

Exercise program in communities / Exercise program at home

Sponsors & Collaborators

  • Université du Québec a Montréal

    collaborator OTHER
  • University of Toronto

    collaborator OTHER
  • Laval University

    collaborator OTHER
  • Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal

    collaborator OTHER
  • Ottawa Hospital Research Institute

    collaborator OTHER
  • Centre de recherche du Centre hospitalier universitaire de Sherbrooke

    collaborator OTHER
  • Alberta Health Services, Calgary

    collaborator OTHER
  • Sunnybrook Research Institute

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • McMaster University

    collaborator OTHER
  • Mount Sinai Hospital, Canada

    collaborator OTHER
  • The Ottawa Hospital

    collaborator OTHER
  • Université de Montréal

    collaborator OTHER
  • University of Ottawa

    collaborator OTHER
  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • CHU de Quebec-Universite Laval

    lead OTHER

Principal Investigators

  • Marcel ME Emond, Md, Ph.D · Centre de recherche du CHU de Québec

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
65 Years
Max Age
120 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-07-01
Primary Completion
2020-06-30
Completion
2020-07-31

Countries

  • Canada

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03991598 on ClinicalTrials.gov