MedPath

Technology and Human Help at Home After Hospitalisation

Not Applicable
Completed
Conditions
Patient Fall
Interventions
Behavioral: Interventional arm
Registration Number
NCT02335177
Lead Sponsor
Ages et Vies Association
Brief Summary

Elderly people are still at risk for falling at home. The objective of the study is to evaluate at home the impact of an intervention for 3 months combining technologies for autonomy and tailored physical activity program. The study is performed among patients aged 75 years and over leaving Charles Foix Geriatrics hospital or already supported by carer of professional home-care service Ages \& Vie and with a loss of autonomy requiring physiotherapy and home support workers. It is a prospective, randomized, single-center, in cluster study which compares a Patient group (interventional group) with the intervention program (technologies + physical activities) with a control group benefiting from usual care home. Our hypothesis is that in the interventional group fewer falls were observed and improved different scores (Timed Up and Go Test,Barthel index, Quality of Life questionnaire of Duke) were reported compared to the control group.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria
  • patients hospitalized in Charles Foix Hospital (France) and returning home or already supported by carer of professional home-care service Ages & Vie
  • > 75 years old with loss of autonomy
  • at risk for falling
  • able to read and understand the information letter and consent letter
  • patient requiring physiotherapy and caregiver at home.
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Interventionnal armInterventional armInterventional arm : patients at home with technologies for autonomy and tailored physical activity program.
Primary Outcome Measures
NameTimeMethod
Number of falls3 months

absence of fall requiring medical or paramedical care and improvement of the Timed Up and Go Test (TUG) or improvement of the autonomy level assessed by Barthel Index with at least stability of the test that is not improved

Secondary Outcome Measures
NameTimeMethod
Duke questionnaire3 months
Timed up and Go test score3 months
Barthel index3 months

Trial Locations

Locations (1)

AP-HP Charles Foix

🇫🇷

Ivry sur Seine, France

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