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Clinical and Medico-economic Evaluation of the Cohort "People at Risk of Falling" (PARC)

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status

Completed

Conditions

Fall Patients

Treatments

Other: Innovativ supported

Study type

Interventional

Funder types

Other

Identifiers

NCT03545529
38RC16.044

Details and patient eligibility

About

The goal of this study is to evaluate the effectiveness of the IsereADOM service package compared to conventional follow-up on the risk of recurrence of falls at 6 months in frail elderly subjects.

There is a medico-economic goal too, is to conduct a cost-utility analysis of the IsereADOM service bundle compared to conventional 6-month follow-up from the community perspective in the cheat population at risk of re-offending.

Enrollment

14 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria :

  • Patient falling at least 2 times in the year preceding the inclusion, one of them has been reported or consulted by a health care service ;
  • Patient fragile and loss of autonomy: level of dependence with GIR 3, 4 and 5 ;
  • Patient domiciled in the department of Isère ;
  • Patient who can be followed regularly for 6 months ;
  • Patient benefiting from an assistance plan : APA, PAP, CARSAT ;
  • Patient affiliated with social security or beneficiary of such a scheme ;
  • Patient able to read, write and understand French ;
  • Patient having signed informed consent to participate.

Exclusion Criteria :

  • Patient without professional or family carer of proximity ;
  • Patient with moderate to severe cognitive impairment defined by MMS <23 ;
  • Patient residing in a nursing home or institution for dependent person ;
  • Persons referred to in Articles L1121-5 to L1121-8 of the CSP (corresponds to all persons protected: pregnant woman, parturient, mother who is breastfeeding, person deprived of liberty by judicial or administrative decision, person subject of a legal protection measure).

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

14 participants in 2 patient groups

Innovative supported
Experimental group
Description:
In addition to usual care, patients benefit from connected tools (telealarm, numeric communication diary...) and from a strong accompaniment with a referent person who help better the patient.
Treatment:
Other: Innovativ supported
conventional supported
No Intervention group
Description:
Patients benefit from usual care

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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