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Measuring the Impact of Taking Care in the Context of an Innovative System for Keeping Dependent Elderly People in Their Homes (DIAPASON)

G

Gérond'if

Status

Enrolling

Conditions

Patient With no Severe Behavioural Disorders and Whose Situation Would Require Entry Into Classique EHPAD (Retirement Home)

Study type

Observational

Funder types

Other

Identifiers

NCT03976661
2018-A03183-52

Details and patient eligibility

About

The purpose of this study is to compare life quality of patients taking care by DIAPASON 92 with patients or residents from control group EHPAD (retirement home)

Full description

This study has two components: a quantitative component(for users and caregivers) and a qualitative component (for users, caregivers and professionals)

About population :

For quantitative component: the investigators have two arms:

  • Diapason 92 arm: will be constitued by older patients with loss of autonomy, living at home and benefiting from Diapason 92 device
  • Control arm: will be constituted by people residing at the EHPAD (retirement home)

For qualitative component: Study will cover 5 different populations since it concerns both:- - Diapason 92 professionals who work directly with users

  • Daipason 92 Supervisory staff
  • Diapason 92 professional partners, including referring physicians.
  • The users
  • Non-professional helpers of users

Conduct of study:

  • About quantitative component:

After verification of eligibility criteria adapted to each centre and once the non-opposition has been collected and subjects have been included, the following data will be collected at M0, M3, M6 and M12:

  • For patients : Start date of care by Diapason 92 or EHPAD, Quality of Life score, benefit evaluation, Socio-educational level, evaluation of disruptive behaviour disorders, economic indicators, somatic comorbidities, collection of psychiatric follow-up if available, independence, nutritional status, factors(s) that motivated care, cognitive assessment, balance assessment, depression screening, ergonomic assessment (only for Diapason 92
  • Family caregiver: 3 measures will be collected: Measuring the burden by Zarit scale, self-assessment of his quality of life and psychological condition
  • About quality component:

A socio-demographic heel will be collected for each participant interviewed who has given no objection to participating in the study. His agreement on the recording of his voice will also collected.

For all participants, following data will be collected: Age, sex, occupation, date and duration of the interview, relationship with the Diapason 92 user (for family caregivers) and the recovery of socio-demographic data of the case report form (for users)

Enrollment

86 estimated patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Patient/Resident Inclusion Criteria

  • Age ≥ 60 years old.
  • (Group iso-resources) GIR ≤ 4
  • Beneficiary of treatment by Diapason 92 or resident at EHPAD Aulagnier for more than 6 months.
  • Not exhibiting severe disruptive behaviour disorders (on NPI-ES all FXG 12 and resonance 4 scores).
  • Affiliate or entitled to a sickness insurance scheme
  • Patient or legal representative expressed no objection

Patient/Resident Exclusion Criteria:

  • Age < 60 years old
  • GIR ˃ 4
  • Not affiliated or entitled to a sickness insurance scheme
  • Patient or legal representative did not express no objection

Professionals and caregivers Inclusion Criteria:

  • Exercise within Diapason 92 device or be identified as assisting a Diapason 92 user or be a professional partner of Diapason 92 device
  • Have expressed no objection to participating in the study.

Trial design

86 participants in 2 patient groups

DIAPASON 92 arm
Description:
Arm will be constitued by older patients with loss of autonomy, living at home benefiting from the device DIAPASON 92 (Innovative support system for elderly people in their homes)
Control arm
Description:
Arm will be constituted by people residing at the EHPAD (retirement home)

Trial contacts and locations

1

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Central trial contact

Prisca Lucas, PhD; Isabelle Dufour

Data sourced from clinicaltrials.gov

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