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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03976661
Other study ID # 2018-A03183-52
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 29, 2019
Est. completion date April 26, 2024

Study information

Verified date January 2023
Source Gérond'if
Contact Isabelle Dufour
Phone +33 (0) 185781010
Email isabelle.dufour@gerondif.org
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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)


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)


Recruitment information / eligibility

Status Recruiting
Enrollment 86
Est. completion date April 26, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms

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

Locations

Country Name City State
France Geriatric department , Broca Hospital Paris Ile-de-France

Sponsors (1)

Lead Sponsor Collaborator
Gérond'if

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of life quality according Nottingham Health Profile (NHP) scale Difference in 12-month quality of life scores (Nottingham Health Profile) between the 2 groups (Diapason 92 and EHPAD). 12 months
Secondary Assessment of the level of loss of autonomy of an elderly people according Autonomy, gerontology Iso Resources Group (AGGIR) scale 12 months
Secondary Assessment of functional status according Lawton Instrumental Activities of Daily Living (IADL) Scale 12 months
Secondary Assessment of activities of daily living, self-care, and independence according Activities of Daily Living (ADL) Scale 12 months
Secondary Assessment of comorbidity according Charlson scale 12 months
Secondary Assessment of cognitive function according Mini-Mental State Examination (MMSE) scale 12 months
Secondary Assessment of disorders of disruptive behaviour according (NPI-ES) scale 12 months
Secondary Assessment of geriatric depression according Geriatric Depression Scale (GDS) scale 12 months
Secondary Measuring of burden of the close caregivers according Popular Caregiver Self-report measure Burden (ZARIT) 12 months