Evaluation of a Prototype for an Innovative Room for the Elderly

NCT ID: NCT06098534

Last Updated: 2025-06-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-11-09

Study Completion Date

2026-02-09

Brief Summary

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The Groupement de Coopération Sanitaire des Hôpitaux Universitaires du Grand Ouest (GCS HUGO) (health cooperation group for university hospitals in the west of France), is proposing to improve the quality of geriatric care by modernizing hospital rooms. The GCS HUGO has embarked on a project to co-design a hospital room adapted for the elderly, called "Hospi'Senior", with the help of the "Dépendance et Grand âge" (Dependency and Old Age) steering committee, made up of experts from HUGO's establishments and experts from several companies.

Detailed Description

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The main objective is to evaluate the effect of hospitalization in a Hospi'Senior room on the length of stay of elderly people compared with hospitalization in a conventional room for a similar admission reason.

The secondary objectives are to evaluate the effect of hospitalization in a Hospi'Senior room for elderly people, compared with hospitalization in a conventional room for a similar admission reason, on :

2\) Changes in functional abilities during the hospital stay and in the 30 days following discharge from the short-stay geriatric unit 3) Occurrence of behavioral disorders 4) Occurrence of falls during the hospital stay and in the 30 days following discharge from the short-stay geriatric unit 5) Occurrence and/or worsening of stage bedsores ≥ 2 during the hospital stay as classified by the National Pressure Ulcer Advisory Panel (NPUAP) 6) Occurrence of early rehospitalization

Conditions

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Elderly Inpatients

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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"Hospi'Senior" group

Patients admitted to the Hospi'Senior room benefit from the innovative technologies available in this room. Patients benefit from standard care throughout their hospital stay.

Group Type EXPERIMENTAL

Hospi'Senior

Intervention Type BEHAVIORAL

The Hospi'Senior room is equipped with conventional furnishings (same bed and same armchair as a conventional room) to which have been added technological innovations and innovations in furnishings. Innovative technologies cover bed equipment, patient mobility (autonomous and assisted), lighting, communication and social space.

"Conventional room" group

Patients admitted to a conventional room receive the standard care throughout their hospital stay.

Group Type EXPERIMENTAL

Conventional room

Intervention Type BEHAVIORAL

The conventional room is a classic hospital room not equipped with the innovative technologies found in the Hospi'Senior room.

The room is equipped with a bed, bedside table, adjustable bed table with castors and an armchair.

Interventions

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Hospi'Senior

The Hospi'Senior room is equipped with conventional furnishings (same bed and same armchair as a conventional room) to which have been added technological innovations and innovations in furnishings. Innovative technologies cover bed equipment, patient mobility (autonomous and assisted), lighting, communication and social space.

Intervention Type BEHAVIORAL

Conventional room

The conventional room is a classic hospital room not equipped with the innovative technologies found in the Hospi'Senior room.

The room is equipped with a bed, bedside table, adjustable bed table with castors and an armchair.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Age ≥ 75 years
* Admission in a short-stay geriatric department following initial emergency care department or direct entry from home
* Hospitalization in single room: Hospi'Senior or conventional
* Affiliation to a social security scheme
* Informed consent to participate in the study from the patient or his/her representative (tutor/curator if applicable, or in order of priority a trusted person, the family or a person with whom the person concerned has a close and stable relationship)

Exclusion Criteria

* Contraindication to study participation at the discretion of the medical team
* Hospitalization for more than 3 days (\>3 days) in the short-stay geriatric unit
* Hospitalization in a double room
* Planned hospitalization
* Poor understanding of the French language
* Patient under safeguard of justice
Minimum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Angers

OTHER_GOV

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Angers University Hospital

Angers, , France

Site Status RECRUITING

Brest University Hospital

Brest, , France

Site Status RECRUITING

Nantes University Hospital

Nantes, , France

Site Status RECRUITING

Rennes University Hospital

Rennes, , France

Site Status RECRUITING

Tours University Hospital

Tours, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Olivier BRIERE, MD

Role: CONTACT

+33 2 41 35 47 25

Facility Contacts

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Cédric ANNWEILER, MD, PhD

Role: primary

Armelle GENTRIC, MD, PhD

Role: primary

Guillaume CHAPELET, MD

Role: primary

Aline CORVOL, MD

Role: primary

Wassim GANA, MD

Role: primary

Other Identifiers

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49RC23_0276

Identifier Type: -

Identifier Source: org_study_id

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