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User ExperienceHospiSenior-UXNCT05126212

Evaluation of the User Experience of an Innovative Hospital Room Prototype Adapted to the Elderly

An observational study of User Experience, run by University Hospital, Angers.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

Nowadays in France, the standards of hospital rooms are being questioned in view of the particularities of certain populations admitted to hospitals. The " Groupement de Coopération Sanitaire des Hôpitaux Universitaires du Grand Ouest " (GCS HUGO) proposes to improve the quality of geriatric care through the… Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
User Experience
What is being tested?
User experience
How many people
120 participants
Where
No sites listed yet
Study dates
1 Dec 2021to 1 Dec 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Admissions to the Hospi'Senior room are made as the service operates, without prior selection of patients admitted. The study is proposed to : i) patients admitted to the Hospi'Senior room, ii) informal caregivers of patients admitted to the Hospi'Senior room, and iii) caregivers who have worked in the Hospi'Senior room.

Who may be able to join

  • Patient :
  • Being admitted to Hospi'Senior room
  • Informal caregiver :
  • Be the informal caregiver of a patient admitted to Hospi'Senior room (only one caregiver per patient)
  • Age ≥ 18 years old
  • Able to visit the patient admitted to Hospi'Senior room
Show all 13Show fewer
  • Caregiver :
  • Age ≥ 18 years old
  • Be a healthcare professional involved in the short-term geriatric unit, from one of 4 categories:
  • physicians,
  • permanent paramedical caregivers (nurse, nurse's aide, health executive),
  • support paramedical staff (psychologist, neuropsychologist, physiotherapist, adapted physical activity teacher),
  • technical staff (stretcher bearer).

Who cannot join

  • Patient :
  • Contraindication to participation in the study at the discretion of the medical team
  • Refusal to participate
  • Poor understanding of the French language
  • Persons deprived of liberty by an administrative or judicial decision, persons under forced psychiatric care, adults under legal protection or unable to express their consent
  • Informal caregiver :
Show all 13Show fewer
  • Refusal to participate
  • Poor understanding of the French language
  • Persons deprived of liberty by an administrative or judicial decision, persons under forced psychiatric care, adults under legal protection
  • Caregiver :
  • Be a staff in training
  • Less than 3 months seniority in the unit
  • Refusal to participate

Trial locations and contacts

No sites are listed yet.

Cédric ANNWEILER, MD,PhD contact

0241354725 ext. +33

cedric.annweiler@chu-angers.fr

About this study

Official title: Hospi'Senior : Evaluation of the User Experience of an Innovative Hospital Room Prototype Adapted to the Elderly

Nowadays in France, the standards of hospital rooms are being questioned in view of the particularities of certain populations admitted to hospitals.

The " Groupement de Coopération Sanitaire des Hôpitaux Universitaires du Grand Ouest " (GCS HUGO) proposes to improve the quality of geriatric care through the modernisation of hospital rooms.

Read more

The GCS HUGO has launched a project to co-design a hospital room adapted to the elderly, called "Hospi'Senior", with the help of the "Dependency and Old Age" steering committee. This committee is made up of experts from HUGO and partner companies.

The Hospi'Senior room is composed of innovative technologies concerning bed equipment (e.g. bed canopy), autonomous (e.g. lifeline) and assisted mobility (e.g. rail lift system), lighting (e.g. light guide), communication (touch tablet) and social space (furniture).

The project consists in evaluating the user experience (UX) of :

  • patients hospitalized in the Hospi'Senior room,
  • informal caregivers of patients hospitalized in the Hospi'Senior room,
  • caregivers who have worked in the Hospi'Senior room.
Read the detailed description

The specificities of Hospi'Senior room are multiple and concern in particular :

  • The equipment of the bed :to create a more personalized room: presence of a bed canopy, orientation of the bed towards the windows, presence of a multifunctional space at the head of the bed.
  • The autonomous mobility of the patient by facilitating the movements and by preserving the orientation in time of the patient: ephemeris for the temporal orientation, lifeline and sliding door.
  • Caregiver-assisted mobility to facilitate patient movements: lifting rail above the bed.
  • Lighting to ensure safe movement, especially during the night: light guide, room light, window mirrors, bathroom lighting.
  • The digital interface with a touch tablet to improve the occupational and communication aspects.
  • The socialization space to welcome visitors in the room.

Design:

Step 1: A visit to the room is made to each participant (patients, informal caregivers, caregivers).

Step 2: no change in care or support for users during hospitalization

Step 3: UX assessment:

  • Patients: collected at the end of the hospitalization,
  • Informal caregivers: collected at the end of the patient's stay,
  • Caregivers: collected after 3 months of using the Hospi'Senior room.
Conditions
User Experience
Being tested
User experience
Keywords
elderly, hospital room, innovation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • User experienceOther

    User experience is assessed by validated scale

Study groups in NCT05126212
Study groupRoleWhat they receive
PatientsPatients admitted to the Hospi'Senior room
Receives: Other: User experience
Informal caregiversInformal caregivers of patients admitted to the Hospi'Senior room
Receives: Other: User experience
CaregiversCaregivers who have worked in the Hospi'Senior room
Receives: Other: User experience

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. User experience of patients (AttrakDiff)

    User experience of the Hospi'Senior room is assessed by Attrakdiff scale (20 items)

    Measured: at the end of hospitalization, an average of 9 days

  2. User experience of patients (meCUE)

    User experience of the Hospi'Senior room is assessed by meCUE (Modular Evaluation of key Components of User Experience) scale module 2 (8 items)

    Measured: at the end of hospitalization, an average of 9 days

Secondary outcomes (9)
  1. User experience of informal caregivers (Attrakdiff)

    User experience of the Hospi'Senior room is assessed by Attrakdiff scale (20 items)

    Measured: at the end of hospitalization, an average of 9 days

  2. User experience of informal caregivers (meCUE)

    User experience of the Hospi'Senior room is assessed by meCUE scale module 2 (8 items)

    Measured: at the end of hospitalization, an average of 9 days

  3. User experience of caregivers (AttrakDiff)

    User experience of the Hospi'Senior room is assessed by Attrakdiff scale (20 items)

    Measured: after 3 months of using the Hospi'Senior room

  4. User experience of caregivers (meCUE)

    User experience of the Hospi'Senior room is assessed by meCUE scale module 2 (8 items)

    Measured: after 3 months of using the Hospi'Senior room

  5. User experience of patients and informal caregivers of each equipment

    User experience of each equipment is assessed by meCUE module 1 (5 items)

    Measured: at the end of hospitalization, an average of 9 days

  6. User experience of caregivers of each equipment

    User experience of each equipment is assessed by meCUE module 1 (5 items)

    Measured: after 3 months of using the Hospi'Senior room

  7. Safety aspect of "mobility" and "lighting" equipment

    Safety aspect is assessed by QUEST (Quebec User Evaluation of Satisfaction with assistive Technology) scale for patients and informal caregivers

    Measured: at the end of hospitalization, an average of 9 days

  8. Safety aspect of "mobility" and "lighting" equipment

    Safety aspect is assessed by QUEST scale for caregivers

    Measured: after 3 months of using the Hospi'Senior room

  9. Felt affects by caregivers

    Felt affects are assessed by PANAS (Positive And Negative Affect Schedule) scale (20 items)

    Measured: after 3 months of using the Hospi'Senior room

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Nov 2021
  2. Study start1 Dec 2021 (estimated)
  3. Primary completion1 Dec 2023 (estimated)
  4. Study completion1 Dec 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
120 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05126212
Sponsor's protocol ID
2021-127
Acronym
HospiSenior-UX
Status last verified
Oct 2021
First submitted
6 Oct 2021
Last updated
18 Nov 2021
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of User Experience, run by University Hospital, Angers.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 13 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 18 Nov 2021. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Cédric ANNWEILER, MD,PhD (0241354725 ext. +33, cedric.annweiler@chu-angers.fr), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

User experience of patients (AttrakDiff) (time frame: at the end of hospitalization, an average of 9 days). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Nov 2021.

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