NCT04091152

Brief Summary

In the last ten years, gerontechnology is becoming an increasing topic in geriatric medicine. Nevertheless, there are still few studies assessing the usability of technologies in old patients, especially when they are hospitalized. Moreover, it has been shown that new technologies could be a source of ageism, thence the importance of involving the old people in the development of these technologies. Tik easy is a subsidiary of La Poste Company. Tik easy as designed a new tablet PC for old people. Research tends to show that the use of tablet PC can promote health and well-aging, and delay cognitive decline. In this study, we want to give a free access to "Ardoiz", the tablet PC designed by Tik easy, for old patients hospitalized in a geriatric acute care unit. The "Ardoiz" tablet PC allows to:

  • Maintain the family and social bond (send and receive messages, share photos and videos, call remotely between the patient and his family)
  • Discovering the Internet at his own pace (browse the Internet with daily updated contents such as news, content on cooking, music, etc.).
  • Prevent cognitive aging (stimulate cognitive abilities with the DYNSEO games).
  • Facilitate online administrative procedures.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Sep 2019

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 12, 2019

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 16, 2019

Completed
3 days until next milestone

Study Start

First participant enrolled

September 19, 2019

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 16, 2020

Completed
9 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 25, 2020

Completed
Last Updated

October 1, 2019

Status Verified

September 1, 2019

Enrollment Period

12 months

First QC Date

September 12, 2019

Last Update Submit

September 30, 2019

Conditions

Keywords

old poepleelderlyusabilityergonomytablet PC

Outcome Measures

Primary Outcomes (1)

  • Usability of the Ardoiz® tablet PC

    The usability will be assessed using the validated System Usability Scale (SUS). The mean score obtained by users will be calculated. "Ardoiz" will be considered as usable if the mean score on the SUS is equal or over 70 on 100.

    During the 48 hours before the discharge of the hospital

Secondary Outcomes (5)

  • Satisfaction of the users following the use of the Ardoiz® tablet PC.

    During the 48 hours before the discharge of the hospital

  • Frequency of use of the Ardoiz® tablet PC by elderly hospitalized patients.

    During the 48 hours before the discharge of the hospital

  • Most appreciated ergonomic elements for the users

    During the 48 hours before the discharge of the hospital

  • Improvement areas regarding the ergonomics of the Ardoiz® tablet PC.

    During the 48 hours before the discharge of the hospital

  • Improvement areas regarding the functions of the Ardoiz® tablet PC.

    During the 48 hours before the discharge of the hospital

Study Arms (3)

old patients

Patient will freely use "Ardoiz" during their hospitalisation for a maximum of 9 days. After this use, a survey concerning the usability of "Ardoiz" will be administered to the patient, before their discharge from hospital.

Other: usability assessment

relatives / unformal caregivers

Unformal caregivers will freely use "Ardoiz" during the hospitalization of their relatives and a maximum of 9 days. After this use, a survey concerning the usability of "Ardoiz" will be administered to the unformal caregivers, before the discharge of their hospitalized relatives from hospital.

Other: usability assessment

profesionnal caregivers

After the inclusion of all expected patients and relatives, a survey concerning the usability of "Ardoiz" will be administered to professional caregivers.

Other: usability assessment

Interventions

Usability of "ardoiz" will be assesse using a validated usability questionnary

old patientsprofesionnal caregiversrelatives / unformal caregivers

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients are recruited during their hospitalisation in geriatric medicine. Relatives / unformal caregivers are recruited during the hospitalisation of patients in geriatric medicine. Professionnal caregivers are recruited in the acute care geriatric unit.

You may qualify if:

  • Patients :
  • Aged 65 years old and over
  • To be hospitalised in geriatric medicine department of Angers University Hospital
  • Caregivers:
  • Family members or relatives
  • Aged 18 years old and over
  • Healthcare team :
  • geriatric medicine department's staff of Angers University Hospital
  • Aged 18 years old and over

You may not qualify if:

  • Patients :
  • Existence of a delirium revealed by the Confusion Assessment Method
  • To be under legal protection
  • Refusal of participating

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Angers University Hospital

Angers, 49933 cedex 9, France

RECRUITING

MeSH Terms

Conditions

FrailtyPersonal Satisfaction

Condition Hierarchy (Ancestors)

Pathologic ProcessesPathological Conditions, Signs and SymptomsBehavior

Study Officials

  • Cedric Annweiler, MD, PhD

    Angers University Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Cedric Annweiler, MD, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 12, 2019

First Posted

September 16, 2019

Study Start

September 19, 2019

Primary Completion

September 16, 2020

Study Completion

September 25, 2020

Last Updated

October 1, 2019

Record last verified: 2019-09

Locations