Study of the Acceptability and Psychosocial Impact of Using a Telepresence Robot in the Living Space of Inpatients (ROBOLINK-e)

Association APPROCHE

Status: Enrolling

Conditions: Motor Disorders; Cognitive Disability

Treatments: Device: Telepresence robot

Study type: Interventional

Funder types: Other

Identifiers

NCT04899830

2019-A02088-49

Details and patient eligibility

About

This study focuses on the mobile robot assist device for tele-interaction: the "COVEALINK 2" robot. This telepresence robot is designed for remote use inside the home. It works with an Internet connection (Wifi or 4G). It consists of a control interface (an application installed on the smartphone or tablet of the hospitalized patient) and a mobile robot placed in the home of the hospitalized patient (composed of a mobile platform, a visualization screen whose tilt is adjustable remotely for better adaptation to the interlocutors and an audio communication system). From the app installed on his smartphone or tablet, the patient hospitalized in the center for a long time (2 months minimum) will be able to start remotely (from the center where he is hospitalized) the robot and have it move within his home to communicate with the people present at the time of use (family, friends, neighbors etc.).

Enrollment: 16 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age ≧ 18 years old
• Affiliation to a social security scheme or beneficiary of such a scheme
• Having signed a free informed consent in writing
• Hospitalized in PRM for a foreseeable period of at least 60 days
• Living space compatible with the movement of the robot (verified by a home visit by the center's occupational therapist) and equipped with wifi
• Cognitive and motor functions compatible with the use of the tablet or phone independently, with learning capabilities to use the robot and the completion of questionnaires and interviews remotely
• Medically stable

Exclusion criteria

• Subject being in a period of exclusion from another protocol
• Mood and behavior disorders not stabilized
• Insufficient command of the French language
• Protected adults (guardianship / curatorship)
• Pregnant or breastfeeding women
• Persons deprived of their liberty
• Being unable to issue their consent
• Person who has already presented a form of addiction to technologies and / or video games

Trial design

Primary purpose: Other

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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16 participants in 1 patient group

Installation of a telepresence robot in the home of a disabled person hospitalized in a PRM center

Experimental group

Description:

From the application installed on a tablet, the patient hospitalized in a center for a period of at least 2 months can start from the center where he is hospitalized the mobile robotic telepresence assistance device installed at home to communicate with his family, his friends, his neighbors,...)

Treatment:

Device: Telepresence robot