LET’S BUILD THE FUTURE OF TELEREHABILITATION TOGETHER

Small and compact

Easy to sanitise

Convenient charging method

Easy to operate

Ready to use!

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ARC intellicare is certified as a Class I Medical Device according to MDR 2017/745.

ARC’s wearable sensors are compliant with biocompatibility standards (ISO10993). The charging base and all electronic components of ARC comply with IEC60601-1 (electrical safety), IEC 60601-1-2 (electromagnetic compatibility) standards and IEC60601-1-11 (safe for home use).

FEATURES AND FUNCTIONALITIES

Validated rehabilitation protocols
Thanks to collaboration with healthcare professionals, ARC offers a wide library of exercises validated based on standard clinical practice.

Adherence monitoring
ARC intellicare allows monitoring of adherence to the rehabilitation plan, thanks to an innovative artificial intelligence algorithm (in the patententing phase).

Integrated audio-video channel
ARC allows viewing and listening to video tutorials of the exercises to be performed. The video call function allows the therapist to contact the patient when necessary, or for control calls during usage of the device.

Personalised programmes of exercises
The exercises made available by ARC can be combined to create a personalised rehabilitation plan according to the needs of each patient.

Numerical rating scales
At the end of each group of exercises, the patient leaves a rating based on the three scales of discomfort, fatigue, and general health to provide feedback on their physical condition.

GDPR compliance
ARC guarantees a high level of security and protection of personal data of users. The system is designed in compliance with GDPR and the European Medical Devices Regulation MDR 2017/745.

FEATURES AND FUNCTIONALITIES

Validated rehabilitation protocols
Thanks to collaboration with healthcare professionals, ARC offers a wide library of exercises validated based on standard clinical practice.

Adherence monitoring
ARC intellicare allows monitoring of adherence to the rehabilitation plan, thanks to an innovative artificial intelligence algorithm (in the patententing phase).

Integrated audio-video channel/b>
ARC allows viewing and listening to video tutorials of the exercises to be performed. The video call function allows the therapist to contact the patient when necessary, or for control calls during usage of the device.

Personalised programmes of exercises
The exercises made available by ARC can be combined to create a personalised rehabilitation plan according to the needs of each patient. Numerical rating scales
At the end of each group of exercises, the patient leaves a rating based on the three scales of discomfort, fatigue, and general health to provide feedback on their physical condition. GDPR Compliance
ARC guarantees a high level of security and protection of personal data of users. The system is designed in compliance with GDPR and the European Medical Devices Regulation MDR 2017/745.

ARTIFICIAL INTELLIGENCE FOR REHABILITATION

THE innovativE ARTIFICIAL INTELLIGENCE ALGORITHM:

Recognises motor exercises, even complex ones (e.g. bilateral with alternating movement)

Does not require any sensor calibration

Has been validated through clinical studies and is in the patenting phase

this allows:

Patients to know in real time the number of repetitions correctly performed

Healthcare professionals to verify that the patient performs the exercises appropriately even at home, without their direct supervision

CLINICAL STUDIES

Two feasibility studies have shown that ARC intellicare can be adopted in clinical practice and is easily integrated into ambulatory, home-based, or mixed rehabilitation pathways.

The results of these studies confirm the ease of use of ARC by patients with neurological, motor, and respiratory difficulties, particularly in elderly subjects, with great satisfaction for rehabilitation professionals and caregivers.

ARCANGEL STUDY

Clinical study ID NCT03787433 (pre-commercial procurement MAGIC)

Experimental centres: ASL TO3, Pinerolo (TO), Northern Health and Social Care Trust, Northern Ireland (UK).

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ARCTRAN STUDY

Randomised controlled clinical study

Experimental centre: Agostino Gemelli University Polyclinic IRCSS in Rome, Neurology Unit.

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RICOMINCIARE STUDY

Clinical study ID NCT05074771 (POR-FESR 2014-2020 Emilia-Romagna Region)

Experimental centre: Polytechnic University of Marche.

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