Evaluation of the Uses of a Digital-assisted Self-rehabilitation Device (TELE-PARK)

NCT ID: NCT03667456

Last Updated: 2020-07-27

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

COMPLETED

Clinical Phase

NA

Total Enrollment

31 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-06-11

Study Completion Date

2020-06-26

Brief Summary

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Evaluate the use by the patient and his family and professional environment of a self-rehabilitation device with follow-up in tele-rehabilitation in people with Parkinson's disease taking into account the different actors within a health area (health professionals and paramedics in structure and in liberal).

Detailed Description

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Conditions

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Parkinson Disease Parkinson's Syndrome

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Self-rehabilitation by digital support

Provision to patients selected by doctors or physiotherapists of an interactive digital tool (tablet + inertial sensor) to support self-rehabilitation home Parkinson's patients.

Monitoring and regulation of remote self-reeducation by tele-reeducation. Evaluation of the acceptance of the tool and the quality of life of the patients by questionnaire at day 0, and two and twelve months after.

Group Type EXPERIMENTAL

Self-rehabilitation by digital support

Intervention Type PROCEDURE

Provision to patients selected by doctors or physiotherapists of an interactive digital tool (tablet + inertial sensor) to support self-rehabilitation home Parkinson's patients.

Interventions

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Self-rehabilitation by digital support

Provision to patients selected by doctors or physiotherapists of an interactive digital tool (tablet + inertial sensor) to support self-rehabilitation home Parkinson's patients.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

Patients:

* Men and women over the age of 18
* With Parkinson's syndrome due to idiopathic Parkinson's disease or related syndromes
* Presenting a complaint about balance and/or walking
* With possible walking over a perimeter of at least 100 meters with or without technical aid
* Hoehn and Yahr scale \< or = to 4
* Formulating their free and informed consent in writing.

Health professionals:

\- physiotherapists and physiatrists hospital or voluntary volunteers practicing in the territory of health 5 in Brittany agreeing to participate in the study

Exclusion Criteria

* Orthopedic and rheumatologic pathologies that may prevent the achievement of measures
* Comprehension disorders preventing the implementation of the protocol
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Réseau Parkinson Bretagne

UNKNOWN

Sponsor Role collaborator

Rennes University Hospital

OTHER

Sponsor Role collaborator

Pôle Saint Hélier

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Philippe Gallien, Doctor

Role: STUDY_DIRECTOR

Pole Saint Hélier

Locations

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Pôle Saint Hélier

Rennes, Brittany Region, France

Site Status

Countries

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France

Other Identifiers

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2017-A02379-44

Identifier Type: -

Identifier Source: org_study_id

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