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NCT Number: NCT04087031

Innovative Models in the Rehabilitation of the Elderly With Parkinson's Disease Through Technological Innovation

The final goal of the present study is to propose a new approach in the Parkinson's Disease rehabilitation, focused on the use of robotic devices and to check the results not only at the end of the treatment but also in the long term, foreseeing 3 follow-up.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

IRCCS INRCA Hospital, Ancona, Italy

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About this study

Parkinson's disease is one of the most frequent causes of disability among the elderly. It is a chronic-progressive neuro-degenerative disease, characterized by several motor disorders. The balance disorder is a symptom that involves the body axis; it is due to a reduction in the straightening reflexes, so the subject is not able to correct any imbalances. Balance disorders do not respond to dopaminergic therapy used in Parkinson's disease. Therefore, physiotherapy becomes an important intervention for the management of motor disorders. Originally, these rehabilitative approaches were based on empirical experiences, but several scientific evidence suggests that neuronal plasticity is exercise-dependent. In this context, robotic rehabilitation performs an important role because it allows to perform task-oriented exercises and to increase the number of repetitions and their intensity. This protocol study aims to evaluate an innovative rehabilitation treatment of the elderly patients with Parkinson's disease, designed to improve the gait and to reduce the risk of falling. The treatment involves the use of two robotic devices: Tymo system and Walker View.

This study is a single-blinded randomized controlled trial. 195 patients with PD will be recruited and randomly divided into three groups, to receive a traditional rehabilitation program or a robotic rehabilitation using Tyro system or Walker View in addition to the traditional therapy. Assessments will be performed at baseline, at the end of treatment and 6 months, 1 year and 2 years from the end of the treatment. A 10 treatment sessions will be conducted, divided into 2 training sessions per week, for 5 weeks. The control group will perform traditional therapy sessions lasting 50 minutes. The technological intervention group will carry out 30 minutes of traditional therapy and 20 minutes of treatment with a robotic system.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Hoen and Yahr scale: 1-3 stage
  • FAC ≤ 2
  • Ranking scale score ≤ 3
  • Stability of drug treatment for at least 1 month
  • Geriatric Depression Scale 5-items: negative

Exclusion criteria

  • Concomitant participation in other studies
  • Lack of written informed consent
  • Clinical dementia rating (CDR) score ≥ 3
  • History of syncopal episodes, epilepsy and vertigo not controlled pharmacologically
  • Serious dysfunction of the autonomic system
  • Severe behavioral syndromes not compensated by drugs
  • Concurrent neurological diseases
  • Severe systemic diseases with life expectancy < 1 year
  • Patients unable to follow up.

Treatment and study plan

Control Arm

Other

Each session will include 50 minutes of traditional physical rehabilitation therapy

Virtual Reality games

Other

Each session will include 30 minutes of traditional physical rehabilitation therapy followed by 20 minutes of robotic Tymo system (Tyromotion, Austria), a wireless static and dynamic platform, for evaluating and rehabilitating posture.

robotic treadmill

Other

Each session will include 30 minutes of traditional physical rehabilitation therapy followed by 20 minutes of robotic Walker View (TecnoBody, Italy) a treadmill equipped with a sensorized belt with eight load cells and a 3D camera

Primary outcomes

  1. difference in falling risk among virtual reality games arm, robotic treadmill arm and control arm

    Time frame: before treatment, at the end of treatment and 6, 12 and 24 months after the end of treatment

    falling risk will be evaluated by the Tinetti performance oriented mobility assessment (POMA). POMA test has two subscales, Balance and Gait sections. Total score is obtained by adding the scores of the two subscales (balance + gait) . Total score < 19 high fall risk, total score 19-24 medium fall risk, total score 25-28 low fall risk.

Secondary outcomes

  1. difference in gait performance among virtual reality games arm, robotic treadmill arm and control arm

    Time frame: before treatment, at the end of treatment and 6, 12 and 24 months after the end of treatment

    gait performance will be assessed by walking speed through instrumental Gait Analysis

  2. difference in fear of falling among virtual reality games arm, robotic treadmill arm and control arm

    Time frame: before treatment, at the end of treatment and 6, 12 and 24 months after the end of treatment

    fear of falling will be evaluated by the Falls Efficacy Scale - International (FES-I). Higher scores represent greater the fear of falling (ranging from 16 to 64)

Study contacts

Contact information is provided by the study sponsor or research team.

Roberta Bevilacqua

CONTACT

[email protected]

00390718004767

Sponsors and collaborators

Lead sponsor

Istituto Nazionale di Ricovero e Cura per Anziani

Other

Registry information

Official study title

Assistive Robotic in the Elderly: Innovative Models in the Rehabilitation of the Elderly With Parkinson's Disease Through Technological Innovation

Important dates

Study start
2019
Primary completion
2026
Study completion
2026
First posted
Sep 12, 2019
Registry last updated
Oct 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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