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Rehabilitation exercises delivered remotely

Researchers are testing two months of remote rehabilitation for people with neurological conditions, including Parkinson's.

Testing a treatment or activity · Study reference: JPRN-UMIN000055273

Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓

This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.

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Results reported

Start (reported date)
2024-12-01
Study finished (reported date)
2029-03-31

Planned dates can move. A study finishing does not tell us when a paper will be published.

Read the results reported in the registry

Changes we have recorded
  • 2026-10-11 — recruiting

These are dates we observed a change, not necessarily the dates it happened.

Papers connected to this study

No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.

Who can join?

Age 40years-old and over · Ask the team who can join

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Read all the rules for taking part

Sex eligibility reported by registry: male and female

Inclusion criteria: 1. Patients who have given written consent to participate in the research 2. 40 years of age or older 3a. For patients with Parkinson's disease, those diagnosed with probable PD or clinically established PD according to MDS criteria and HY stage 2-4 at the time of enrolment. 3b. For patients with mild dementia, those with MMSE less than 26 and greater than 17 and independent in activities of daily living except bathing. Background disease will be classified according to the revised NIA/AA diagnostic criteria (Alzheimer's disease) and the clinical diagnostic criteria for the prodromal DLB study (dementia with Lewy bodies), and those who are difficult to classify according to both will be classified as MCI unclassifiable (MCI-Dz). 3c. For patients with Parkinson's disease and dementia in the prodromal phase, those who meet some of the diagnostic biomarkers and diagnostic criteria for each disease listed above and are expected to develop the disease in the future. 4. Patients who have the cooperation of a caregiver 5. Patients who are able to walk a stable 10m with the use of assistive devices such as prostheses and walking sticks. 6. Patients who have been taking a fixed dose of antiparkinsonian or antidementia medication for at least two months prior to enrolment 7. Patients who be able to understand verbal instructions and perform tasks adequately Exclusion criteria: 1. Patients with severe cognitive impairment (<16 points on MMSE) 2. Patients with unstable general condition, including vital signs 3. Patients with severe visual impairment (corrected binocular vision below 0.05). 4. Patients who are pregnant, lactating or may become pregnant. 5. Patients with pre-existing or concomitant clinically relevant neuropsychiatric disorders (e.g. patients requiring adjustment of antipsychotic medication) 6. Patients who have participated in other motor function intervention studies within 6 months prior to enrolment 7. Patients who are difficult to assess at each visit due to unpredictable wearing-off or On-off symptom. 8. Patients with osteoarticular complications such as lumbar spinal stenosis or back pain that affect motor assessment 9. Patients who are deemed by the investigator to be unsuitable for the study.
Full study name & original research details

Official study title

Development of a Remote Rehabilitation System to Enhance Physical Activity in Patient with Neurodegenerative Diseases - Remote Rehab Research for Neurodegenerative Diseases

Short title used by the registry

Development of a Remote Rehabilitation System to Enhance Physical Activity in Patient with Neurodegenerative Diseases

Original description

Intervention: 2 months of voluntary exercise training and guidance using a remote rehabilitation system Primary outcome: Subjective satisfaction scale Secondary outcome: All adverse events. System Usability Scale (SUS), exercise adherence (number of participants achieving acceptable adherence (>60%) and ideal adherence (>80%)), daily physical activity (physical activity, moderate- and high-intensity physical activity), balance and gait assessment (10 m - walking speed, Mini- BESTest, 3m-TUG test), change in upper limb function assessment (box and block test), change in motor features of Parkinson's disease (MDS-UPDRS, FOGQ), change in quality of life assessment (WHO-QOL, PDQ8), and change in functional/ structural MRI at the 2-month and 4-month visits compared with baseline.

Conditions reported: Patients with neurodegenerative disease (especially, Parkinson's disease and dementia), and those in the prodromal phase of the disease

Registry records for this study

Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.

Study type
Interventional
Interventions
2 months of voluntary exercise training and guidance using a remote rehabilitation system
Phases
Not selected
Sponsor
Kawasaki Medical School
Start date reported by registry
2024-12-01 (reported)

Registry updated: Not reported · Status last verified by the registry submitter: Not reported

Registry records retrieved 2026-10-11 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.

Contact the research team

Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.

Mihara Masahito · 0864621111 · neuro-office@med.kawasaki-m.ac.jp

Study locations

Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.

Facility not reported

Japan

Status not reported

The original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.