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An observational study to investigate utility and issue of a platform that performs the online examination with monitoring using digital devices, online instruction on the use of drugs and delivering drugs for patients with Parkinson's disease

An observational study to investigate utility and issue of a platform that performs the online examination with monitoring using digital devices, online instruction on the use of drugs and delivering drugs for patients with Parkinson's disease

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1080225200
Enrollment
30
Registered
2020-05-22
Start date
2020-07-13
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson's disease

Interventions

Sponsors

Takeda Pharmaceutical Company Limited
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The participant is capable of operating each device used in this study, and understanding and complying with protocol requirements, in the opinion of the investigator. 2. The participant signs and dates a written, informed consent form prior to the initiation of any study procedures. 3. The participant has been diagnosed with Parkinson's disease on the basis of standardized diagnostic criteria. 4. The participant has some difficulty in visiting the outpatient clinic, and it is preferable to conduct online examination, online instruction on the use of drugs, and delivering drugs as part of regular care, in the opinion of the investigator. 5. The participant is a resident of Kanagawa Prefecture. 6. The participant is aged 20 years or older at the time of informed consent. 7. The participant is capable of visiting the outpatient clinic during the evaluation period.

Exclusion criteria

Exclusion criteria: 1. The participant has metal allergy. 2. The participant has cognitive impairment that, in the opinion of the investigator, would interfere with the ability to report on symptoms and function. 3. The participant has unstable Parkinson's disease and co-morbidities. 4. The participant is judged by the investigator as being ineligible for any other reason.

Design outcomes

Primary

MeasureTime frame
other Patient satisfaction with examination and instruction on the use of drugs (Client Satisfaction Questionnaire 8 [CSQ-8]) Time Frame: Week 0, 4 and 16

Secondary

MeasureTime frame
other Satisfactions and issues with the platform (using questionnaire filled by patients, caregivers, physicians, medical office work divisions of the medical institutions, and pharmacists) Time Frame: Week 16

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026