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Clinical Trials/NCT04176302
NCT04176302
Completed
N/A

Monitoring of Mobility of Parkinson's Patients for Therapeutic Purposes - Clinical Trial

Consorci Sanitari de l'Alt Penedès i Garraf43 sites in 1 country173 target enrollmentNovember 26, 2019

Overview

Phase
N/A
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
Consorci Sanitari de l'Alt Penedès i Garraf
Enrollment
173
Locations
43
Primary Endpoint
Daily time in Off
Status
Completed
Last Updated
4 months ago

Overview

Brief Summary

When Parkinson Disease is mild, it responds well to treatment with drugs (L-Dopa and dopamine antagonists). However, as the disease progresses, the effect of the drugs diminishes and lasts for a shorter time (wearing-off), which require physicians to progressively increase and/or break up the dosage of dopamine drugs, to control symptoms over the course of the entire day. Despite this, most patients present motor fluctuations after 10 years. These fluctuations consist of changes between what are known as Off periods, when the medication does not produce an effect and mobility is hindered, and On periods when patients can move smoothly, with the medication producing its best effect.

The timeline of these motor fluctuations over the course of the day and also on different days is very valuable to precisely adjust the medication. Nevertheless, neurologists do not currently have detailed information on the timeline of the symptoms of their patients, which means that they have serious difficulties to obtain good results with the adjustment of medication. Currently, the neurologist's information on the time progression of the motor fluctuations is drawn from what the patient indicates in the office visit, or in the best case, from diaries that the patient fills out at home, periodically (e.g. every hour) noting the motor state (On or Off). Although the latter method is still the gold standard in research and in care, it has serious limitations, because patients often forget to record the information (especially when they are in Off), many do not recognize their motor states well, and few can maintain adherence to such a laborious system for more than a few days.

The Parkinson Holter (STAT-ON ®) is a wearable device, which objectively measures and records the motor fluctuations of the patients. It does not require intervention by the patient, and can, therefore, be used in daily life, long term if necessary. However, the concept that detailed knowledge of motor fluctuations of patients will lead to better control of the disease, thanks to optimisation of the therapeutic regimen, is still a hypothesis. To demonstrate or refute this hypothesis, we are now conducting a clinical trial, with this medical device, to study the clinical effectiveness in patients with moderate Parkinson's disease and motor fluctuations. This trial will show whether using the Parkinson Holter is better than the clinical interview used in traditional clinical practice (primary objective), and whether it is not inferior to the On-Off diary recorded by the patients at home (exploratory objective)

Registry
clinicaltrials.gov
Start Date
November 26, 2019
End Date
June 21, 2023
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Consorci Sanitari de l'Alt Penedès i Garraf
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Ideopathic Parkinson's Disease
  • Disease in the moderate-severe phase (Hoehn \& Yahr ≥ 2 en Off)
  • Motor fluctuations (with at least 2h/day in Off)
  • Agree to participate voluntarily and will sign a written consent form

Exclusion Criteria

  • Incapable of walking independently or H\&Y=5
  • Participating in another clinical trial
  • Patients with acute intercurrent disease
  • Psychiatric or cognitive disorders that prevent collaboration (MMSE \<24)

Outcomes

Primary Outcomes

Daily time in Off

Time Frame: 7 days

Changes from baseline to last visit in daily hours in Off

Secondary Outcomes

  • Reported quality of life(1 month)
  • System usability: System Usability Scale(7 days)
  • Motor complications(6 months)
  • Change of presence and severity of freezing of gait episodes(7 days)
  • Number of clinical contacts(6 months)
  • Patient's adherence to the MF measurement system(7 days)
  • Number of therapeutic changes.(6 months)
  • Daily time in On(7 days)
  • User satisfaction: Quebec User Evaluation of Satisfaction with assistive Technology(7 days)
  • Activities of Daily Living(6 months)

Study Sites (43)

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