Parkinson Holter
DeviceThe neurologists will receive the wearable report (for medication adjustment, if any as per physician's criteria/judgement)
Other names: STAT-ON ® sensor
NCT Number: NCT04176302
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)
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Hospital Universitari Vall d'Hebron, Barcelona, Spain
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The neurologists will receive the wearable report (for medication adjustment, if any as per physician's criteria/judgement)
Other names: STAT-ON ® sensor
The neurologists will receive the patient's diary report (for medication adjustment, if any as per physician's criteria/judgement).
Other names: Parkinson's diary
The neurologists will receive the patient & caregiver report at the time of the visit (for medication adjustment, if any as per physician's criteria/judgement).
Other names: Clinical interview
Time frame: 7 days
Changes from baseline to last visit in daily hours in Off
Time frame: 6 months
Number of patient visits and telephone controls to adjust medication
Time frame: 7 days
Total hour/days with information registered.
Time frame: 6 months
Number of therapeutic changes done to improve symptoms.
Time frame: 6 months
Changes from baseline to last visit in motor complications, assessed by means of Unified Parkinson's Disease Rating Scale - part IV
Time frame: 7 days
Changes from baseline to last visit in daily hours in On
Time frame: 7 days
Changes from baseline to last visit in the number and severity of freezing of gait episodes, assessed by means of Freezing of Gait Questionnaire
Time frame: 1 month
Changes from baseline to last visit in quality of life, assessed by menas of Parkinson's Disease Questionnaire-39
Time frame: 6 months
Changes from baseline to last visit in dependence for Activities of Daily Living assessed by means of Unified Parkinson's Disease Rating Scale - part II
Time frame: 7 days
Physician and patient satisfaction with the Parkinson Holter will be assessed by means of the Quebec User Evaluation of Satisfaction with assistive Technology (QUEST)
Time frame: 7 days
Usability of the system will be assessed by System Usability Scale (SUS)
Consorci Sanitari de l'Alt Penedès i Garraf
Other
Acronym: MoMoPa-EC
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