Efficacy of Proprioceptive Focal Stimulation (EQUISTASI) on Gait Parameters in Parkinson. Italian Multicentric Study (PAGE)
Primary Purpose
Parkinson Disease, Gait, Shuffling, Effects of Vibration
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Equistasi
Inactive Equistasi
Sponsored by
About this trial
This is an interventional treatment trial for Parkinson Disease focused on measuring Gait analysis, Proprioceptive focal stimulation, Parkinson
Eligibility Criteria
Inclusion Criteria:
- Patient with rigid-acinetic bilateral PD form
- At least 4 years of disease history
- H&Y between 2-3
- Stable drug therapy response without any change performed in the 3 months before the study.
- Presence of freezing (FOG) and of postural instability not responding to parkinsonian therapy.
- MMSE>24/30 (Mini-Mental State Examination)
Exclusion Criteria:
- Systemic illness
- Presence of cardiac pacemaker
- Presence of deep brain stimulation
- Presence of severe dysautonomia with marked hypotension
- Obsessive-Compulsive disorder (OCD)
- Major depression
- Dementia
- History or active neoplasia
- Pregnancy
Sites / Locations
- IRCCS Santa Lucia
- IRCCS National Neurological Institute "C. Mondino" Foundation
- Istituto Auxologico Italiano
- IRCCS San Raffaele
- University of Genova
- Ospedale S. Raffaele Arcangelo, Fatebenefratelli
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Equistasi
Placebo
Arm Description
Equistasi is a nanotechnology for proprioceptive focal stimulation. Every patient will receive three patches to be placed at C7 and at the gastrocnemial junction of both legs.
Inactive Equistasi will be given to every patient in the form of three patches to be placed at C7 and at the gastrocnemial junction of both legs.
Outcomes
Primary Outcome Measures
Changes in Spatio-Temporal gait variables at 20 weeks
Secondary Outcome Measures
Changes in the Movement Disorder Society - Unified Parkinson Disease Rating Scale (MDS-UPDRS) - at 20 weeks
Changes in the Parkinson Disease 39 Questionnaire (PDQ-39) at 20 weeks
Changes in the Activity Specific Balance Confidence Scale (ABC scale) at 20 weeks
Full Information
NCT ID
NCT02641405
First Posted
December 3, 2015
Last Updated
January 9, 2021
Sponsor
I.R.C.C.S. Fondazione Santa Lucia
Collaborators
Istituto Auxologico Italiano, IRCCS National Neurological Institute "C. Mondino" Foundation, Ospedale S. Raffaele Arcangelo, Fatebenefratelli, University of Genova, IRCCS San Raffaele
1. Study Identification
Unique Protocol Identification Number
NCT02641405
Brief Title
Efficacy of Proprioceptive Focal Stimulation (EQUISTASI) on Gait Parameters in Parkinson. Italian Multicentric Study
Acronym
PAGE
Official Title
Efficacy of Proprioceptive Focal Stimulation (EQUISTASI) on Gait Parameters in Parkinson. Italian Multicentric Study
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
November 2015 (Actual)
Primary Completion Date
January 2019 (Actual)
Study Completion Date
January 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
I.R.C.C.S. Fondazione Santa Lucia
Collaborators
Istituto Auxologico Italiano, IRCCS National Neurological Institute "C. Mondino" Foundation, Ospedale S. Raffaele Arcangelo, Fatebenefratelli, University of Genova, IRCCS San Raffaele
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
It's already known the efficacy of Gait Analysis (GA) on evaluating gait modification on Parkinson's Disease (PD) Patients (1). On the other hand Proprioceptive Focal Stimulation seems be useful in symptoms amelioration in several neurological disease. Few studies have been performed in Parkinson's disease. A total of 126 patients suffering from PD will be recruited in 6 italian neurological centers. The study will be a cross-over multicenter study with the randomization of the sequence. The patients will be randomly assigned to 2 groups receiving for 8 weeks either the Equistasi medical device, or an equivalent placebo. Gait analysis will be recorded in each patient at the beginning and at the end of the treatment assigned. After 4 weeks of wash-out, the treatment will be crossed and a new gait analysis recording will be performed. Finally a last recording will be taken at the end of the last 8 weeks. Secondary outcome will be the MDS-UPDRS (Movement Disorder Society - Unified Parkinson Disease Rating Scale), PDQ-39 (Parkinson Disease 39 Questionnaire ), ABC (Activity Specific Balance Confidence Scale).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease, Gait, Shuffling, Effects of Vibration
Keywords
Gait analysis, Proprioceptive focal stimulation, Parkinson
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
126 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Equistasi
Arm Type
Experimental
Arm Description
Equistasi is a nanotechnology for proprioceptive focal stimulation. Every patient will receive three patches to be placed at C7 and at the gastrocnemial junction of both legs.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Inactive Equistasi will be given to every patient in the form of three patches to be placed at C7 and at the gastrocnemial junction of both legs.
Intervention Type
Device
Intervention Name(s)
Equistasi
Intervention Description
Equistasi is a nanotechnology for proprioceptive focal stimulation. Every patient will receive three patches to be placed at C7 and at the gastrocnemial junction of both legs.
Intervention Type
Device
Intervention Name(s)
Inactive Equistasi
Intervention Description
Inactive Equistasi will be given to every patient in the form of three patches to be placed at C7 and at the gastrocnemial junction of both legs.
Primary Outcome Measure Information:
Title
Changes in Spatio-Temporal gait variables at 20 weeks
Time Frame
20 weeks
Secondary Outcome Measure Information:
Title
Changes in the Movement Disorder Society - Unified Parkinson Disease Rating Scale (MDS-UPDRS) - at 20 weeks
Time Frame
20 weeks
Title
Changes in the Parkinson Disease 39 Questionnaire (PDQ-39) at 20 weeks
Time Frame
20 weeks
Title
Changes in the Activity Specific Balance Confidence Scale (ABC scale) at 20 weeks
Time Frame
20 weeks
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient with rigid-acinetic bilateral PD form
At least 4 years of disease history
H&Y between 2-3
Stable drug therapy response without any change performed in the 3 months before the study.
Presence of freezing (FOG) and of postural instability not responding to parkinsonian therapy.
MMSE>24/30 (Mini-Mental State Examination)
Exclusion Criteria:
Systemic illness
Presence of cardiac pacemaker
Presence of deep brain stimulation
Presence of severe dysautonomia with marked hypotension
Obsessive-Compulsive disorder (OCD)
Major depression
Dementia
History or active neoplasia
Pregnancy
Facility Information:
Facility Name
IRCCS Santa Lucia
City
Rome
State/Province
Lazio
ZIP/Postal Code
00179
Country
Italy
Facility Name
IRCCS National Neurological Institute "C. Mondino" Foundation
City
Pavia
State/Province
PV
Country
Italy
Facility Name
Istituto Auxologico Italiano
City
Oggebbio
State/Province
Verbano-Cusio-Ossola
ZIP/Postal Code
28824
Country
Italy
Facility Name
IRCCS San Raffaele
City
Cassino
Country
Italy
Facility Name
University of Genova
City
Genova
Country
Italy
Facility Name
Ospedale S. Raffaele Arcangelo, Fatebenefratelli
City
Venezia
ZIP/Postal Code
30121
Country
Italy
12. IPD Sharing Statement
Learn more about this trial
Efficacy of Proprioceptive Focal Stimulation (EQUISTASI) on Gait Parameters in Parkinson. Italian Multicentric Study
We'll reach out to this number within 24 hrs