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Mobility in Atypical Parkinsonism: a Trial of Physiotherapy (Mobility_APP)

Primary Purpose

Multiple System Atrophy, Parkinson Variant (Disorder), Parkinson Disease, Progressive Supranuclear Palsy

Status
Recruiting
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Physiotherapy
Sponsored by
Universitätsklinik für Neurologie, Innsbruck
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple System Atrophy, Parkinson Variant (Disorder)

Eligibility Criteria

30 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • The subject is willing and able to give written informed consent
  • The patient is able to tolerate all study visits including daily physiotherapy and home training.
  • Patients similar with regard to age and sex with probable/possible MSA-P according to rev. Gilman criteria OR probable/possible PSP-RS according to MDS-PSP criteria OR PD according to MDS-PD criteria.
  • Stable antiparkinsonian and Anti-OH medication 4 weeks prior to study entry.

Exclusion Criteria:

  • Co-morbidities that influence the clinical presentation of parkinsonian symptoms (as judged by the enrolling investigator).
  • Participation in other clinical trials that might influence the impact of the trial intervention (as judged by the enrolling investigator)
  • H&Y Staging score greater than or equal to 4
  • Change of antiparkinsonian and anti-OH medication 4 weeks prior to the interventional trial.
  • Secondary cause of autonomic failure or parkinsonism (e.g. diabetic autonomic neuropathy, bladder surgery, drug-induced or vascular parkinsonism, etc.)
  • Dementia according to DSM-V.

Sites / Locations

  • Medical University InnsbruckRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Physiotherapy 1

Physiotherapy 2

Arm Description

Outcomes

Primary Outcome Measures

Sensor-based analysis
To investigate whether Physiotherapy 1 versus Physiotherapy 2 and home-based exercise lead to significantly greater improvement of lab and home-based gait parameters (gait velocity, stride length, stride time, swing time, stance time, heel strike angle and maximal toe clearance measures will be aggregated to one report value) in patients with PD, MSA-P and PSP-RS.

Secondary Outcome Measures

Clinical Rating scales
To evaluate the effects of Physiotherapy 1 versus Physiotherapy 2 on motor symptoms and on different domains of patients with MSA-P, PD, and PSP-RS by means of the patients ́ questionnaires (MoCA, Frontal Assessment Battery, International Physical Activity Questionnaire, Orthostatic Hypotension Questionnaire, 8-Item Parkinson's Disease Questionnaire, Freezing of Gait Questionnaire, System Usability Scale, Berg Balance Scale, Clinical Global Impression of severity/change, Participants Global Impression of severity/change) and clinical rating scales (MDS-UPDRS, UMSARS, PSP-RS, Hoehn & Yahr).

Full Information

First Posted
October 19, 2020
Last Updated
May 10, 2023
Sponsor
Universitätsklinik für Neurologie, Innsbruck
Collaborators
University of Erlangen-Nürnberg, Germany, University Hospital Erlangen, Germany, Ecole Polytechnique Fédérale de Lausanne, Switzerland, University of Lausanne Hospital, Switzerland, Medical University Innsbruck, University of Luxembourg, Luxembourg, Hospital of Bolzani, Italy
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1. Study Identification

Unique Protocol Identification Number
NCT04608604
Brief Title
Mobility in Atypical Parkinsonism: a Trial of Physiotherapy
Acronym
Mobility_APP
Official Title
Mobility in Atypical Parkinsonism: a Randomized Trial of Physiotherapy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2021 (Actual)
Primary Completion Date
June 30, 2024 (Anticipated)
Study Completion Date
November 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universitätsklinik für Neurologie, Innsbruck
Collaborators
University of Erlangen-Nürnberg, Germany, University Hospital Erlangen, Germany, Ecole Polytechnique Fédérale de Lausanne, Switzerland, University of Lausanne Hospital, Switzerland, Medical University Innsbruck, University of Luxembourg, Luxembourg, Hospital of Bolzani, Italy

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients with atypical parkinsonism often show gait and mobility impairment manifesting in early disease stages. In order to maintain mobility and physical autonomy as long as possible for these patients, we will examine the effect of two types of physiotherapy in patients with multiple system atrophy (MSA), progressive supranuclear gaze palsy (PSP) and idiopathic Parkinson's disease (IPD). The study is divided into an ambulant daily in-patient physiotherapy phase, followed by a home-based training phase. At the beginning and the end of the study, the patients daily activity will be recorded for one week using Physical Activity Monitoring (PAM) sensors. The aim of this double-blind, randomized-controlled study is to determine effective physiotherapy in patients with atypical parkinsonian syndromes in order to maintain mobility for as long as possible.
Detailed Description
Patients with Parkinson's disease often show gait impairment and reduced mobility over the disease course. Rare atypical forms of parkinsonism, like multiple system atrophy (MSA) or progressive supranuclear gaze palsy (PSP) develop these features in early disease stages. The reduced mobility and increased time spent in sitting or lying posture leads to loss of physical independence and increased mortality. Since MSA and PSP can currently only be treated symptomatically, a long lasting independence and mobility is therefore of great importance. A positive effect has already been shown in a few studies on specific physiotherapy in patients with idiopathic Parkinson's disease (IPD), and some small studies also give us an evidence that physiotherapy in atypical parkinsonism can improve mobility. The Mobility_APP study examines the effect of two types of physiotherapy in patients with MSA, PSP and IPD. The participants are initially assigned to a type of therapy and they learn specific exercises with a physiotherapist every day for two weeks. These exercises will then be continued independently at home for another five weeks. Regular checks in the study center ensure a precise examination of the physical condition, quality of life and gait pattern. The latter will be objectively analyzed with the help of sensors that are worn on the participant's shoes. In addition, before the start and at the end of the study, the participants are also monitored for one week at home using shoe sensors in order to reflect the natural conditions of the patients. During the entire study, neither the participant nor the study investigator knows what type of therapy is being used in order to guarantee an unbiased analysis (double blinding). The aim of this double-blind, randomized-controlled study is to determine effective physiotherapy in patients with atypical parkinsonian syndromes in order to maintain mobility for as long as possible. If the exercises learned during physiotherapy can be continued regularly at home and can improve mobility, this means a big step towards autonomous therapy. Frequent visits to therapists can be reduced and sufficient and effective independent therapy can still be carried out during times of crisis or phases with increased motor impairment. The project is kindly supported by the Fund for the Promotion of Scientific Research (FWF). Together with the German Research Foundation (DFG) and Swiss National Science Foundation (SNF) in Switzerland this project can be carried out internationally in cooperation with renowned centers for neurological and sensor-based research.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple System Atrophy, Parkinson Variant (Disorder), Parkinson Disease, Progressive Supranuclear Palsy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
180 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Physiotherapy 1
Arm Type
Active Comparator
Arm Title
Physiotherapy 2
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Physiotherapy
Intervention Description
Patients will be randomized in either physiotherapy 1 or physiotherapy 2. Physiotherapy programs are individually tailored based on a structured standardized series. In order to not unblind potential participants, detailed description of both interventions will be provided after recruitment has been finished.
Primary Outcome Measure Information:
Title
Sensor-based analysis
Description
To investigate whether Physiotherapy 1 versus Physiotherapy 2 and home-based exercise lead to significantly greater improvement of lab and home-based gait parameters (gait velocity, stride length, stride time, swing time, stance time, heel strike angle and maximal toe clearance measures will be aggregated to one report value) in patients with PD, MSA-P and PSP-RS.
Time Frame
Screening/Baseline to week 7
Secondary Outcome Measure Information:
Title
Clinical Rating scales
Description
To evaluate the effects of Physiotherapy 1 versus Physiotherapy 2 on motor symptoms and on different domains of patients with MSA-P, PD, and PSP-RS by means of the patients ́ questionnaires (MoCA, Frontal Assessment Battery, International Physical Activity Questionnaire, Orthostatic Hypotension Questionnaire, 8-Item Parkinson's Disease Questionnaire, Freezing of Gait Questionnaire, System Usability Scale, Berg Balance Scale, Clinical Global Impression of severity/change, Participants Global Impression of severity/change) and clinical rating scales (MDS-UPDRS, UMSARS, PSP-RS, Hoehn & Yahr).
Time Frame
Screening/Baseline to week 7

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The subject is willing and able to give written informed consent The patient is able to tolerate all study visits including daily physiotherapy and home training. Patients similar with regard to age and sex with probable/possible MSA-P according to rev. Gilman criteria OR probable/possible PSP-RS according to MDS-PSP criteria OR PD according to MDS-PD criteria. Stable antiparkinsonian and Anti-OH medication 4 weeks prior to study entry. Exclusion Criteria: Co-morbidities that influence the clinical presentation of parkinsonian symptoms (as judged by the enrolling investigator). Participation in other clinical trials that might influence the impact of the trial intervention (as judged by the enrolling investigator) H&Y Staging score greater than or equal to 4 Change of antiparkinsonian and anti-OH medication 4 weeks prior to the interventional trial. Secondary cause of autonomic failure or parkinsonism (e.g. diabetic autonomic neuropathy, bladder surgery, drug-induced or vascular parkinsonism, etc.) Dementia according to DSM-V.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gregor Wenning, MD
Phone
+4351250481811
Email
gregor.wenning@i-med.ac.at
Facility Information:
Facility Name
Medical University Innsbruck
City
Innsbruck
State/Province
Tirol
ZIP/Postal Code
6020
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gregor Wenning, Prof
Phone
+43 50 504 81811
Email
gregor.wenning@tirol-kliniken.at
First Name & Middle Initial & Last Name & Degree
Cecilia Raccagni, MD
Email
cecilia.raccagni@tirol-kliniken.at

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Mobility in Atypical Parkinsonism: a Trial of Physiotherapy

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