Parkinson Disease Clinical Trial
Official title:
Parkinson App SmarTphone Aimed to Improve Walking Ability and Reduce Fall (P.A.S.T.A.)
Gait impairments of patients with Parkinson's disease (PD) limit the independence in the daily activities and sensibly increase the risk of falls. New gait analysis methods, based on wearable inertial sensors, have been proposed to track the gait features during treatment and in real-life conditions. Gait training based on auditory cues as Rhythmical Auditory Stimulation (RAS) have preliminarily shown positive effects improving gait velocity, stride length, step cadence of walking in PD. In the current project, the research group will aim to develop a smartphone application (Parkinson App Smartphone Aimed: P.A.St.A.) integrated with sensors and RAS. In a second time, investigators will analyze the spatio-temporal gait parameters obtained by the wearable sensors and the sociodemographic and clinical data, thus generating a big data set, to improve the knowledge about current pharmacological therapies and rehabilitation.
Parkinson's disease (PD) is a chronic and progressive movement disorder, mainly due to an
altered motor control. Gait impairments are the primary symptoms in patients with PD, with a
decreased step length and walking speed, abnormal gait phases distribution, inconstant pace,
gait asymmetry and reduced joint coordination. The postural instability and the deterioration
of the gait features sensibly increase the risk of falls in these patients, resulting in loss
of independence and a worsening of long-term prognosis. It has been clearly demonstrated that
motor impairments are connected to a dysfunction of basal ganglia, a brain structure that
works as a "pacemaker" for the activation (and deactivation) of each sub-movement within a
repetitive movement sequence. Disruption of internal rhythmic cues in PD may explain the poor
smoothness of the movement execution and the difficulties in regulating stride length,
resulting in a cadence increase. Levodopa therapy is the most effective treatment to improve
the symptoms in PD, but a long-term administration reduces its efficiency over time and it is
responsible for collateral effects (dyskinesia). Hence, researches have investigated
alternative non-pharmacological approaches, based on auditory cues as the Rhythmical Auditory
Stimulation (RAS). A large number of studies have reported positive effects both after a
single session of treatment and after longer training programs, with improved gait velocity,
cadence, and stride length as well as in the symmetry of muscle activation for upper and
lower extremities. In such studies, RAS frequencies are pre-set as percentages of the
patient's preferred walking frequency. Because the duration of all the therapies may change
over time, it is necessary a continuous adjustment of the dosage and type of treatment, based
both on patients' monitoring of the symptoms and on objective evaluations. Gait analysis (GA)
methods have been proposed and validated for the study of physiologic gait and in several
diseases. The traditional systems of GA are based on optoelectronic systems, but they are
expensive, not portable and requiring skilled operators. The assessment is always performed
in laboratories with experimental set-ups, likely different from real-life walking (noise
environments, presence of objects and people or unlevelled pavement, different colors).
Consequently, traditional GA is not reliable for the daily control of the treatments or for
the assessment of the real-life situations. Recently, researchers have developed wearable
systems, based on Inertial Measurement Units (IMUs). Even if a considerable number of studies
have explored the validity of IMUs analysis, very few have been involved in PD motion
analyses. During the last few years, a set of wearable devices embedding inertial sensors,
are spread on the market as low-cost solutions for monitoring human motion activities. While,
they still have to be fully validated in accuracy, these systems can provide the user
information to track his/her own activity. This persuasive technology has a terrific
potential to enhance physical activity and motivation of the patients, with the advantage of
prolonged and continuous recording.
The use and the analyses of a large amount of objective data (big data set) is the new
frontier for an efficient use of scientific time and resources, engaging the care
coordination program, saving economic resources, and providing a higher quality of care. In
addition, these systems, integrated with a web-based application, telemedicine and mobile
smartphones, could help clinicians to address more properly the treatments through a
real-time monitoring in an everyday life. Our research group has been involved in the
clinical evaluation of different aspects of gait quality in many neurological conditions, PD
included. Investigators have already shown as wearable accelerometers could be useful in the
quantitative assessment of the dynamic gait stability, in correlation with clinical scores.
Researchers have also found that accelerations could be altered in a pathology-specific
manner (intellectual disabilities performing different tasks simultaneously). A similar
condition can be observed also in PD, showing that only the intrinsic gait harmony
significantly correlate with severity of gait impairments. In the recent years, a lot of
wearable tools have become available to quantify the daily activity. This is particularly
important for possible therapeutic use of the RAS, that is addressed to restore a harmonic
pace in patients with PD.
Specific Aim 1: To analyze motor pattern in PD patients in real life setting, gait features
will be obtained by wearable sensors in order to relate them with clinical and demographical
data.
Specific Aim 2: To improve walking abilities and to reduce the risk of falls in patients with
PD, researchers will test a real-time acoustic feed-back (RAS) and alerts from integrated
sensors connected with a suitable and easy-to-use application for smartphones.
Specific Aim 3: To improve pharmacological and rehabilitative protocols, investigators will
analyze the daily life gait and motility data and the clinical features to test the
theoretical risk model of falls.
Experimental Design Aim 1: Patients with PD will be recruited at Fondazione Policlinico
Universitario Gemelli and Fondazione Don Gnocchi ONLUS in Rome. All included patients will be
affected by idiopathic PD. Clinical data will be acquired by a trained neurologist.
Three hundred patients will be remotely monitored through wearable sensors. Subjects will be
instructed to wear the sensor for 14 consecutive days. Each patient will have more than 100
measurements every second, generating a large amount of data, which will be stored in a
database and subsequently filtered for data of interest. Spatio-temporal gait parameterswill
provide information to monitor the performance of patient's walking in order to get an
accurate measure of the overall efficacy of the locomotor function. Then, they will be
integrated with the electronic patient records. Clinical data, as physician's prescriptions,
medical imaging and other administrative data will be recorded. Finally, a risk model for the
prediction of falls will be constructed.
Experimental Design Aim 2: After the analysis of the obtained data, an application will be
developed (Parkinson App Smartphone Aimed: P.A.St.A.), it will be characterized by
reliability, easy-to-use, visual clarity, and affordability.
This application will be able to: 1) record the gait features sending them to a server in the
cloud; 2) provide acoustic feedback adapted on patient's gait features (with higher or lower
frequency on the basis of the patient's needs and on the predictive risks); 3) provide alert
on the basis of risk indices (risk indices will be identified according to a risk model for
the prediction of falls) and 4) be updated whenever needed (e.g. after a fall). Fifty
patients will be provided with a smartphone, after a training on the use of the software
application developed by the team project. They will use the application for a period of 14
consecutive days. Clinical assessments with scales will be performed, pre- and post-use of
P.A.St.A., to analyze the motor function and the postural stability and, finally, the quality
of life. In addition, the compliance to the adoption of the novel technology will be
investigated.
Experimental Design Aim 3: The obtained computational data will be related with clinical
features and gait patterns to identify clinical biomarkers for gait impairment in PD. The
availability of a big data-sets, powered by the assessments of thousands of patients with PD,
will allow the improvement of knowledge on motor pattern in real life setting and to improve
the current therapeutic approach.
Metodologies and statistical analyses: All statistical analyses will be conducted using Stata
software.
AIM 1 - Data will be summarized as frequencies and percentages for categorical variables.
Continuous variables will be analyzed as means and standard deviations or medians and ranges.
Investigators will look for normality by using normal plots or by significance tests (e.g.
Shapiro-Wilk W test). The incidence of falls will be measured and the circumstances under
which they occur and their consequences will be described, categorized as no injury, minor or
major injuries. A multiple logistic regression analysis will be used to determine independent
predictors of falls. Variables will be selected for entry into the logistic model based on
the results of a univariate analyses. The Hosmer-Lemeshow goodnessof-fit test will be used to
assess how well the model accounted for specific outcomes. The prediction model for falls
will be developed from the results of the multivariate analysis. The predictive score will be
calculated by odds ratio based scoring method, and the nearest integer scores will be
assigned to each predictor. Model discriminative power will be evaluated by
receiver-operating characteristic area under the curve analysis.
AIM 2 - Data recorded will be processed to extract gait and dynamic balance parameters. The
incidence of falls, the use of RAS and its correlation to the risks indices within the 14
days of follow-up will be measured. The Wilcoxon signed-rank test will be performed to
compare the number of fall(s) before and after the use of P.A.St.A.
AIM 3 - Spatio-temporal gait parameters, and demographic and clinical characteristics of
patients before therapies, will be compared using the Chi squared test, Fisher's exact test,
and independent t-tests where appropriate.
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