BEATPARK 2: Proof of Concept BeatPark

Sponsor
University Hospital, Montpellier (Other)
Overall Status
Terminated
CT.gov ID
NCT02647242
Collaborator
Université Montpellier (Other), University Ghent (Other), Tecnalia (Other), National University of Ireland, Maynooth (Other)
45
1
8.4

Study Details

Study Description

Brief Summary

Physical activity has demonstrated its beneficial effect on functional capabilities and quality of life in patients with PD. However, the daily physical activity remains limited in these patients. Rhythmic auditory cueing improves spatio-temporal gait parameters in patients with PD. The first results of BeatHealth studies have allowed us to identify the best musical stimulation to improve these parameters and the motivation of the patients.

The originality of this study is to propose a gait auto-rehabilitation program using BeatHealth device with optimal auditory cueing during four weeks in ecological conditions in PD.

Observance (utilization's time), safety (falls, pain, fatigability) and efficacy (gait parameters, balance, quality of life) will be evaluated.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Auto rehabilitation program of gait with Beat Health device.
N/A

Detailed Description

Objectives Main goal: To evaluate the observance of the use of BeatHealth device in gait auto-rehabilitation program in patients with PD.

Secondary objectives :
  1. To evaluate safety by the number of falls

  2. To evaluate tolerance by the evaluation of pain and fatigue

  3. To evaluate the expected improvement on gate and quality of life essentialy

  4. To identify predictive factors associated with a good response to the program

  5. To evaluate the technical feasibility.

Methods Design : prospective and descriptive study Population : 60 patients with PD Inclusion criteria : PD diagnosed according the international criteria form the United Kingdom Parkinson's Disease Society Brain Bank ; gait disorder identified by the neurologist or the rehabilitation doktor ; to be able to work 30 minutes consecutively and without technical support Non inclusion criteria : signs for atypical parkinsonism

Main evaluation criteria:

Percentage of time of use of the BeatHealth device compared to the prescribed schedule (30 minutes of walk, 5 times a week during four weeks : 10 hours for the complete study) .

Secondary evaluation criteria :

n°1 - Auto-evalation of the number of falls reported by the patient on a daily agenda before and during the rehabilitation program.

n°2 - Auto-evalation of pain with a visual analogic scale on a daily agenda before and during the rehabilitation program.

n°3 - (a) gait functional capabilities; (b) spatio-temporal parameters of gait; (c) motot severity of the disease(d) balance ; (e) quality of life ; (f) psychopathological evaluations (g) auditory-sensori-motor and timing capabilities (h) sleep.

n°4 - Numbers of correct connections to the program, number of errors of manipulations, number of phone calls for help.

Statistical analysis : In the randomized control study on 21 patients from Martin et al. (2015) evaluating a rehabilitation programm on rythmic auditory cueing by metronome in patients with PD wiht fall potential, program observance was 83% according to self evaluation by the patients. In our study , to estimate this percentage of about 80% with an accuracy of ± 10% (interval of 20%) with a confidance interval of 95, the number of subjects to include is 60.

Main statistical analysis : in order to evaluate the observance of the BeatHealth device, the percentage of the time of use conpared to the prescribed time (10 hours in total)

Program schedule :

Number of visits : 3 Inclusion period : 7 months Follow-up : 2 weeks (from the inclusion to the beginning of the program) + 4 weeks (program) Calendar of the study : january 2016 - october 2016

Content of the visites :

V0=Inclusion / identification of the favorite musical genres of the patient / Explanation and delivery of the agenda.

V1=

  • Evalutation criteria

  • Information and training to the BeatHealth device use (sensors, smartphone use, connexion to the cloud for the transfer of the results)

  • Operating instructions delivery

  • Explanation of the rehabilitation program (number of sessions, duration, place…)

  • Communication of the contact details of the maintenance operator V2= identical to V1 (except for predictive factors).

Description of the intervention The auto-rehabilitation program will consist in an outside walk, during 5 sessions of 30 minutes per week during 4 weeks with the beatHealth device, delivering the optimal rythmic auditory cueing. The device will associate an Android smartphone, hold at the belt, connected by bluetooth to a headphone and to two sensors strapped to the ankles. The patient will transfer the data collected by BeatHealth to a secured website and will complete the agenda

Study Design

Study Type:
Interventional
Actual Enrollment :
45 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Pilot Study on Feasibility and Safety of a Gait Auto-rehabilitation Program by Rhythmic Auditory Cueing Delivered by BeatHealth in Patients With Parkinson's Disease.
Actual Study Start Date :
Nov 24, 2015
Actual Primary Completion Date :
Aug 5, 2016
Actual Study Completion Date :
Aug 5, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients with parkinson's disease

Patients with parkinson's disease

Behavioral: Auto rehabilitation program of gait with Beat Health device.
The auto-rehabilitation program will consist in an outside walk, during 5 sessions of 30 minutes per week during 4 weeks with the beatHealth device, delivering the optimal rythmic auditory cueing. The device will associate an Android smartphone, hold at the belt, connected by bluetooth to a headphone and to two sensors strapped to the ankles. The patient will transfer the data collected by BeatHealth to a secured website and will complete the agenda

Outcome Measures

Primary Outcome Measures

  1. Percentage of time of use of the BeatHealth device compared to the prescribed schedule [4 weeks]

    measured automatically by Beathealth device

Secondary Outcome Measures

  1. Auto-evalation of the number of falls reported by the patient on a daily agenda [4 weeks]

    self reported in a diary

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Idiopathic Parkinson's Disease confirmed by the United Kingdom Parkinson's Disease Society Brain Bank's criteria (Gibb and Lees, 1988; Hughes et al., 1992)

  • Gait disorder confirmed by a neurologist

  • Ability to walk more than 30 minutes without any device as a stick or a walker

  • Stability of the dopaminergic treatment

Exclusion Criteria:
  • Pregnancy

  • Hearing problems

  • Other neurological disease affecting gait other than PD

  • Other gait disorder whetever the etiology (orthopedic, rheumatologic….)

  • Uncompensated heart or respiratory failure excluding possibility of intensiv rehabilitation.

  • Arguments for atypical parkinsonism

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University Hospital, Montpellier
  • Université Montpellier
  • University Ghent
  • Tecnalia
  • National University of Ireland, Maynooth

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University Hospital, Montpellier
ClinicalTrials.gov Identifier:
NCT02647242
Other Study ID Numbers:
  • UF 9193-4
First Posted:
Jan 6, 2016
Last Update Posted:
Dec 29, 2021
Last Verified:
Dec 1, 2021
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 29, 2021