Skip to main content
Clinical Trials/NCT03212014
NCT03212014UnknownNot Applicable

Development and Research of an Individualized Intelligent Platform for Rehabilitaion in Patients With Parkinson's Disease

Taipei Veterans General Hospital, Taiwan1 site in 1 country75 target enrollmentStarted: January 1, 2017Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
75
Locations
1
Primary Endpoint
mini-BESTest

Study Overview

Brief Summary

The present study aims to compare the clinical efficacy of intelligent POWER therapy, intelligent LSVT-BIG therapy, and the three exercise models currently in clinical use. DCM_IR analysis will also be incorporated into the analysis to develop a personalized and intelligent Parkinson's rehabilitative therapy platform.

Detailed Description

Background:

Parkinson's disease is a progressively degenerative disorder. Patients need early screening, therapeutic intervention, and personalized interaction with outpatient rehabilitative treatment. In the past, it had been difficult to meet these goals. Recent advances in bio-sensors technology has enabled collection of bio-metric data. Models of brainwave analysis have also matured. In addition, our ability to analyze vibrational spectrogram had also greatly improved. How to combine these enabling technologies to meet the needs of Parkinson's patients is an urgent topic of research.

Objective:

The present study aims to compare the clinical efficacy of intelligent POWER therapy, intelligent LSVT-BIG therapy, and the three exercise models currently in clinical use. DCM_IR analysis will also be incorporated into the analysis to develop a personalized and intelligent Parkinson's rehabilitative therapy platform.

Method:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
40 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •.Parkinson's disease diagnosis, Hoehn-Yahr level I-III
  • •.Stable medicine intake for 2 weeks at least
  • •.Able to walk independently for 15 meters
  • •.Aged 40-85 years old

Exclusion Criteria

  • •.Cognition deficits(MMSE score<24)
  • •.Combined other neurological disease, such as stork, SCI, and so on.
  • •.Pregnant or Breastfeeding

Arms & Interventions

LSVT-BIG

Experimental

Participants in this group would be treated with LSVT-BIG for three months

Intervention: LSVT-BIG (Other)

POWER

Experimental

Participants in this group would be treated with POWER for three months

Intervention: POWER (Other)

Traditional rehabilitation

Active Comparator

Participants in this group would be treated with traditional exercise rehabilitation for three months

Intervention: Traditional rehabilitation (Other)

Outcomes

Primary Outcomes

mini-BESTest

Time Frame: 15 mins

Mini BESTest assesses dynamic balance, a unidimensinal construct and includes 14 items addressing 4 of the 6 sections of the original BESTest (anticipatory postural adjustments, reactive postural control, sensory orientation, dynamic gait).

Secondary Outcomes

  • Unified Parkinson's disease rating scale(15 mins)
  • muscle power of lower extremity(5 mins)
  • PDQ-39(30 mins)

Investigators

Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials

Development and Research of an... | Clinical Trial