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Clinical Trials/NCT04580849
NCT04580849
Completed
Not Applicable

Telerehabilitation Using a Dance Intervention in People With Parkinson's Disease

Federal University of Health Science of Porto Alegre1 site in 1 country24 target enrollmentSeptember 5, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
Federal University of Health Science of Porto Alegre
Enrollment
24
Locations
1
Primary Endpoint
feasibility (adherence rates)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

The aim of this study is to verify the feasibility of a telerehabilitation approach with dance in people with parkinson's disease.

Detailed Description

This is a feasibility study that aims to investigate the safety and efficacy of dance classes via an online platform in people with and without Parkinson's Disease. The intervention will last 2 months and the classes will be conducted twice a week (60 minutes) using the Zoom platform. Evaluations will be performed before and after the intervention by means of the Zoom platform as well and will include questionnaires of quality of life, depression, anxiety, and activities of daily living.

Registry
clinicaltrials.gov
Start Date
September 5, 2020
End Date
December 5, 2020
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Federal University of Health Science of Porto Alegre
Responsible Party
Principal Investigator
Principal Investigator

Aline de Souza Pagnussat

Principal Investigator

Federal University of Health Science of Porto Alegre

Eligibility Criteria

Inclusion Criteria

  • Individuals with and without parkinson's disease according London Brain Bank Criteria
  • Minimal cognitive ability to understand commands (MMSE)
  • Able to stand at least 10 minutes with or without support
  • Dopamine medication stable at least 6 weeks before the beginning of the study
  • Portable device and internet connection

Exclusion Criteria

  • Severe visual or auditive disturbances
  • Neurological disease (other than parkinson's for those included) or severe neuromuscular disorders that prejudice the proposed activities

Outcomes

Primary Outcomes

feasibility (adherence rates)

Time Frame: 10 weeks

To assess the feasibility of the study design and procedures. The adherence rate will be calculated by the total number of patients who completed the full course of intervention divided by the total number of patients included at the beginning.

Secondary Outcomes

  • feasibility (patients opinions)(10 weeks)
  • 36-Item Short Form Survey (SF-36)(Change from Pre to Post treatment (10 weeks))
  • Hospital Anxiety and Depression Scale (HADS)(Change from Pre to Post treatment (10 weeks))
  • Parkinson's Disease Questionnaire-8 (PDQ-8)(Change from Pre to Post treatment (10 weeks))
  • Unified Parkinson's Disease Rating Scale (UPDRS) Part I(Change from Pre to Post treatment (10 weeks))
  • Activities-Specific Balance (ABC) Scale(Change from Pre to Post treatment (10 weeks))
  • feasibility (safety and usability)(10 weeks)
  • Five Times Sit to Stand Test (FTSTS)(Change from Pre to Post treatment (10 weeks))

Study Sites (1)

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