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Virtual Exercises in Patients With Parkinson's Disease.

EFFECTIVENESS OF VIRTUAL EXERCISES ON THE FUNCTIONAL EXERCISE CAPACITY, FATIGUE AND QUALITY OF LIFE IN PATIENTS WITH PARKINSON'S DISEASE: A RANDOMIZED CLINICAL TRIAL

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02023034
Enrollment
20
Registered
2013-12-30
Start date
2013-02-28
Completion date
2014-02-28
Last updated
2019-08-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson Disease

Keywords

Parkinson disease, Physical Therapy, Fatigue, Quality of Life

Brief summary

Introduction: Although the motor changes are well determined in Parkinson's disease (PD), few studies describe the effects the virtual exercises on the clinical and functional outcomes in this disease. Objectives: To analyze the effectiveness of virtual exercises on functional exercise capacity, fatigue and quality of life in patients with PD. Methods: 20 subjects, 60 years old will be included, who will be randomized into 2 groups: group of virtual exercises associated with conventional exercises (n = 10) and control group with conventional exercise group (n = 10). The following variables are evaluated: functional exercise through walking test in 6 minutes, fatigue by the Fatigue Severity Scale and Quality of Life through Quality of Life Questionnaire-PDQ-39.

Interventions

OTHERVirtual exercises

The exercises will be performed with the Nintendo ® Wii Balance Board ® platform, and consist in: 1) Table Tilt; 2) Obstacle Course; 3) Tilt City; 4) Basic step; 5) Penguin; 6) Heading Soccer; 7) Basic Run. All patients underwent 12 sessions, twice a week for a period of 06 weeks.

Sponsors

Faculdade Evangelica do Parana
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* will be selected for the study * subjects with a clinical diagnosis of Parkinson's disease * 0-III H&Y * 40 to 80 years * both sexes * with preserved cognitive stage (Mini Mental\> 24).

Exclusion criteria

* will be excluded subjects who have some acute pain or associated diseases * such as severe or unstable heart disease * visual disturbances * using some march auxiliary device, which compromise the 6MWT and exercise protocol

Design outcomes

Primary

MeasureTime frameDescription
Improvement of functional exercise capacityThe subjects will be followed for a period of 90 days.Assessed by the 6-minute walk test (6MWT), according to the guidelines of the American Thoracic Society, which is based on the evaluation of the maximum distance traveled by the patient for six minutes, expressed in meters.

Secondary

MeasureTime frameDescription
Reduction of FatigueThe subjects will be followed for a period of 90 days.Assessed by the Fatigue Severity Scale, which consists of a questionnaire that assesses the impact of fatigue-related activities of daily living, rating ranges from 1 to 7 where 1 indicates little tired and 7, very tired.

Other

MeasureTime frameDescription
Improvement of Quality of lifeThe subjects will be followed for a period of 90 days.Assessed by the specific questionnaire for Parkinson's Disease, the PDQ 39.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026