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Evaluation of rehabilitation effect on balance, sleep quality, life quality and fatigue in Parkinson disease patients.

Not Applicable
Conditions
Parkinson.
Parkinson disease, Incl: Hemiparkinsonism, Paralysis agitans Parkinsonism or Parkinson disease: NOS, idiopathic, primary
Registration Number
IRCT2015070123012N1
Lead Sponsor
Vice chancellor for research,Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

All of the patients should be in stage 2 or 3 of Parkinson disease based on Hoehn and Yahr criteria and also should: be under stable pharmacological treatment regime at least 30 days before entrance in study; be in stable clinical condition to complete the study; have appropriate primary response to Levo-DOPA or it's agonist; not have Parkinson related dementia; not have abnormal MRI; not have drug related parkinsonism.
Exclusion criteria: patient unwillingness to complete the study; patient inability to complete the study because of any reason at any time during the study.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Balance. Timepoint: Before, just after 8 sessions of trans cranial direct current stimulation plus occupational therapy and 3 months later. Method of measurement: Berge-Balance questionnare.;Sleep quality. Timepoint: Before, just after 8 sessions of trans cranial direct current stimulation plus occupational therapy and 3 months later. Method of measurement: Epworth questionnaire.;Life quality. Timepoint: Before, just after 8 sessions of trans cranial direct current stimulation plus occupational therapy and 3 months later. Method of measurement: EQ-D5 questionnaire.;Tiredness. Timepoint: Before, just after 8 sessions of trans cranial direct current stimulation plus occupational therapy and 3 months later. Method of measurement: Fatigue severity scale questionnaire.
Secondary Outcome Measures
NameTimeMethod
Side effects. Timepoint: During and just after each session of trans cranial direct current stimulation performance. Method of measurement: Asking from a patient.
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