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Cross-Education in People with Parkinson’s Disease, a Short-Term Randomized Controlled Trial

Not Applicable
Conditions
Parkinson's Disease
C10.228.140.079.862.500
Registration Number
RBR-64fx6x
Lead Sponsor
niversidade de Brasília
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Data analysis completed
Sex
Not specified
Target Recruitment
Not specified
Inclusion Criteria

Clinical diagnosis of PD by neurologist or physician according to the United Kingdom Parkinson's Disease Society Brain Bank criteria;
Modified Hoehn and Yahr Scale classification between stages 1 and 3;
No cognitive impairment as assessed by the Mini Mental State Examination (MMSE). The cut-off points for inclusion were > 24 points for literate individuals and > 19 for non-literate individuals;
Controlled hypertension (<150/90 mmHg);
Do not have extreme obesity (>40 Kg/m2);
Do not have a heart pacemaker;
Do not have amputation of upper or lower limbs;
Male and female volunteers from the Federal District;
Individuals between 40 and 80 years who do not have health problems and / or disabilities that prevent them from completing the test batteries and training program or who may have their problems aggravated due to participation in the program;
Availability to participate on activities proposed by researcher;
Have not practiced vigorous exercise at least 6 months previous.

Exclusion Criteria

Any kind of trauma that prevents participation in the study;
Inability to perform any of the tests that are part of the research study;
Individuals who may voluntarily want to stop their participation in research;
Individuals who do not have availability to participate in the research activities.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement of the most affected side by the disease, after the intervention, verified by following tests, dynamometer for handgrip strength, isokinetic dynamometer for quadriceps strength, Nine-Hole Peg, Box and Block, from the observation of a variation of at least 5% in the pre- and post-intervention measurements.
Secondary Outcome Measures
NameTimeMethod
Improvement of the asymmetry of the unilateral group when compared to the bilateral group, using the following equation:<br><br>Asymmetry equation = (((MA – lA)/(MA + lA)))×100<br>MA = most affected side<br>lA = less affected side<br><br>From the observation of a variation of at least 5% in the pre- and post-intervention measurements.
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