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

Effects of unilateral and bilateral training methods on motor control and strength in individuals with Parkinson's disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-64fx6x
Enrollment
Unknown
Registered
2018-12-01
Start date
2018-03-21
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Parkinson's Disease

Interventions

Resistance training with weights, one group trained unilaterally and the other group trained bilaterally. The control are themselves at the pre-intervention moment (without treatment). The trainings o
Other
I02.233.543

Sponsors

Universidade de Brasília
Lead Sponsor
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Collaborator

Eligibility

Age
40 Years to 80 Years

Inclusion criteria

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 (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

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.

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
Improvement of the asymmetry of the unilateral group when compared to the bilateral group, using the following equation: Asymmetry equation = (((MA – lA)/(MA + lA)))×100 MA = most affected side lA = less affected side From the observation of a variation of at least 5% in the pre- and post-intervention measurements.

Countries

Brazil

Contacts

Public ContactSacha Clael

Universidade de Brasília

sachaclael@hotmail.com+55061983837418

Outcome results

None listed

Source: REBEC (via WHO ICTRP)