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The effects of dance therapy on Parkinson's disease symptoms

Dance as an adjuvant therapy in the rehabilitation of patients with Parkinson's disease: clinical and methodological trials

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3bhbrb5
Enrollment
Unknown
Registered
2022-03-30
Start date
2018-02-10
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 Disease

Interventions

Experimental group: thirty people from 40 years of age, of both sexes, diagnosed with Parkinson's Disease and in physical conditions to participate in the activities proposed in the intervention, as e

Sponsors

Universidade Federal do Pará
Lead Sponsor
Universidade Federal do Pará
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Diagnosis according to the UK Parkinson's Disease Society Brain Bank; Hoehn and Yahr stage I to III; under pharmacological treatment for at least 3 years; and in physical conditions to perform the dance intervention.

Exclusion criteria

Exclusion criteria: People without physical conditions to perform the tests and dance intervention; who have other neurological or neuropsychiatric conditions; or have serious comorbidities that may pose a risk for the practice of physical activities.

Design outcomes

Primary

MeasureTime frame
Expected outcome 1. Improvement of motor and balance functions, assessed by the Timed Up-and-Go Test (TUG) (Greene et al. 2010), Performance Oriented Balance Assessment (POMA) (Faber et al. 2006) and the Berg Balance Scale (BBS) (Kornetti et al. 2004) associated with the use of accelerometry protocols. The improvements are expected to be inside the clinically meaningful results observed for aged people which range in between 6 and 10% of motor improvements in several scales. These results may not represent statistically significant differences, but on the clinical scenario they improve meaningfully the quality of life and performance on daily activities of patients, especially regarding a incurable and progressive degenerative disease.

Secondary

MeasureTime frame
Expected outcome 2. Improvement of cognitive functions, assessed by the "Frontal Assessment Battery - FAB" (Dubois et al. 2000) and the "mental rotation test" (Mental Rotation Task - MRT) (Hegarty 2018). For these tests, significant improvements on the whole score calculated by t test between scores before and after intervention, on the whole test or in any of its subdivisions, considering a confidence interval of 95% will be considered relevant.;Expected outcome 3. Improvement of neuropsychiatric effects as assessed by the apathy scale (AS) (Marin et al. 1991) and the Montgomery and Asberg depression scale (MADRS) (Snaith et al. 1986). For apathy Scale the results range between 0 and 42, with a score of 14 considered indicative of clinically meaningful apathy, therefore reductions beyond this range will differentiate between the presence of the condition and its absence, For MADRS scale we will consider the reduction among 10% to be relevant.;Expected outcome 3. Improvement of biochemical changes associated with Parkinson Disease through blood collection, especially the interleucins related to the infammatory responses (e.g. IL-4 and 6) which is well described to be involved in neural cell death mechanisms in several neuropathologic conditions. We expect that the interleucins levels will be altered in al patients, and the outcome of the intervention according to our hypothesis should bring them closer to the normal ranges described in the literature. Changes around 5% of the difference between the normal and the observed initial range will be considered as relevant.

Countries

Brazil

Contacts

Public ContactJuliana Duarte

Universidade Federal do Pará

julianadsantosduarte@gmail.com+55 91996254382

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 10, 2026