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NCT07567599Enrolling by invitation

Deep Brain Stimulation in Parkinson's Disease: Motor and Functional Outcomes

Effects of Deep Brain Stimulation Surgery on Motor and Functional Outcomes in Individuals With Parkinson's Disease: An Uncontrolled Clinical Trial

Source: ClinicalTrials.gov · Last updated 29 Jul 2026

Brief summary (registry, in English)

Introduction: Parkinson's Disease (PD) is a progressive neurodegenerative condition characterized by classic motor symptoms, such as bradykinesia, rigidity, resting tremor, and postural instability, which directly compromise the mobility and autonomy of individuals with PD. Furthermore, non-motor manifestations, including autonomic, cognitive, and emotional changes, impact the quality of life of individuals with PD. Deep Brain Stimulation (DBS) surgery is a well-established treatment to assist in improving the primary motor symptoms of PD; however, literature is scarce in describing specific results regarding physiotherapeutic aspects, such as the motor symptoms that determine better quality of life and social participation for individuals with PD. Determining whether factors amenable to improvement prior to surgery-such as bradykinesia, muscle strength, and balance-are related to better motor and functional outcomes in individuals with PD post-DBS is of great importance to ensure a better result from the surgical intervention. Objective: To compare motor outcomes (gait speed, balance, freezing of gait, fear of falling, muscle strength, functional capacity, and physical activity level) of individuals with PD after undergoing DBS, relative to the motor status previously observed in the preoperative period. Methods: This is an uncontrolled clinical trial, with data collection conducted at the Neurovida private multidisciplinary clinic and the Hospital Santa Casa in Belo Horizonte. This study will be registered at www.clinicalTrials.gov and conducted according to the Consolidated Standards of Reporting Trials (CONSORT) recommendations. The present study will be submitted to the Research Ethics Committee of the Federal University of Minas Gerais (COEP) and will only commence after proper approval. All necessary consents for the development of the study have been obtained. The sample consists of individuals with idiopathic PD selected by a clinical neurologist specializing in movement disorders. The inclusion criteria for the present study are: having idiopathic PD diagnosed for more than five years, being under treatment with a neurologist specializing in movement disorders, and having an indication for DBS. Descriptive statistics and normality tests will be performed for all study variables. Selected variables will be compared in terms of mean difference between post- and pre-surgery measurements, considering a 95% CI. In all analyses, a significance level of α=0.05 will be considered, using the SPSS statistical package version 15.0 for Windows.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
40 (estimated)
First submitted
28 Apr 2026
Start date
2 Jun 2026
Primary completion date
Feb 2027
Lead sponsor
Federal University of Minas Gerais
NCT number
NCT07567599

What you commit to

  • Study type: Interventional
  • Planned participants: 40
  • From 2 Jun 2026 to the primary completion date, Feb 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Individuals who do not wish to undergo surgery; those with severe cardiovascular or orthopedic comorbidities that pose a risk during the surgical procedure; and those presenting with dementia or severe psychiatric disorders that could be exacerbated by the surgery.

Who the study is looking for

  • Individuals with PD who have been evaluated by a clinical neurologist specializing in movement disorders and have a medical indication for DBS surgical treatment. These individuals will undergo surgical screening, which includes prior neurological, speech-language pathology, neuropsychological, and physical therapy assessments.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Clínica NeuroVida
Coordinator of this site? Confirm its status
Belo HorizonteBrazilUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.