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NCT06856941Recruiting

CsDCS on Functional Mobility in Parkinsons Disease

Cerebello-spinal Direct Current Stimulation Associated with Treadmill Gait Training in Functional Mobility in Patients with Parkinsons Disease

Source: ClinicalTrials.gov · Last updated 4 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Parkinsons disease is a progressive neurological disorder marked by a decline in the efficacy of dopaminergic synapses in the nigrostriatal pathway, causing motor disturbances. Resting tremor, bradykinesia, and muscle rigidity are the most prominent motor features. These factors result in gait impairments, including slowness and freezing. The primary treatment for the disease is medication. However, while medication does reduce motor symptoms, prolonged usage may lead to an increase of dyskinesias and a worsening of a patients clinical condition. Thus, alternative therapies, such as cerebellospinal direct current stimulation (csDCS), have gained popularity. Studies suggest that csDCS may be an effective approach to mitigate gait disorders in this patient population. Kinesiotherapy is an established therapeutic method that has been demonstrated to promote functional mobility and improve gait. To date, the combination of kinesiotherapy and csDCS has not been tested, thus the purpose of this study is to evaluate the effectiveness of this combined therapy for enhancing functional mobility in Parkinsons disease patients. The goal of this study is to assess the efficacy of blending csDCS and kinesiotherapy for improving patients functional mobility in Parkinsons disease. Two groups of volunteers will be assigned: i) actual csDCS + kinesiotherapy, and ii) sham csDCS + kinesiotherapy. The full procedure involves 10 therapy sessions conducted across two weeks.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
66 (estimated)
First submitted
26 Feb 2025
Start date
9 May 2024
Primary completion date
Jul 2025
Lead sponsor
Universidade Federal de Pernambuco
NCT number
NCT06856941

What you commit to

  • Study type: Interventional
  • Planned participants: 66
  • From 9 May 2024 to the primary completion date, Jul 2025
  • 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.

Prior treatment

  • have undergone previous surgery for PD

Other illness

  • other neurological disorders, postural hypotension, vestibular, musculoskeletal or visual disorders that compromise performance in the proposed tests
  • other osteoarticular diseases in the lower limbs that interfere with performance and locomotion

Other

  • a Montreal Cognitive Assessment (MoCA) score of less than 21 points

Who the study is looking for

  • a clinical diagnosis of PD provided by a neurologist
  • regular dopaminergic drug treatment (at least three months of use)
  • aged 40 years or over
  • staging I to IV on the modified Hoehn and Yahr scale

Age in the registry: 40 years to - · 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
Universidade Federal de Pernambuco
Coordinator of this site? Confirm its status
RecifeBrazilRecruiting

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