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Corticobasal Syndrome clinical trials

View clinical trials related to Corticobasal Syndrome.

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NCT ID: NCT05653778 Recruiting - Pain, Neuropathic Clinical Trials

Scrambler Therapy for Corticobasal Syndrome-Associated Pain

ST-CBS
Start date: April 5, 2024
Phase: N/A
Study type: Interventional

The goal of this pilot trial is to test whether scrambler therapy (ST) is an effective treatment for neuropathic pain in patients with corticobasal syndrome (CBS). The main question it aims to answer is: Will ST reduce pain scores by at least 33% at one month in this pilot trial, justifying further multi-center trials? Participants will: - be randomly assigned treatment from either transcutaneous electrical nerve stimulation (TENS) or ST for pain initially (eventually all patients will receive ST). - have superficial electrocardiogram (ECG) electrodes placed on the dermatomes involved with pain - obtain treatment lasting 30-40 minutes or until pain relief is obtained Researchers will compare patient's response to pain relief with TENS and ST to determine if ST is an effective treatment for central neuropathic pain.

NCT ID: NCT05073471 Recruiting - Clinical trials for Upper Extremity Dysfunction

Music and Brain Stimulation for Upper Extremity Performance in Patients With Corticobasal Syndrome

Start date: April 22, 2022
Phase: N/A
Study type: Interventional

This study is designed to investigate how musical patterns (e.g., patterned sensory enhancement, PSE) and non-invasive brain stimulation (e.g., transcranial direct current stimulation, tDCS) are effective to improve functional upper extremity performances in patients with corticobasal syndrome (CBS). 20 individuals with CBS will be randomly assigned to either PSE group (n= 10) or PSE+tDCS (n=10) group. Both interventions are 30 minutes long, twice a week for three weeks (a total of 6 sessions). Participants' self-reported and measurable outcomes including upper extremity function, kinematic quantities, quality of life, mood, cognitive level, and brain activity (e.g. electroencephalography, EEG) will be assessed in the baseline, pre- and post- each session, and follow-up phase. This study seeks to assess the possibility that music-based intervention and non-invasive brain stimulation may improve outcomes in CBS patients for patients' non-invasive but cost-effective rehabilitation settings in the future.

NCT ID: NCT02964637 Recruiting - Clinical trials for Progressive Supranuclear Palsy

Diagnosing Frontotemporal Lobar Degeneration

Start date: August 2015
Phase:
Study type: Observational

To establish diagnostic tools to make an accurate clinical and pathological diagnosis of patients with clinical FTLD syndromes