NCT07534397Enrolling by invitation
Treatment of Cognitive and Sensorimotor Deficits in Parkinson's Disease With High Definition Transcranial Direct Current Stimulation
Source: ClinicalTrials.gov · Last updated 3 Nov 2026
Brief summary (registry, in English)
The purpose of this research study is to examine the effects of transcranial Direct Current Stimulation (tDCS) on verbal retrieval and cognition and sensorimotor control and to determine if tDCS can be used as a way to improve retrieval, sensory, and motor abilities in individuals with Parkinson's disease (PD).
- Status (registry)
- Enrolling by invitation
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- First submitted
- 9 Apr 2026
- Start date
- 15 Sept 2026
- Primary completion date
- 31 Oct 2027
- Lead sponsor
- The University of Texas at Dallas
- Diseases
- Parkinson disease
- NCT number
- NCT07534397
What you commit to
- Study type: Interventional
- Planned participants: 20
- From 15 Sept 2026 to the primary completion date, 31 Oct 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.
Prior treatment
- cranial implants or skull defects that affect tDCS administration;
- any electrically, magnetically, or mechanically activated implants;
- diagnosis of just dysarthria;
- Use of medications that interact with or potentially interact with tDCS or EEG effects:
Other illness
- history of seizures;
- unexplained episodes of loss of consciousness (as these may be related to brain alterations or epilepsy);
- unstable or uncontrolled neuropsychiatric illness;
- brain tumor; stroke; present drug abuse/misuse;
- serious or life-threatening diseases, including congestive heart failure, chronic obstructive pulmonary disease, or active malignancy;
- Huntington's disease;
- stroke;
- cardiac, neural, or medication implants;
- skin conditions such as dermatitis, psoriasis, or eczema;
Other
- A potentially study-confounding, tDCS-contraindicated, or EEG-contraindicated psychological, neuropsychiatric, neurological, or other medical issues:
- Montreal Cognitve Assessment (MOCA) score \<23, unless an accompanying study partner/caregiver is with them and we can obtain the written consent of both the participant and the participant's accompanying study partner/caregiver (i.e., the participant's spouse, adult child, parent, or adult sibling);
- suffering from severe or frequent headaches;
- severe traumatic brain injury (based on the Ohio State TBI Identification; Method);
- brain tumor;
- implanted brain medical devices, including, deep brain stimulators (DBS);
- implanted pacemakers;
- vascular clips or other electrically sensitive support systems in the brain;
- damaged skin at the sites of stimulation (the device should only be used on healthy, intact skin, as wounds may alter resistance to current);
- pregnant women;
- anti-convulsants;
- carbamazepine;
- sulpiride;
- pergolide;
- lorazepam;
- rivastigmine;
- dextromethorphan;
- D-cycloserine;
- flunarizine;
- ropinirole;
- citalopram;
- stimulants;
- Additionally, non-English speakers will be excluded because not all of the screening forms, questionnaires, and tests are available in languages other than English.
Who the study is looking for
- Diagnosed with PD having a verbal fluency deficit based on neuropsychological test (T-score \< 40 or a T-score \<-1.0 SD below the average T-score): Semantic Object Retrieval Test (SORT), COWAT (both letter and category fluency), Boston Naming Test (BNT), Rey Auditory Verbal Learning Test (RAVLT)
- 50 - 90 years old
- Capable of understanding and signing an informed consent (able to answer consent comprehension questions)
- Fluent in speaking and reading English
Age in the registry: 50 years to 90 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Callier Clinical Center, The University of Texas at Dallas Coordinator of this site? Confirm its status | Richardson | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.