NCT06891690 Use of TDCS Stimulation in Neurological and Gynaecological Conditions
| NCT ID | NCT06891690 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Poznan University of Physical Education |
| Condition | Stroke |
| Study Type | INTERVENTIONAL |
| Enrollment | 300 participants |
| Start Date | 2025-02-05 |
| Primary Completion | 2025-12-31 |
Trial Parameters
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Brief Summary
The aim of the study is to test the effect of tDCS stimulation on upper and lower limb function in neurological patients and to reduce pain in gynaecological patients. And the impact of tDCS stimulation on patients' quality of life. Standardised questionnaires will be used for pre- and post-stimulation evaluation.
Eligibility Criteria
Neurological patients Inclusion Criteria: * impairment of upper and lower limb function. Exclusion Criteria: * no written consent to participate in the study. Gynaecological patients Inclusion Criteria: * women with selected gynaecological conditions (endometriosis, painful menstruation, dyspareunia, polycystic ovary syndrome) with no treatment other than tDCS stimulation. Exclusion Criteria: * no written consent to participate in the study.
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