About this trial
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
This trial accepts healthy volunteersQualifiers
impairment of upper and lower limb function.
Disqualifiers
no written consent to participate in the study.
women with selected gynaecological conditions (endometriosis, painful menstruation, dyspareunia, polycystic ovary syndrome) with no treatment other than tDCS stimulation.
no written consent to participate in the study.
Trial design
Single group
Treatments tested in this trial
tDSC stimulation
Other interventiontDCA stimulation not exceeding 2 mA
Treatment groups
Trial outcomes
Primary outcomes
body height using Tanita BC-418 MA device
height will be measured in centimeters
biomechanical and viscoelastic properties of the skin using MyotonPRO
The tissue voltage will be measured in Hertz (Hz)
postural stability using the stabilometric platform Koordynacja
the lower the frequency of anterior-posterior and medial-lateral swings, the better the stability
upper limb reaction time using the Witty SEM Microgate device
the shorter the time in seconds measured with a stopwatch, the better the result,
Sponsors and contacts
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