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.
Age range
18 Years – 90 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
body height using Tanita BC-418 MA device
Timeframe: through study completion, an average of 1 year
biomechanical and viscoelastic properties of the skin using MyotonPRO
Timeframe: through study completion, an average of 1 year
postural stability using the stabilometric platform Koordynacja
Timeframe: through study completion, an average of 1 year
upper limb reaction time using the Witty SEM Microgate device
Timeframe: through study completion, an average of 1 year
assessment of right and left limb compression strength (hand dynamometer)
Timeframe: through study completion, an average of 1 year
lower limb reaction time using the Balance Toutor MedTouch platform
Timeframe: through study completion, an average of 1 year
tDCS stimulation
Timeframe: through study completion, an average of 1 year
tapping test, reflex Flop test, Nine-Hole-Peg Test
Timeframe: through study completion, an average of 1 year
questionnaire Rolland-Morris
Timeframe: through study completion, an average of 1 year
Barthel scale
Timeframe: through study completion, an average of 1 year
ASIS scale
Timeframe: through study completion, an average of 1 year
Oswestry questionnaire
Timeframe: through study completion, an average of 1 year
Neck Disability Index questionnaire
Timeframe: through study completion, an average of 1 year
Sexual Satisfaction Scale for Women questionnaire
Timeframe: through study completion, an average of 1 year
Female Sexual Function Index questionnaire
Timeframe: through study completion, an average of 1 year
IEF-5 male sex life assessment questionnaire
Timeframe: through study completion, an average of 1 year
Katz scale (ADL - Activities of Daily Living)
Timeframe: through study completion, an average of 1 year
Lawton scale - IADL (basic activities of daily living)
Timeframe: through study completion, an average of 1 year
WHOQOL-BREF questionnaire
Timeframe: through study completion, an average of 1 year
Insomnia Severity Index
Timeframe: through study completion, an average of 1 year
body weight using Tanita BC-418 MA device
Timeframe: through study completion, an average of 1 year