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Taking people in PolandNo phase

Tests brain stimulation for pain and limb function in several conditions

Tests tDCS brain stimulation in adults with stroke, spinal, nerve or gynaecological pain.

Plain-language title generated from the registry record
Registry title: Use of tDCS Stimulation in Neurological and Gynaecological Conditions

Key facts

Where
Poznan, PolandSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 90 years old?

Source: NCT06891690, who can take part

Where in Poland

  • 1Department of Physiotherapy, Poznan University of Physical Education, Faculty of Sport Sciences in Gorzow Wlkp., 61-871 PoznanPoznan, PolandTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Poznan University of Physical Education
Trial code
NCT06891690
Record updated
24 September 2026
Original description
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.Read full original descriptionShow less

Use of tDCS Stimulation in Neurological and Gynaecological Conditions

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.

Inclusion: impairment of upper and lower limb function; women with selected gynaecological conditions (endometriosis, painful menstruation, dyspareunia, polycystic ovary syndrome) with no treatment other than tDCS stimulation.

Exclusion: no written consent to participate in the study; Gynaecological patients; no written consent to participate in the study.

Neurological patients.

ClinicalTrials.gov NCT06891690