Clinical trial Recruiting at 1 site Interventional Ages 18 to 90

Using tDCS stimulation to improve function and reduce pain in neurological and gynaecological patients

Official title: Use of tDCS Stimulation in Neurological and Gynaecological Conditions

Run by Poznan University of Physical Education · NCT06891690 · Data updated 2026-11-12

This study is testing if a brain stimulation treatment can help improve movement and reduce pain for people with neurological and gynecological conditions.

Quick facts

Study typeInterventional
Ages18 Years to 90 Years
SexAll
Enrollment300 (estimated)
SponsorPoznan University of Physical Education
Academic / other
Locations1 site (Poznan)
StatusRecruiting
StartedFebruary 5, 2025
Main results expectedSeptember 30, 2026
Study endsSeptember 30, 2026
Registry record updatedSeptember 24, 2026
Trial IDNCT06891690 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include individuals aged 20-90 with upper and lower limb impairments due to stroke, spinal cord diseases, or specific gynaecological conditions.

Probably not a fit

Patients who do not provide written consent or those with conditions not specified in the inclusion criteria may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study aims to evaluate the effects of transcranial direct current stimulation (tDCS) on upper and lower limb function in neurological patients, as well as its potential to alleviate pain in gynaecological patients. Participants will undergo a rehabilitation program that includes tDCS stimulation, with assessments conducted using standardized questionnaires before and after treatment. The study will involve individuals aged 20-90 with specific neurological and gynaecological conditions, and will compare outcomes based on the number of tDCS sessions received. The goal is to determine the effectiveness of tDCS in enhancing quality of life and functional abilities.

Why it matters

Potential benefit: If successful, this approach could significantly improve mobility and reduce pain for patients suffering from neurological and gynaecological conditions.

How similar studies have gone: While the use of tDCS in neurological rehabilitation has shown promise in other studies, this specific application in both neurological and gynaecological conditions is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion 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.

Where it's running

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

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.