← Back to Clinical Trials
Recruiting NCT06891690

NCT06891690 Use of TDCS Stimulation in Neurological and Gynaecological Conditions

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
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

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 90 Years
Study Type INTERVENTIONAL
Interventions
tDSC stimulation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 300 participants in total. It began in 2025-02-05 with a primary completion date of 2025-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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.

Contact & Investigator

Central Contact

Małgorzata Wójcik, PhD PT

✉ m.wojcik@awf-gorzow.edu.pl

📞 +48(95) 72 79 100

Frequently Asked Questions

Who can join the NCT06891690 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 90 Years, studying Stroke. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06891690 currently recruiting?

Yes, NCT06891690 is actively recruiting participants. Contact the research team at m.wojcik@awf-gorzow.edu.pl for enrollment information.

Where is the NCT06891690 trial being conducted?

This trial is being conducted at Poznan, Poland.

Who is sponsoring the NCT06891690 clinical trial?

NCT06891690 is sponsored by Poznan University of Physical Education. The trial plans to enroll 300 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology