Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
Healthy Volunteers
ID06891690

Use of TDCS Stimulation in Neurological and Gynaecological Conditions

Led by Poznan University of Physical Education · Updated on 2025-03-24

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the use of transcranial direct current stimulation (tDCS) to improve limb function in neurological patients and reduce pain in women with certain gynecological conditions. The study includes adults aged 18 to 90 years with impairments from stroke, spinal cord, or nerve root disorders, as well as women aged 18 to 70 years with conditions like endometriosis and painful menstruation. The study aims to assess the impact of tDCS on quality of life using standardized questionnaires before and after treatment. Participants will receive tDCS stimulation sessions, ranging from 1 to 10 treatments depending on their group. Neurological patients undergo rehabilitation with or without tDCS, involving assessments like body composition, skin properties, postural stability, reaction times, and muscle strength. Gynecological patients receive tDCS sessions of 3, 5, or 10 treatments and complete questionnaires on quality of life and sexual satisfaction. Treatments are administered while seated, with current intensities up to 2 mA for about 20-30 minutes. During the study, participants undergo multiple evaluations including biomechanical measurements, reaction time tests, muscle strength assessments, and various health and quality of life questionnaires. These assessments occur before and after stimulation sessions, with follow-up lasting up to one year. Researchers will monitor outcomes such as limb function, pain levels, and quality of life changes. The study also includes healthy volunteers for comparison and aims to share results through scientific publications and conferences.

CONDITIONS

Brief Title

Use of TDCS Stimulation in Neurological and Gynaecological Conditions

Who Can Participate

Age: 18Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 90 years with impairment of upper and lower limb function due to neurological conditions such as stroke, spinal cord, or nerve root disorders
  • Women aged 18 to 70 years with selected gynecological conditions including endometriosis, painful menstruation, dyspareunia, or polycystic ovary syndrome
  • Gynecological patients must not be receiving any treatment other than tDCS stimulation
  • Ability to provide written consent to participate in the study
Not Eligible

You will not qualify if you...

  • No written consent to participate in the study

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 1 to 3 months for neurological participants; up to 10 tDCS sessions for gynecological participants

Participants receive tDCS stimulation sessions combined with assessments and rehabilitation as applicable, to improve neurological or gynecological conditions.

1 to 10 visits depending on number of tDCS stimulations; sessions typically daily from Monday to Friday

Follow-up

Duration - Up to 1 year

Participants complete questionnaires and undergo assessments to evaluate treatment effects over up to 1 year.

Periodic assessments during follow-up; exact visit schedule varies

Trial Site Locations

Total: 1 location

1

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

Poznan, Poland, 61-871

Actively Recruiting

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Research Team

M

Małgorzata Wójcik, PhD PT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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