Actively Recruiting
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
Eligibility Criteria
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
You will not qualify if you...
- No written consent to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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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