Using tDCS stimulation to improve function and reduce pain in neurological and gynaecological patients
Use of TDCS Stimulation in Neurological and Gynaecological Conditions
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
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 300 (estimated) |
| Ages | 18 Years to 90 Years |
| Sex | All |
| Sponsor | Poznan University of Physical Education Academic / other |
| Locations | 1 site (Poznan) |
| Trial ID | NCT06891690 on ClinicalTrials.gov |
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.
Who should consider this trial
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.
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.
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 performed: 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.
Eligibility criteria
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 this trial is running
Poznan
- 1Department of Physiotherapy, Poznan University of Physical Education, Faculty of Sport Sciences in Gorzow Wlkp., 61-871 Poznan — Poznan, Poland (Recruiting)
Study contacts
- Study coordinator: Małgorzata Wójcik, PhD PT
- Email: m.wojcik@awf-gorzow.edu.pl
- Phone: +48(95) 72 79 100
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.