Use of TDCS Stimulation in Neurological and Gynaecological Conditions
Recruiting · NCT06891690 · Interventional (participants receive a specific treatment) · Lead sponsor: Poznan University of Physical Education
View the official record on ClinicalTrials.gov →Interventions studied
tDSC stimulation
What this trial is about
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.
Who can take part
Age range
18 Years to 90 Years
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
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 is running
2 locations listed.
- 1Department of Physiotherapy, Poznan University of Physical Education, Faculty of Sport Sciences in Gorzow Wlkp., 61-871 Poznan - Poznan, Poland
- 1Department of Physiotherapy, Poznan University of Physical Education, Faculty of Sport Sciences in Gorzow Wlkp., 61-871 Poznan - Poznan, Poland