Trials / Recruiting
RecruitingNCT06149897
Feasibility and Effectiveness of tDCS in the Treatment of Post-stroke Fatigue (EFECTS).
Feasibility and Effectiveness of Tdcs in a Multimodal Treatment With Health Education and Aerobic Exercise in the Treatment of Post-stroke Fatigue.
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 54 (estimated)
- Sponsor
- Hospital Clinic of Barcelona · Academic / Other
- Sex
- All
- Age
- 18 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
This study aims to analyze the use of non-invasive brain stimulation (tDCS) is beneficial for the treatment of post-stroke fatigue.
Detailed description
A single-blind randomized clinical trial will be conducted. The intervention will consist of 8 20-minute tDCS sessions conducted over four weeks. The stimulation will be performed by applying the stimulation to the dorsolateral prefrontal cortex on the left side (F3) and the cathode will be at point O2 of the right hemisphere. The study will consist of two groups: the control group in which sham stimulation will be applied and therapeutic education and aerobic exercise; the intervention group in which stimulation, therapeutic education and therapeutic exercise will be carried out.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | tDCS | Non invasive brain stimulation with sham and active comparators |
Timeline
- Start date
- 2023-11-10
- Primary completion
- 2025-12-05
- Completion
- 2026-02-05
- First posted
- 2023-11-29
- Last updated
- 2025-09-24
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT06149897. Inclusion in this directory is not an endorsement.