Clinical Trials Directory

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

TypeNameDescription
DEVICEtDCSNon 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.