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Study identifier: NCT07619703 Synced from ClinicalTrials.gov · July 28, 2026
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Effects of a Neurorehabilitation Program Based on CIMT and Non-invasive Neuromodulation Through C-tDCS on the Recovery of Paretic Upper Limb Function, Quality of Life, and Therapeutic Alliance in Women From the Araucanía Region Who Suffered a Stroke (CIMT + tDCS).

Condition: Stroke  ·  Sponsor: Universidad de La Frontera

PhaseNA
Planned participants24
Who can joinFemale, 30 Years to 85 Years
Healthy volunteersNo

About this study

General Objective To determine the effects of a neurorehabilitation program based on Constraint-Induced Movement Therapy (CIMT) and non-invasive neuromodulation through cerebellar transcranial direct current stimulation (C-tDCS) on the recovery of paretic upper limb function, quality of life, and therapeutic alliance in women from the Araucanía Region who suffered a stroke. Methodology An experimental design consisting of a single-blind randomized controlled clinical trial is proposed. The study will include two independent groups of women diagnosed with stroke, who will participate in five assessment time points (pre-treatment, intermediate, post-treatment, and two follow-ups). Motor function (Motor Activity Log-30 and ARAT), quality of life (ECVI-38), and therapeutic alliance (CAF-P) will be evaluated. The intervention includes 10 sessions (120 minutes each), delivered daily over a two-week period. The experimental group (EG) will receive CIMT combined with C-tDCS, while the control group (CG) will receive CIMT plus sham C-tDCS (using the standard safety sham protocol commonly known as "FISSFO" \[Fade In of Stimulation, Brief Real Stimulation, Fade Out\]). In both groups, C-tDCS will be applied during the first 20 minutes of the session simultaneously with the practice of specific upper-limb motor tasks, followed by 100 minutes of CIMT. The CG will receive the same intervention but with sham stimulation, applying current for one minute to generate the initial sensation with…

This description comes directly from the study's public registry record.

Talk to the study team

Arlette Doussoulin, PhD  ·  +56997445912  ·  arlette.doussoulin@ufrontera.cl

Always discuss trial participation with your own doctor first.

Locations (1)

Universidad de La Frontera, Temuco, Chile.Temuco, Araucania, ChileRecruiting

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Source record: clinicaltrials.gov/study/NCT07619703