Tokyo, Oct. 17 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000063309) titled 'Effects of a cognitive task on the process of motor learning' on Oct. 16.

Study Type: Interventional

Study Design: Basic Design - Parallel Randomization - Randomized Blinding - Single blind -participants are blinded Control - Placebo

Primary Sponsor: Institute - Tokoha University

Condition: Condition - Healthy adults Classification by malignancy - Others Genomic information - NO

Objective: Narrative objectives1 - The aim of this study is to examine the effects of a Stroop task performed before motor practice on motor learning, the learning process, and next-day retention during a visuomotor adaptation task in healthy university students. Basic objectives2 - Efficacy

Intervention: Interventions/Control_1 - Stroop task group Participants perform one 15-min Stroop task on Day 1. They are instructed to respond according to the ink color of the presented color word rather than its semantic meaning. After the Stroop task, participants rest for 30 s and then perform 100 trials of a visuomotor adaptation task with a 75-degree visual rotation. The intervention is administered once on a single day. Interventions/Control_2 - Control task group Participants perform one 15-min control task on Day 1. They are instructed to respond according to the color of a neutral stimulus (XXXX). After the control task, participants rest for 30 s and then perform 100 trials of a visuomotor adaptation task with a 75-degree visual rotation. The intervention is administered once on a single day.

Eligibility: Age-lower limit - 18 years-old <= Age-upper limit - Not applicable Gender - Male and Female Key inclusion criteria - 1. Right-handed university students aged 18 years or older. 2. Individuals who understand the purpose and procedures of the study and provide written informed consent. Key exclusion criteria - 1. Individuals who self-report pain, orthopedic disorders, or neurological disorders that may interfere with upper-limb movement. 2. Individuals with a history of psychiatric disorders. 3. Individuals judged to have difficulty perceiving the visual stimuli or performing the experimental tasks. Target Size - 40

Recruitment Status: Recruitment status - Preinitiation Date of protocol fixation - 2026 Year 05 Month 27 Day Date of IRB - 2026 Year 06 Month 17 Day Anticipated trial start date - 2026 Year 10 Month 26 Day Last follow-up date - 2026 Year 12 Month 31 Day

To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000072447

Disclaimer: Curated by HT Syndication.