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Priming Expectations and Motor Learning With tDCS

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The purpose of this study is to test if priming expectations of transcranial Direct Current Stimulation (tDCS) can improve the efficacy of tDCS in enhancing motor learning.

Official Title

Effects of Modulating Expectations About Noninvasive Brain Stimulation on Motor Learning

Quick Facts

Study Start:2023-10-23

Study Completion:2025-04-16

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:COMPLETED

Study ID

NCT06039605

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* Must be 18 or older. Right-hand dominant * Right-hand dominant	* Mixed-handed or ambidextrous * Left-hand dominant * Seizure(s) * Head injury resulting in a loss of consciousness that has required further investigation (including neurosurgery) * Migraines * Current medical diagnosis of a phycological or neurological condition * Any metal in head (outside of mouth) such as shrapnel or surgical clips * Any implanted devices (e.g. cardiac pacemaker, brain stimulator) * Skin condition on scalp (e.g. psoriasis) * Head wound that has not completely healed * Adverse reactions to tDCS or any other brain stimulation technique (e.g. TMS, tRNS) * Pregnant * Currently taking prescription medications or are self-medicating (including recreational drug use), other than the contraceptive pill?

Inclusion Criteria

Exclusion Criteria

* Must be 18 or older. Right-hand dominant
* Right-hand dominant

* Mixed-handed or ambidextrous
* Left-hand dominant
* Seizure(s)
* Head injury resulting in a loss of consciousness that has required further investigation (including neurosurgery)
* Migraines
* Current medical diagnosis of a phycological or neurological condition
* Any metal in head (outside of mouth) such as shrapnel or surgical clips
* Any implanted devices (e.g. cardiac pacemaker, brain stimulator)
* Skin condition on scalp (e.g. psoriasis)
* Head wound that has not completely healed
* Adverse reactions to tDCS or any other brain stimulation technique (e.g. TMS, tRNS)
* Pregnant
* Currently taking prescription medications or are self-medicating (including recreational drug use), other than the contraceptive pill?

Contacts and Locations

Principal Investigator

Sydney Schaefer, PhD

PRINCIPAL_INVESTIGATOR

Arizona State University

Study Locations (Sites)

Arizona State University

Tempe, Arizona, 85281

United States

Collaborators and Investigators

Sponsor: Arizona State University

Sydney Schaefer, PhD, PRINCIPAL_INVESTIGATOR, Arizona State University

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-10-23

Study Completion Date2025-04-16

Study Record Updates

Study Start Date2023-10-23

Study Completion Date2025-04-16

Terms related to this study

Keywords Provided by Researchers

tDCS

Additional Relevant MeSH Terms

Expectations
Motor Learning