The Effect of Intermittent Theta Burst Stimulation on Motor Learning in Healthy Adults

February 13, 2022 updated by: Esma Nur KOLBAŞI, Istanbul Medeniyet University
This study investigates the effect of different application frequencies of intermittent theta burst stimulation on motor learning in healthy adults.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

10

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Istanbul, Turkey
        • İstanbul Bakırköy Ruh ve Sinir Hastalıkları Hastanesi

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.

Eligibility Criteria

Ages Eligible for Study

40 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • being at the age of 40-75 years

Exclusion Criteria:

  • visual disability
  • cognitive or psychiatric problems such as dementia, depression, etc.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Finger Taping Task + iTBS intermittent group
Finger Taping Task + iTBS Daily application group: the group receives these applications every other day for 5 sessions.
Other: neuromodulation
neuromodulation: Neuromodulation is technology that acts directly upon nerves. It is the alteration-or modulation-of nerve activity by delivering electrical or magnetic stimulus/current.
Active Comparator: Finger Taping Task intermittent Group
Finger Taping Task intermittent application group: the group receives the application every other day for 5 sessions.
Other: motor learning training
motor learning training requires performing a sequential training called finger taping task

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Finger Taping Task
Time Frame: 5 minutes
The total right answers and the mean response time in the finger taping task will be recorded
5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Istanbul Medeniyet University

Collaborators

Istanbul University - Cerrahpasa (IUC)

Investigators

  • Study Director: Burcu Ersoz Huseyinsinoglu, PhD, Istanbul University - Cerrahpasa (IUC)

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 Major Dates

Study Start (Actual)

November 1, 2021

Primary Completion (Actual)

February 4, 2022

Study Completion (Actual)

February 5, 2022

Study Registration Dates

First Submitted

October 7, 2021

First Submitted That Met QC Criteria

October 7, 2021

First Posted (Actual)

October 11, 2021

Study Record Updates

Last Update Posted (Actual)

March 2, 2022

Last Update Submitted That Met QC Criteria

February 13, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • IstanbulMU21

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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