Using tDCS to Enhance Learning of a New Walking Pattern

The ability to change walking patterns is important for daily tasks such as stepping over an obstacle. This change of walking pattern can occur in a strategic manner, i.e., consciously making one step longer or shorter. Healthy individuals can learn a new walking pattern through perturbed visual feedback of their walking information (Kim et al., 2015; Kim et al., 2017). This type of learning is thought to largely involve explicit strategy. Transcranial direct current stimulation (tDCS) is a form of non-invasive brain stimulation that can enhance learning of some motor tasks (Reis et al., 2009), and primarily has been studied in the upper extremity. In locomotor learning, prior recent work by the investigators has suggested that tDCS does not affect non-strategy based locomotor learning, and the investigators speculate that tDCS may benefit learning of strategic tasks instead. The purpose of this study is to determine if tDCS can enhance learning and retention of a new walking pattern in a strategy-based, visually guided locomotor task in healthy individuals. Two groups of young, healthy participants will be recruited to learn a new walking pattern through perturbed visual feedback, with retention of learning tested on the second day. One group will receive tDCS, which is expected to enhance learning. The other group will receive placebo stimulation and serve as a control. Results from this work will provide information on which type of motor learning is sensitive to enhancement with tDCS, and may help pave the path for utilizing tDCS for neurorehabilitation.

Study Overview

• Status: Withdrawn
• Conditions: no Condition Being Studied; tDCS Only in Healthy Subjects
• Intervention / Treatment: Procedure: tDCS

• Study Type: Interventional
• Phase: Not Applicable

Contacts and Locations

Study Locations

• United States
  • Delaware
    • Newark, Delaware, United States, 19713
      • University of Delaware

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 40 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Age 18-40 years
• Medically stable and generally healthy
• Able to walk on a treadmill without the use of handrails for 20 minutes at a speed of 1.0 m/s without rest
• Resting heart rate ≤100 beats per minute
• Resting blood pressure ≤140/90 mm Hg
• Willing and able to attend all testing sessions

Exclusion Criteria:

• Any chronic or recent medical conditions, including any musculoskeletal, cardiovascular, pulmonary, psychiatric or neurological diagnosis
• Any impaired sensation or weakness in either lower extremity
• History of serious traumatic head injury, defined as a loss of consciousness for more than 5 minutes and/or requiring medical treatment
• Any history of acute or chronic problems with balance or more than 1 fall in the last 12 months
• History of brain surgery
• Taking 4 or more medications
• Current or chronic pain located anywhere in the body
• History of seizures
• Currently pregnant (if a female of childbearing age)
• Currently taking any medications that act on the central nervous system
• Implanted pumps or stimulators above the shoulders
• Metal aneurysm, other metal surgical clip placement, or any other metal in the head, face, or neck, except for dental fillings

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Basic Science
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Real tDCS; Anodal transcranial direct current stimulation (tDCS) targeting the primary motor cortex delivered via saline-soaked sponge electrodes (anode, 8 cm^2; cathode 38.4 cm^2) at an intensity of 1.5 milliamperes over < 30 minutes.	Procedure: tDCS; real or sham tDCS delivered to primary motor cortex
Sham Comparator: Control; Anodal transcranial direct current stimulation (tDCS) targeting the primary motor cortex delivered via saline-soaked sponge electrodes (anode, 8 cm^2; cathode 38.4 cm^2) at an intensity of 1.5 milliamperes over 2 minutes.	Procedure: tDCS; real or sham tDCS delivered to primary motor cortex

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Magnitude of Locomotor Learning	Step length produced on the perturbed leg at the end of the learning period on study day 1 and subtracted from baseline (pre-learning period) step length	study day 1
Magnitude of Locomotor Learning Retention	Step length produced on the perturbed leg on study day 2, normalized to the Magnitude of Locomotor Learning achieved on study day 1	study day 2

Collaborators and Investigators

• Sponsor: University of Delaware
• Investigators: Principal Investigator: Susanne M Morton, PhD, PT, University of Delaware

Study record dates

Study Major Dates

• Study Start (Actual): July 16, 2018
• Primary Completion (Actual): April 10, 2019
• Study Completion (Actual): April 10, 2019

Study Registration Dates

• First Submitted: June 14, 2018
• First Submitted That Met QC Criteria: June 27, 2018
• First Posted (Actual): July 11, 2018

Study Record Updates

• Last Update Posted (Actual): April 1, 2020
• Last Update Submitted That Met QC Criteria: March 30, 2020
• Last Verified: March 1, 2020

More Information

Terms related to this study

• Keywords: tDCS; motor learning; locomotion
• Other Study ID Numbers: 1240484

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