Cause-effect Relationships Between Brain Networks and Bimanual Coordination in Older Adults

NCT ID: NCT04349137

Last Updated: 2021-08-30

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-11-01
• Study Completion Date: 2021-09-30

Brief Summary

In this study, high-definition dual-site transcranial alternating current stimulation (i.e., non-invasive brain stimulation) will be applied to boost the fronto-parietal network during a bimanual coordination task in healthy young and older adults. Previous studies indicated that this network is important in initial motor learning, possibly through its role in spatial working memory. Therefore, stimulation will be applied during both a pure spatial working memory test, and during a bimanual coordination task.

It is also shown that healthy older adults do not engage spatial working memory brain regions during motor learning, which is related to worse motor learning. Therefore, the investigators will investigate whether this type of stimulation can improve bimanual motor learning in healthy older adults.

Detailed Description

A single-blind, pseudo-randomised, sham-controlled within-subject design will be used. The study consists of three experimental sessions. In each session, one out of three stimulation conditions was applied: (1) in-phase stimulation; (2) anti-phase stimulation; (3) sham stimulation. The order of the three stimulation conditions over sessions will be pseudo-randomised across participants. Within each session, stimulation is applied during the performance of two tasks: a 2-back task for assessing pure spatial working memory (sWM), and a complex bimanual tracking task (BTT) for assessing bimanual skill acquisition. To minimise learning and carry-over effects over sessions, a wash-out period of 6 weeks in between sessions is used and three different variants of the BTT task (one for each session). The order of these variants was also pseudo-randomised across participants.

For assessing sWM, participants perform an adapted version of the 2-back visuospatial match-to-sample test used in Alekseichuk et al., 2016. Participants are seated on a chair, with their right hand resting on a response box. A computer screen is placed in front of the participant. On the screen, a blue 3x3 grid is drawn on a black background. Each trial consists of three events: a stimulus, a probe, and a response period. During the stimulus, two or three white dots appear somewhere in the grid for 2150ms. After a time interval of 50ms, this is followed by the appearance of the probe, consisting of one small blue dot, lasting for 300ms. During the response period (2000ms duration), the participant is requested to either press or to not press the response button, indicating whether the location of the probe matches the location of the stimulus in the previous trial or not (i.e., 2-back condition).

For familiarisation purposes, participants are first instructed what the goal of the task is. Next, they practiced a series of ten or twenty trials without stimulation.

For the experiment (i.e., task performance during stimulation), a complete set of trials is organised in five blocks, consisting of 30 trials (i.e. 150 trials per set). The five blocks are separated by 1-minute breaks. The distribution of 2-dot or 3-dot stimulus conditions in the 150-trial set was 50%-50%, presented in random order. Forty % of the trials are matched trials (i.e. 58 trials) and 60% are non-matched trials (i.e. 87 trials).

For this study, we use three fixed sets of trials, i.e. one for each session. The order of these sets over sessions will be pseudo-randomised across participants.

For assessing initial bimanual learning, we use a complex visuomotor bimanual tracking task (BTT). Participants are seated in front of a computer screen with their arms pronated on the table. Each index finger is placed in a controller. The controllers are two rotatable dials with small grooves for finger placement. By bimanually rotating the two dials, the participant can move the position of a red cursor on the display. Left and right dial rotations induced cursor movement along the ordinate and abscissa.

The goal of the BTT is to manipulate the cursors' position in order to follow a moving target dot on a straight inclined line, presented on the display, as accurately as possible. Each BTT trial starts with the appearance of the target line. At the origin of this line, in the center of the display, a red target dot is presented for 2 seconds (i.e. preparation period). Then, an auditory GO-signal indicates the start of the movement period: the target dot begins to move at a constant speed along the line towards the peripheral end of the line, which the participant has to follow by rotating the dials simultaneously. The duration of the target dot movement from center to periphery (i.e. movement period) is 5 seconds. Between trials, a time interval of 3 seconds is implemented.

There are four different task conditions that differ in relative inter-hand frequencies (1:3 vs. 3:1) and relative directionality of the rotating dials (iso-directional [ISO] vs. non-iso-directional [NON-ISO]). More specifically, in the 1:3 condition, the right index finger has to rotate the dial three times faster than the left hand, while in the 3:1 condition, this pattern is reversed. For the ISO mode, both index fingers have to rotate the dials either to the right (ISO-R) or left (ISO-L). For the NON-ISO mode, both index fingers have to rotate the dials either inward (NON-ISO-IN) or outward (NON-ISO-OUT).

To get familiar with the task, a practice block of 16 trials without stimulation is implemented. For the experiment (i.e. task performance during stimulation), there are four blocks of 36 trials, where each task condition is repeated nine times in each block. We provide 1-minute breaks between blocks. Fifteen minutes after the end of the fourth block, a retention block of 36 trials without stimulation will be added. The order of the four task conditions within each block will be randomised.

To minimize learning effects over the three sessions, we rotated the reference frame of line orientation each time with 90 degrees.

Stimulation will be delivered by two battery-driven Direct Current (DC) stimulator PLUS devices (neuroConn and Eldith GmbH, Ilmenau, Germany). Each device is connected to a center-surround rubber ring montage, suited for focal stimulation. Each montage consists of a small circular center electrode (diameter of 20 mm) and a surrounding ring electrode (inner diameter of 40 mm and outer diameter of 60 mm). The center electrodes are positioned according to the 10-20 EEG system: in the middle between AF4 and F4, which corresponds to the junction between BA9 and BA46 (i.e. right dorsolateral prefrontal cortex (DLPFC)); and P4, which corresponds to the right posterior parietal cortex (PPC). Impedance is kept below 10kOhm using a conductive paste (Ten20, Weaver and Company, CO, USA).

In-phase stimulation will consist of 6Hz stimulation over the right DLPFC and the right PPC that is synchronized (0deg phase lag between both sites), while anti-phase stimulation will use desynchronized 6Hz stimulation (180deg phase lag between both sites). To ensure a consistent phase lag, stimulation will be applied for 1min, then stopped and restarted after 5s. The sham stimulation will make use of vibrations at 6Hz instead of electrical current to mimic the physical throbbing sensation.

Conditions

Healthy Aging; Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: SINGLE

Study Groups

In-phase 6Hz tACS

Transcranial alternating current stimulation (tACS) will be administered over the right PPC and the right DLPFC in a synchronized (in-phase) manner at a frequency of 6Hz

Group Type: EXPERIMENTAL

HD-tACS

Intervention Type: DEVICE

non-invasive high-definition dual-site transcranial alternating current stimulation (HD-tACS) low intensive electrical alternating currents (2 mA peak-to-peak) are externally applied to the skull at a frequency of 6Hz to entrain endogenous neural oscillatory activity.

Anti-phase 6Hz tACS

Transcranial alternating current stimulation (tACS) will be administered over the right PPC and the right DLPFC in a desynchronized (anti-phase, i.e. with a difference of 180deg) manner at a frequency of 6Hz

Group Type: ACTIVE_COMPARATOR

HD-tACS

Intervention Type: DEVICE

non-invasive high-definition dual-site transcranial alternating current stimulation (HD-tACS) low intensive electrical alternating currents (2 mA peak-to-peak) are externally applied to the skull at a frequency of 6Hz to entrain endogenous neural oscillatory activity.

Sham tACS

A sham transcranial alternating current stimulation (tACS) will be administered over the right PPC and the right DLPFC at a frequency of 6Hz using physical vibrations instead of electrical current

Group Type: SHAM_COMPARATOR

sham HD-tACS

Intervention Type: DEVICE

sham non-invasive high-definition dual-site transcranial alternating current stimulation (HD-tACS)

Interventions

HD-tACS

non-invasive high-definition dual-site transcranial alternating current stimulation (HD-tACS) low intensive electrical alternating currents (2 mA peak-to-peak) are externally applied to the skull at a frequency of 6Hz to entrain endogenous neural oscillatory activity.

Intervention Type: DEVICE

sham HD-tACS

sham non-invasive high-definition dual-site transcranial alternating current stimulation (HD-tACS)

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Right-handedness
• Normal cognitive functions (>25 on Montreal Cognitive Assessment Questionnaire)
• Normal vision
• Healthy

Exclusion Criteria

• Transcranial Electric Stimulation (TES) is contra-indicated (TES screening questionnaire)
• Neurologic or psychiatric disorders
• Physical disorder(s) that might interfere with the execution of the bimanual motor task
• Alcohol and/or drug addiction
• Active smokers
• Current use of specific drugs that interfere with the central nervous system
• Skin allergies to cosmetics and lotions
• Pregnancy

• Minimum Eligible Age: 65 Years
• Maximum Eligible Age: 77 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Hasselt University

OTHER

Sponsor Role: lead

Responsible Party

prof. dr. Raf Meesen

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Bart Van Wijmeersch, prof. dr.

Role: STUDY_DIRECTOR

Hasselt University

Raf Meesen, prof. dr.

Role: PRINCIPAL_INVESTIGATOR

Hasselt University

Stefanie Verstraelen, drs.

Role: STUDY_CHAIR

Hasselt University

Kim van Dun, dr.

Role: STUDY_CHAIR

Hasselt University

Locations

Hasselt University

Hasselt, , Belgium

Site Status: RECRUITING

Countries

Belgium

Central Contacts

Raf Meesen, prof. dr.

Role: CONTACT

raf.meesen@uhasselt.be

+32 11 26 21 24

Stefanie Verstralen, drs.

Role: CONTACT

stefanie.verstraelen@uhasselt.be

+32 11 26 93 61

Facility Contacts

Stefanie verstraelen, drs.

Role: primary

stefanie.verstraelen@uhasselt.be

+32 11 26 93 61

Kim van Dun, dr.

Role: backup

kim.vandun@uhasselt.be

Other Identifiers

RWS-SV-001

Identifier Type: -

Identifier Source: org_study_id