Language & Cognitive Control

NCT ID: NCT05272397

Last Updated: 2022-04-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-11-26

Study Completion Date

2021-12-02

Brief Summary

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Catecholamine (CA) neurotransmitters, such as dopamine (DA) and noradrenaline (NA), have long been implicated playing a critical role in cognitive functions, such as working memory (WM), inhibition, learning, and decision making. Recent evidence from neurodegenerative patients and the healthy population suggested that CA also influences language processing. However, the question of what kind of influence that CA might exert on language is still open. Some previous studies have shown that CA can enhance semantic processing. In a recent study it was observed that CA agonists (i.e., methylphenidate) enhance participant's sensitivity to semantically incongruent information even when language processing was actually goal-irrelevant. On the other hand, the processing of semantically congruent information was enhanced while language processing was the goal. Moreover, consistent with some previous findings that there is a relation between participants' baseline characteristics and MPH effects, it was observed that participants with lower WM capacity benefited more from receiving methylphenidate. These results shed light on the relation between CA and language processing, but also lead to further questions, such as whether the interaction between CA and semantic processing is language-specific or mediated by the relation between CA and more general cognitive functions (e.g., WM, inhibition), and whether CA also has an influence on other aspects of language processing, such as syntactic processing. The present study aimed to further investigate the nature of the relation between CA and language processing by administrating methylphenidate (MPH) to healthy participants. MPH is an indirect CA agonist, which is the most commonly prescribed drug for attention deficit/hyperactivity disorder (ADHD). Previous studies have shown that MPH can efficiently increase the extracellular levels of CA in the brain by blocking their reuptake.

Objective: The primary objectives are: 1) to further investigate the effect of CA on semantic processing. The study plans to examine whether MPH interacts with processing of sentence context constraints via its influence on cognitive control operations. 2) To investigate the effects of MPH on syntactic processing. More specifically, the study is interested in whether MPH has an influence on revising syntactically temporarily ambiguous sentences.

A secondary objective is to further examine the relation between MPH effects and the baseline characteristics of individual participants.

Study design: This study will use a within-subject, double-blind, placebo-controlled, randomized, crossover design.

Study population: Approximately 40 healthy native Dutch speakers between 18 and 45 years old will be recruited. All subjects will have to complete one screening session and two separate testing sessions within three different days at the Donders Centre for Cognitive Neuroimaging (DCCN).

Intervention: Participants will either orally receive a 20mg methylphenidate or placebo capsule in each of the two testing sessions. Methylphenidate has been approved for clinical use in the Netherlands and the drug can be administered safely without any relevant risk of serious adverse events.

Main study parameters: Primary study parameters will include sentence comprehension capacity, attention and processing speed. In addition, several other measures will be included to monitor participants' baseline characteristics (e.g. working memory capacity, vocabulary size) and the general modulation effects of MPH (e.g. heart rate, blood pressure, subjective feeling).

Hypotheses:

Based on the previous finding that methylphenidate improves cognitive stability while it impairs flexible updating, the hypothesis is that methylphenidate will hinder participants' performance in resolving syntactic ambiguity, which requires an immediate updating and revising of an initial interpretation. This should be reflected in event-related potential (ERP) measures related to revision, namely the P600 effect is predicted to be reduced in the drug condition compared to placebo.

Detailed Description

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Conditions

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Language Methylphenidate of Undetermined Intent

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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Drug Session

In this arm of the study participants receive the drug (Methylphenidate - 20mg), administered prior to completion of the primary and secondary tasks for the study.

Electroencephalography (EEG) is measured for the duration of the primary and secondary tasks. Participants complete both arms of the study, and the order in which participants are assigned to this and the other arm of the study is randomized.

Group Type ACTIVE_COMPARATOR

Methylphenidate 20 Mg Oral Tablet

Intervention Type DRUG

20mg methylphenidate or placebo capsule - one per session (counterbalanced) approximately 1 week apart

Language Task

Intervention Type BEHAVIORAL

The core part of the experiment is the language task, in which the aim is to investigate two critical aspects of language processing: semantic and syntactic processing. In this task, participants will be asked to read a list of sentences.

Rest Recording

Intervention Type BEHAVIORAL

Brain activity in the EEG is recorded at rest with eyes open and eyes closed to obtain baseline measures of alpha power as a proxy for attention and control under conditions of drug and placebo.

Go/No-Go Task

Intervention Type BEHAVIORAL

A Go/No-Go task will be implemented in the study design to investigate the functional properties of spatial selective attention and response inhibition. An adapted cued Go/No-Go paradigm from Randall \& Smith (2011) will be employed.

Processing Speed

Intervention Type BEHAVIORAL

A speeded button response task will be included to measure participants' general processing speed. In this task, participants will be instructed to respond to a simple shape presented in the centre of the screen as fast and accurately as possible through pressing a corresponding button.

Placebo Session

In this arm of the study participants receive the a placebo, administered prior to completion of the primary and secondary tasks for the study.

Electroencephalography (EEG) is measured for the duration of the primary and secondary tasks. Participants complete both arms of the study, and the order in which participants are assigned to this and the other arm of the study is randomized.

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

20mg methylphenidate or placebo capsule - one per session (counterbalanced) approximately 1 week apart

Language Task

Intervention Type BEHAVIORAL

The core part of the experiment is the language task, in which the aim is to investigate two critical aspects of language processing: semantic and syntactic processing. In this task, participants will be asked to read a list of sentences.

Rest Recording

Intervention Type BEHAVIORAL

Brain activity in the EEG is recorded at rest with eyes open and eyes closed to obtain baseline measures of alpha power as a proxy for attention and control under conditions of drug and placebo.

Go/No-Go Task

Intervention Type BEHAVIORAL

A Go/No-Go task will be implemented in the study design to investigate the functional properties of spatial selective attention and response inhibition. An adapted cued Go/No-Go paradigm from Randall \& Smith (2011) will be employed.

Processing Speed

Intervention Type BEHAVIORAL

A speeded button response task will be included to measure participants' general processing speed. In this task, participants will be instructed to respond to a simple shape presented in the centre of the screen as fast and accurately as possible through pressing a corresponding button.

Intake Session

In this arm of the study participants are screened for suitability to participate in the experiment based on specified inclusion and exclusion criteria. They also complete some baseline tasks to assess working memory capacity, impulsiveness, and subjective mood.

Group Type OTHER

Operation Span

Intervention Type BEHAVIORAL

In the operation span task, participants are instructed to solve math operations (e.g., (1\*2) +1=?) as soon as possible and then remember a single letter. This to-be-remembered letter is followed by either another math-word combination or a recall screen, which will show up at the end of each set. When the recall screen is presented, participants have to recall all the letters in the correct order they were presented. The experimental trials contain three sets at each set size (i.e., the number of math-word pairs), with set sizes ranging from 3 to 7 items. This results in a total of 75 sets with 75 letters and 75 math problems. The order of set sizes is random for each participant. Participants' operation span will be evaluated by the total number of letters recalled in the correct serial position regardless of whether the entire trial was recalled correctly.

Reading Span

Intervention Type BEHAVIORAL

Participants are instructed to judge whether a presented sentence makes sense or not. After each sentence, a to-be-remembered letter will be shown on the screen, which is followed by either another sentence-word combination or the final recall screen. The set size ranges from 3 to 7 items. At the end of each set of sentences, participants will be required to recall all the letters in the current set in order. There will be a total of 75 letters and 75 sentence judgements. The order of the set sizes will be at random for each participant. Participants' performance will be evaluated by calculating the total number of correctly recalled letter sets.

Barratt Impulsiveness Scale

Intervention Type BEHAVIORAL

The Barratt impulsiveness scale (BIS-11) will be used in the experiment to measure participants' trait impulsivity. Participants will be required to rate themselves on 30 items that are related to attention, motor, self-control, cognitive complexity, perseverance, and cognitive instability impulsiveness.

Interventions

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Methylphenidate 20 Mg Oral Tablet

20mg methylphenidate or placebo capsule - one per session (counterbalanced) approximately 1 week apart

Intervention Type DRUG

Placebo

20mg methylphenidate or placebo capsule - one per session (counterbalanced) approximately 1 week apart

Intervention Type DRUG

Language Task

The core part of the experiment is the language task, in which the aim is to investigate two critical aspects of language processing: semantic and syntactic processing. In this task, participants will be asked to read a list of sentences.

Intervention Type BEHAVIORAL

Rest Recording

Brain activity in the EEG is recorded at rest with eyes open and eyes closed to obtain baseline measures of alpha power as a proxy for attention and control under conditions of drug and placebo.

Intervention Type BEHAVIORAL

Go/No-Go Task

A Go/No-Go task will be implemented in the study design to investigate the functional properties of spatial selective attention and response inhibition. An adapted cued Go/No-Go paradigm from Randall \& Smith (2011) will be employed.

Intervention Type BEHAVIORAL

Processing Speed

A speeded button response task will be included to measure participants' general processing speed. In this task, participants will be instructed to respond to a simple shape presented in the centre of the screen as fast and accurately as possible through pressing a corresponding button.

Intervention Type BEHAVIORAL

Operation Span

In the operation span task, participants are instructed to solve math operations (e.g., (1\*2) +1=?) as soon as possible and then remember a single letter. This to-be-remembered letter is followed by either another math-word combination or a recall screen, which will show up at the end of each set. When the recall screen is presented, participants have to recall all the letters in the correct order they were presented. The experimental trials contain three sets at each set size (i.e., the number of math-word pairs), with set sizes ranging from 3 to 7 items. This results in a total of 75 sets with 75 letters and 75 math problems. The order of set sizes is random for each participant. Participants' operation span will be evaluated by the total number of letters recalled in the correct serial position regardless of whether the entire trial was recalled correctly.

Intervention Type BEHAVIORAL

Reading Span

Participants are instructed to judge whether a presented sentence makes sense or not. After each sentence, a to-be-remembered letter will be shown on the screen, which is followed by either another sentence-word combination or the final recall screen. The set size ranges from 3 to 7 items. At the end of each set of sentences, participants will be required to recall all the letters in the current set in order. There will be a total of 75 letters and 75 sentence judgements. The order of the set sizes will be at random for each participant. Participants' performance will be evaluated by calculating the total number of correctly recalled letter sets.

Intervention Type BEHAVIORAL

Barratt Impulsiveness Scale

The Barratt impulsiveness scale (BIS-11) will be used in the experiment to measure participants' trait impulsivity. Participants will be required to rate themselves on 30 items that are related to attention, motor, self-control, cognitive complexity, perseverance, and cognitive instability impulsiveness.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Native Dutch speakers
* Right-handed

Exclusion Criteria

* Current (or history of) psychiatric disorder (e.g., psychosis, mania, severe depressive disorder)
* Current (or history of) neurological disorder (e.g. m. Parkinson, epilepsy)
* Current (or history of) endocrine / metabolic disorder
* Current (or history of) cardiac or vascular disorder
* Current (or history of) blood illness (e.g. severe anaemia, porphyria)
* Current (or history of) stomach or gastrointestinal tract disease
* History of autonomic failure (e.g., vasovagal reflex syncope)
* Experience of irregular sleep-wake rhythm
* Current (or history of) obstructive respiratory disease
* Current (or history of) clinically significant renal or hepatic disease
* (Recent treatment of) glaucoma
* Current (or history of) drug addiction (e.g. opiate, (meth)amphetamine, lysergic acid diethylamide, cocaine, solvents or barbiturate) or alcohol dependence
* One first degree or two or more second degree family members with a recent treatment of sudden death or ventricular arrhythmia
* Problems swallowing or problems with the oesophagus
* Frequent experience of headrush (vertigo)
* Current experience of an acute serious infection
* First degree family member with schizophrenia or bipolar disorder
* Abnormal hearing or (uncorrected) vision
* Use of psychotropic medication or recreational drugs weekly or more over a period of more than three months in the last 6 months
* Cannabis usage for the last 6 months
* Strong smoking behaviour starting at more than 1 package of cigarettes per week
* Hypersensitivity for e.g. beta blockers or methylphenidate
* Uncontrolled hypertension, defined as diastolic blood pressure at rest \>95 mmHg or systolic blood pressure at rest \>180 mmHg
* Irregular sleep/wake rhythm (e.g. regular nightshifts or cross timeline travel)
* Possible pregnancy or breastfeeding/ inadequate anticonception (for women)
* Lactose intolerance (because the placebo pill will be a lactose product)
* Language related disabilities (e.g. dyslexia, stuttering)
* Daily intense physical training
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Max Planck Institute for Psycholinguistics

UNKNOWN

Sponsor Role collaborator

Radboud University Medical Center

OTHER

Sponsor Role collaborator

Donders Centre for Cognitive Neuroimaging

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Peter Hagoort, PhD

Role: PRINCIPAL_INVESTIGATOR

Donders Centre for Cognitive Neuroimaging

Locations

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Donders Institute for Brain, Cognition and Behaviour, Centre for Cognitive Neuroimaging

Nijmegen, Gelderland, Netherlands

Site Status

Countries

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Netherlands

Other Identifiers

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NL69700.091.19

Identifier Type: -

Identifier Source: org_study_id

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