Attention and Pain in Children With and Without Attention Deficit and/or Hyperactivity Disorder

NCT ID: NCT04766580

Last Updated: 2022-07-28

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 44 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-02-17
• Study Completion Date: 2023-06-30

Brief Summary

In Quebec, there has been an important increase of Attention Deficit Hyperactivity Disorder (ADHD) diagnosis since 2015. ADHD symptoms, related to behavioural and/or concentration difficulties, are very similar to other disorders symptoms, such as anxiety and depression, and have a significant impact on students' academic success and future life. Adults (parent, teacher, coach) expectations towards a child's abilities are consciously or unconsciously perceived by the child, influence his expectations of his own abilities, and thus his academic performance (Pygmalion effect). The child and his entourage's expectations are therefore a major factor to consider, especially in school-age children. According to ADHD studies, some brain areas involved in pain regulation and in attention cognitive abilities develop at a slower rate in children with ADHD than the other children.

Considering the deleterious consequences generated by the symptoms of this disorder, the research project aims to better understand the role of expectations in children with ADHD in a medical (pain) and school (attention abilities) context. It also aims to contribute to better understand the role of the brain on the expectations effect and ADHD. In this study, children expectations will be modulated while pain experiments and cognitive task will be realized by children with and without ADHD. Brain measures will also be assessed with advanced techniques.

Thus, we hope that the results will help improve intervention strategies in these contexts to ensure better support for children with ADHD, with a distant goal of contributing to the development of stronger tools for differential diagnostics.

Detailed Description

Attention Deficit with or without Hyperactivity Disorder (ADHD) is a neurodevelopmental disorder that affects 2 to 7% worldwide youth population and 6.2% of children aged 6 to 11 years in Quebec [1-3]. The main symptoms of this disorder are difficulties in regulating behaviour and/or concentration [4]. These difficulties have significant negative consequences in someone's life, particularly in terms of their academic success [5] and has significant negative consequences in the medical context, increasing accidents and mortality risk [6].

Children's academic performance can be modulated by the Pygmalion (or Rosenthal) effect, which refers to an improvement or decrease in an individual's performance depending on the degree of belief in his or her abilities on the part of an authority or the environment [7]. Thus, these beliefs have an influence on a person's expectations of his or her ability to do a task, and thus on final performance [8]. The expectations of an individual and his or her entourage is therefore a major factor to consider, especially in school-age children [9]. Expectations also play an important role in the placebo effect. Whereas a placebo is a treatment without any real influence on a particular condition (drug or therapeutic technique), the placebo effect is the perceived beneficial effect following this treatment. Furthermore, a placebo effect is almost always added to the beneficial effect of a treatment in different ways (for example, an analgesic effect could occur faster or in a shorter delay) and to different degrees [10]. The placebo effect is regularly studied and increasingly understood in the context of pain [11]. Although the perception of pain is influenced by placebo treatment, this effect is itself modulated by the expectations of the person in pain [12]. The dorsolateral prefrontal cortex (DLPFC) is an essential region for the placebo's mechanism of action [10]. In children with ADHD, there is a delay in the maturation of the cortical thickness of DLPFC between the ages of 7 and 10 years [13]. These differences in neuronal activity in the prefrontal region are associated with difficulties in attention control and inhibition in these children: inhibitory functions measured using transcranial magnetic stimulation (TMS) show a lower inhibition capacity in individuals with ADHD than without ADHD [14].

Considering the important consequences generated by the symptoms of this disorder, it is essential to better understand the role of the placebo/nocebo effect and expectations in children with ADHD in a medical (pain) and academic (attentional skills) context. Our goal is to better understand how this placebo/nocebo effects and expectations are associated with changes in the DLPFC and the inhibitory functions. This study also aims to better characterize the role of neurophysiological and neuroanatomical factors in these contexts, with the distant goal of contributing to the development of stronger tools for differential diagnostics.

Objectives (1) To compare the placebo/nocebo effect on pain and (2) on attention abilities in children with and without ADHD. (3) To determine if there is a relationship between the placebo/nocebo effect and neurophysiological (inhibitory mechanisms) and neuroanatomical (DLPFC) measures.

Assumptions

(1) Children with ADHD will have a weaker response to the placebo/nocebo effect on pain and (2) on attention abilities than children without ADHD (3) There is a moderate to strong association between the placebo/nocebo effect and neurophysiological/ neuroanatomical markers.

Methodology Data will be collected from 44 children, 22 with ADHD and 22 without ADHD.

At the first session, we will proceed with the experimentation of the placebo and nocebo effect on pain and on the ability to perform cognitive tasks. The experiment will be divided into two parts; a placebo part where the participant will have to take a "drug" (inactive; placebo) that improves cognitive abilities and pain tolerance for a short period of time, and a nocebo part where the participant will have to take a "drug" (inactive; nocebo) that decreases cognitive abilities and pain tolerance for a short period of time. The placebo/nocebo effect will be induced using an inactive capsule that "increases" or "reduces" (depending on the experimenter's discourse) general cognitive skills, as well as sensitivity and tolerance to pain. Following the administration of each capsule, we will proceed with the pain and attention experiments, all in a randomized order. Between the two parts of the experimentation, we will proceed to the questionnaire administration with the participant. Since all the steps are approximately 45 minutes in length, we will be able to plan a session with participants lasting between one and one and a half hours.

In the second session, we will perform the neurophysiological (inhibitory mechanisms) and neuroanatomical (DLPFC) measures. At the end of the visit, we will also proceed with a review of the study in order to disclose the information that was obscured during the project. An explanatory document containing this information and the participant's detailed participation will also be given to the parent and the child.

Analyses T-tests will be used to assess the effect of expectations on pain in children with ADHD compared to children without ADHD (Objective 1). The same analyses will be conducted to compare the effect of expectations on the ability to perform attentional cognitive tasks between the two groups (objective 2). For objective 3, simple regressions will first be used to determine whether there is an association between independent variables (neurophysiological and neuranatomical measures) and the effect of expectations on pain and cognitive tasks. Potentially predictive variables with a p-value ˂ 0.15 on the correlation test will be retained for the development of the multiple regression model. All possible models, and therefore all subsets of the variables retained in the previous step, will be considered. Statistical criteria (R2, adjusted R2 and Mallow's Cp) as well as a critical clinical judgment will allow us to decide on the best model. This final model will only include variables with a beta coefficient that is significantly non-zero at the alpha level of 0.05.

Non-parametric analyses will also be performed to determine if significant results can be obtained. In addition to providing preliminary results, this study will provide the statistical parameters (mean, standard deviation) required to calculate the sample size.

Contributions Research. This study could contribute to a better understanding of the role of expectations in children with ADHD, in a medical (pain) and academic (attentional skills) context. It will also allow us to better understand the role of DLPFC in the mechanism of the placebo/nocebo effect.

Clinic. As a result, it will be potentially possible to improve the intervention strategies to be implemented in order to ensure better support for children with ADHD, also in the medical (pain) and school (attentional skills) contexts. This study may also allow a better general understanding and evaluation of the disorder, and thus reduce prejudice towards children with ADHD.

Conditions

Attention Deficit Disorder With Hyperactivity; Placebo Effect; Nocebo Effect; Pain

Study Design

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

Study Groups

Children with ADHD group

The same protocol is used for both groups

Group Type: EXPERIMENTAL

Placebo and nocebo effect

Intervention Type: BEHAVIORAL

The intervention focuses on the speech and instructions given with each placebo (positive for the placebo effect and negative for the nocebo effect)

Children with no ADHD group

The same protocol is used for both groups

Group Type: ACTIVE_COMPARATOR

Placebo and nocebo effect

Intervention Type: BEHAVIORAL

The intervention focuses on the speech and instructions given with each placebo (positive for the placebo effect and negative for the nocebo effect)

Interventions

Placebo and nocebo effect

The intervention focuses on the speech and instructions given with each placebo (positive for the placebo effect and negative for the nocebo effect)

Intervention Type: BEHAVIORAL

Other Intervention Names

Pygmalion effect

Eligibility Criteria

Inclusion Criteria

• Child 8 or 9 years old
• ADHD diagnosis confirmed by a qualified health professional (for the ADHD group only).
• Understand French

Exclusion Criteria

• Other neurological problems other than ADHD
• Diagnosis of a psychological disorder
• Intellectual disability

• Minimum Eligible Age: 8 Years
• Maximum Eligible Age: 9 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Université de Sherbrooke

OTHER

Sponsor Role: lead

Responsible Party

Guillaume Léonard

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Guillaume guillaume.leonard2@usherbrooke.ca, pht., PhD

Role: PRINCIPAL_INVESTIGATOR

Université de Sherbrooke

Locations

Centre de recherche sur le vieillissement (CdRV)

Sherbrooke, Quebec, Canada

Site Status: RECRUITING

Countries

Canada

Central Contacts

Carmen-Édith Belleï-Rodriguez, ps.ed., MSc

Role: CONTACT

carmen-edith.bellei-rodriguez@usherbrooke.ca

+1 819-780-2220 ext. 45195

Guillaume Léonard, pht., PhD

Role: CONTACT

guillaume.leonard2@usherbrooke.ca

+1 819-780-2220 ext. 45246

Facility Contacts

Carmen-Édith Belleï-Rodriguez, ps.ed., MSc

Role: primary

carmen-edith.bellei-rodriguez@usherbrooke.ca

819-780-2220 ext. 45195

Guillaume Leonard, pht, Ph.D.

Role: backup

guillaume.leonard2@usherbrooke.ca

819-780-2220 ext. 45246

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Other Identifiers

2020-3357

Identifier Type: -

Identifier Source: org_study_id