Attention Deficit Hyperactivity Disorder (ADHD) Clinical Trial
Official title:
Cognitive Training in Children With Attention Deficit Hyperactivity Disorder (ADHD)
ADHD is associated with cognitive deficit. Therefore, cognitive training is often proposed as
an intervention for ADHD that targets cognitive deficits, with specific exercises through
intensive training sessions. This intervention is based on principles of brain plasticity and
cerebral functional reorganizations.
Working memory deficits constitute a key impairment in ADHD. That is why, Cogmed working
memory training is the most commonly used and studied cognitive training program in clinical
practice and research. It is clear from most studies that Cogmed training program increases
working memory in ADHD. However, transfer of learning is not demonstrated on: other cognitive
functions that are not targeted by the program, on ADHD symptoms, nor on academic
achievement.
In addition to this type of intervention multi-factorial program targeting different
cognitive function as Presco also exist but have been less studied.
To address these challenges, this study will follow a randomized and controlled design.
The main objective of this study is to examine the impact of cognitive training in comparison
with a control waiting-list group among children with ADHD on:
1. ADHD symptoms,
2. cognitive functioning,
3. attentional capacities
4. academic achievement.
The second objective is to compare two types of cognitive training a unifactorial program
Cogmed targeting working memory and a multifactorial Presco focusing on different cognitive
functions affected by ADHD.
Long-term effects are examined six months after training. Participants (n=90) will be
randomly assigned to the two experimental group (Cogmed or Presco) or to the control group
waiting list. Participants will be evaluated three time (time 1) just before the
intervention, (time 2) six weeks after the first evaluation, immediately after the
intervention and (time 3) six months after the intervention.
Attention-Deficit Hyperactivity Disorder (ADHD) is a chronic developmental disorder
characterized by symptoms of inattention, impulsivity and hyperactivity that do not
correspond to the child's developmental level (American Psychiatric Association, 2013). For a
diagnosis to be confirmed, symptoms must be present before age 12 and must be observed in at
least to two domains of functioning, such as school, work, social interactions and family
life (American Psychiatric Association, 2013).
ADHD is one of the most common neurobehavioral disorder with a prevalence estimated at about
5-7% for school-age children (Psychiatric Association, 2013).
ADHD alters family, social and academic functioning as well as one's professional life.
Results from studies indicated that working memory and inhibition are often altered in ADHD
in childhood and persist into adulthood.
Pharmacological treatments of ADHD mostly include psychostimulants (Amphetamine and
Methylphenidate) and non-stimulants (Atomoxetine, Clonidine, Guanfacine). Stimulants and
no-stimulants are effective in managing ADHD symptoms.
However, these treatments present some limitation. For instance, comorbid disorders reduce
stimulants efficacy in ADHD. Further, long-term effects over the year of stimulant are not
yet known. Stimulants may cause side effects on sleep, hunger and growth. That is why some
parents are reluctant to let their children take stimulants.
Currently, clinical guidelines recommend non-pharmacological interventions in conjunction
with medication for the treatment of ADHD.
The above-mentioned limitations to the use of medication stress the importance of developing
non-pharmacological approaches. Cognitive training is one type of non-pharmacological
intervention used in ADHD.
This intervention consists in improving cognitive deficits through specific exercises during
intensive training session. A growing number of studies examined the impact of cognitive
training in ADHD.
Cognitive training is based on principles of brain plasticity with the aim to train cognitive
function and to improve cognitive deficits in ADHD. According to these authors, during
training changes occur in neural connection associated to ADHD. This modification allows far
transfers to cognitive function not targeted by the program, to ADHD symptoms and academic
performances.
Results from a meta-analysis indicated that 68% of 25 studies examining ADHD and cognitive
training focus on working memory. These authors specify that Cogmed Working Memory Training
is currently the most used and studied program. Indeed, this program is available in 25
countries and used by 150 clinical practitioners (http://www.cogmed.com).
Currently, one meta-analysis including seven studies examines Cogmed Working Memory Training
program effects in ADHD. Results indicated that the impact of Cogmed on cognitive
functioning, ADHD symptoms and academic performance remains controversial.
Cogmed is an unifactorial program targeting working memory. In addition to this type of
intervention multi-factorial program targeting different cognitive function as Presco also
exist but has been less studied.
Objectives To address these challenges, this study will follow a randomized and controlled
design.
The main objective of this study is to examine the impact of cognitive training in comparison
with a control group among children with ADHD on:
1. ADHD symptoms,
2. cognitive functioning,
3. attentional capacities
4. academic achievement.
The second objective is to compare two types of cognitive training a unifactorial program
Cogmed targeting working memory and a multifactorial Presco focusing on different cognitive
functions affected by ADHD.
Long-term effects are examined six months after training. Procedure Participants (n=90) will
be randomly assigned to three groups.
1. Cogmed® : working memory training (unifactorial)
2. Presco® : different cognitive function are trained (multifactorial)
3. Control ( waiting list) Participants will be evaluated three time (time 1) just before
the intervention, (time 2) six weeks after the first evaluation, immediately after the
intervention and (time 3) six months after the intervention.
For Cogmed and Presco participants will train the same time. Before beginning the program an
appointment of one hour will be organized to present the program.
Participants will train at home during 25 sessions (about 30-45 minutes each) over a maximum
of 5-6 weeks.
A coach will call the participant one a week to verify program adherence. The coach will
verify participant results on internet before calling.
Cogmed working memory training CogMed® (RoboMemo,Cognitive Medical Systems AB, Stockholm)
version for children will be used in this program. Twelve exercises target verbal and
visio-spatial working memory. Difficulty is adjusted depending on participant performance`s
The program PRESCO® (Program in Cognitive Stimulation and rehabilitation ) comprises 40
exercises targeting: verbal and visio spatial working memory, attention capacities,
reasoning, executive functioning , language and mental imagery. Only exercises targeting
verbal, visual spatial working memory, and attentional capacities altered in ADHD are used in
this present study. Difficulty is adjusted depending on the participant performances.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03260205 -
Safety and Efficacy Study in Preschool Children Aged 4-5 Years With Attention-deficit/Hyperactivity Disorder (ADHD)
|
Phase 3 | |
Withdrawn |
NCT03546400 -
Safety, Tolerability and PK Study of Methylphenidate HCl ERCT in 4-5 Year Old Children With ADHD.
|
Phase 4 | |
Completed |
NCT02917109 -
LearningRx Cognitive Training for ADHD
|
N/A | |
Completed |
NCT02248948 -
Superiority of Omega-3 Versus Placebo on the Improvement of ADHD in Children
|
N/A | |
Recruiting |
NCT01750307 -
The Relationship of Essential Fatty Acids to Adult ADHD: The OCEAN Study (Oils and Cognitive Effects in Adult ADHD Neurodevelopment)
|
N/A | |
Recruiting |
NCT06170996 -
Internet-Assisted Behavioral Parent Training Intervention for Children With Attention Deficit Hyperactivity Disorder
|
N/A | |
Completed |
NCT00735371 -
Efficacy and Safety of Lisdexamfetamine Dimesylate (LDX) in Adolescents With Attention-Deficit/Hyperactivity Disorder (ADHD)
|
Phase 3 | |
Withdrawn |
NCT03580005 -
A 6-week Study to Evaluate the Safety and Efficacy of Quillichew ERCT in 4-5 Year Old Children With ADHD.
|
Phase 4 | |
Completed |
NCT02578030 -
Pharmacokinetic Study in Children and Adolescents Aged 6 to 17 Years Who Have Been Diagnosed With ADHD
|
Phase 1 | |
Completed |
NCT02574273 -
Pilot Trial of a Social Skills Group Treatment (Secret Agent Society Program)
|
N/A | |
Completed |
NCT02257216 -
Vayarin® Medical Food Study for Adults With Attention Deficit Hyperactivity Disorder (ADHD)
|
N/A | |
Recruiting |
NCT04943796 -
A Study to Learn About the Occurrence of ADHD in Adults With Mental Conditions and Their Quality of Life
|
||
Recruiting |
NCT04634006 -
Home-Based tDCS in Children With ADHD: A Randomized, Sham-Controlled tDCS and fNIRS Study
|
N/A | |
Active, not recruiting |
NCT02908802 -
Probiotic Supplement as Treatment for Students With ADHD
|
N/A | |
Completed |
NCT02604407 -
Safety and Efficacy Study of SHP465 in Adults Aged 18-55 Years With Attention-deficit/ Hyperactivity Disorder (ADHD)
|
Phase 3 | |
Completed |
NCT05870605 -
Drug Use Study With Intuniv® in European Countries
|
||
Terminated |
NCT03481959 -
Effectiveness of Methylphenidate Late Formula to Reduce Cannabis Use in Young Cannabis-Related Patients and Attention Deficit Disorder Hyperactivity
|
Phase 3 | |
Terminated |
NCT03638466 -
Exploratory fMRI Study on the Treatment for Impulsive Aggression in Children With Attention-Deficit/Hyperactivity Disorder
|
Phase 2 | |
Completed |
NCT03709940 -
Brain Connectivity in Attention Deficit Hyperactivity Disorder (ADHD)
|
N/A | |
Completed |
NCT02795637 -
Study of the What the Body Does to the Drug in Subjects With Mild, Moderate, and Severe Liver Dysfunction
|
Phase 1 |