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Behavioural Intervention
Cognitive Training for ADHD (CogtrainADHD Trial)
N/A
Waitlist Available
Led By Martin Soelch Chantal, PR
Research Sponsored by University of Fribourg
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change between two time points from baseline t1 to six week later t2 after cognitive training is assessed. follow up is assessed at 3 months t3 and 6 months t4
Awards & highlights
No Placebo-Only Group
Summary
This trial looks at how well cognitive training works for people with ADHD in Switzerland.
Eligible Conditions
- Attention Deficit Hyperactivity Disorder (ADHD)
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change between two time points from baseline t1 to six week later t2 after cognitive training is assessed. follow up is assessed at 3 months t3 and 6 months t4
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change between two time points from baseline t1 to six week later t2 after cognitive training is assessed. follow up is assessed at 3 months t3 and 6 months t4
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
ADHD symptoms for adults
ADHD symptoms for children
Secondary study objectives
Impulsivity
Memory
Neural activity
+2 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: experimental training group cognitive trainingExperimental Treatment1 Intervention
a multifactorial cognitive program that tackles working memory, attention, inhibition, planification and reasoning Exercice are realized at home using a computer 25 sessions of 30-45 minutes are realized five days per week during 5 weeks
Group II: control healthy participantsActive Control1 Intervention
Just a control group including healthy participants No intervention
Group III: active control group low-intensityActive Control1 Intervention
Low intensity version of the same cognitive training program Exercice are realized at home using a computer 25 sessions of 30-45 minutes are realized five days per week during 5 weeks
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Who is running the clinical trial?
University of FribourgLead Sponsor
12 Previous Clinical Trials
1,860 Total Patients Enrolled
Paris West University Nanterre La DéfenseOTHER
5 Previous Clinical Trials
1,138 Total Patients Enrolled
1 Trials studying Attention Deficit Hyperactivity Disorder (ADHD)
60 Patients Enrolled for Attention Deficit Hyperactivity Disorder (ADHD)
Martin Soelch Chantal, PRPrincipal InvestigatorUniversity of Fribourg
Amélie Dentz, Ph.DPrincipal InvestigatorUniversity of Fribourg
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: experimental training group cognitive training
- Group 2: control healthy participants
- Group 3: active control group low-intensity
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Attention Deficit Hyperactivity Disorder (ADHD) Patient Testimony for trial: Trial Name: NCT03799029 — N/A