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Metacognitive Intervention in Children and Adolescents With ADHD - MiA Study

Key facts

Who runs it
Insel Gruppe AG, University Hospital Bern
Where
Switzerland1 site in 1 countryChoose a country to see its sites
Trial code
Status
Completed
People taking part
42 people enrolled
Started
1 Aug 2025
Ended
18 Oct 2026
Type of study
Interventional, 2 groupsOne group gets an existing treatment, for comparison.
Treatments tested
  • Mio-Training
Record updated
12 November 2026

Who can take part

Age
8 years to 16 years
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

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Who can take part

  • Informed consent as documented by signature (see Informed Consent Form) of participants and / or one parent / legal guardian
  • Age 8-16 years
  • A diagnosis of ADHD (mild, moderate or severe)
  • Intelligence >85 (WISC-V short form)
  • German or french speaking
  • Willingness to perform the assessments without the medication (the study visits will take place without ADHD medication)

Who cannot take part

  • Any other instable neurological condition (e.g. epilepsy) that significantly impairs development
  • A severe psychiatric disease (e.g., eating disorder) or severe learning disability that significantly impairs development
  • Known or suspected non-compliance
  • Inability to follow the procedures of the study, e.g. due to language problems
  • Enrolment of the investigator, his/her family members, employees and other dependent persons

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

The aim of the MiA-Study is to address the current lack of effective treatment options to reduce cognitive and physical long-term problems in children and adolescents with Attention Deficit Hyperactivity Disorder (ADHD). Through the use of the Mio-Training, cognitive development will be strengthened and metacognitive thinking and awareness will increase.

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The MiA-Study is conducted additionally to the Mio-study to evaluate the effectiveness of the Mio-Training specifically within the ADHD population.

The Mio-Training for children and adolescence with ADHD includes a combination of cognitive and coordinative training tasks and prospective as well as retrospective metacognitive questions. In a randomized controlled trial, the Mio-Training will be analysed for its efficacy on metacognitive thinking and executive functions. In particular, the investigators are interested in factors that affect the efficacy of the training program such as compliance, age, sex or the severity of the ADHD. This study will give insight into the role of metacognition in cognitive performance and will foster the development of children and adolescents with ADHD in the long-term.

The 2 groups in the trial

  • Training groupExisting treatment, for comparison

    Training with Mio-Training for 5 weeks, three times per week.

    Treatment: Mio-Training

  • Control groupNo study treatment, for comparison

    Waiting control group. Participants may use the Mio-Training after completion of the last follow-up assessment.

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Record updated
12 November 2026