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Working memory training in children with neuropsychiatric disorders and mild to borderline intellectual disabilities

Working memory training in children with neuropsychiatric disorders and mild to borderline intellectual disabilities

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21467
Enrollment
50
Registered
2015-06-09
Start date
2016-01-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

In a double blind randomized controlled trial, two groups with 25 children will train 8 weeks, 4 days a week for an average of 35 minutes (5 exercises) each day. Parents, children and teachers will b

Sponsors

Karakter
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Children aged between 10 years/0 months and 13 years/11 months, known in psychiatric health care and/or special education. 2. Neuropsychiatric disorders (ADHD, ASD, or a combination of those two), classified by the DSM-IV/ DSM-5 (Diagnostic and Statistical Manual of Mental Disorders, 2000, 2013). 3. IQ score between 60 and 85. 4. Access to a PC with Windows Vista or Windows XP with internet connection and speakers at school

Exclusion criteria

Exclusion criteria: 1. Treatment at an inpatient or day treatment clinic. 2. Regular use of other medication than for ADHD or ASD . 4. If medication for ADHD/ASD is used and ‘room for improvement for ADHD symptoms’ is absent 3. Diagnosis of one or more of the following comorbid psychiatric disorders (checked by DISC-IV): - Major depression - Bipolar disorder - Psychotic disorder - Conduct disorder - Anxiety disorder - Neurological disorders (e.g. epilepsy) in the recent two years. - Cardiovascular disease currently or in the past. - Serious motor and/or perceptual handicap. - Participation in another clinical trial simultaneously. - Insufficient motivation to follow the training. - Medical illness which needs medical treatment.

Design outcomes

Primary

MeasureTime frame
The primary objective is to investigate the effect of a less intensive but prolonged Cogmed© RM working memory training with active personalized coaching and feedback in children with MBID and neuropsychiatric disorders, compared to a less intensive but prolonged RM Cogmed © working memory training without personalized (only general non-personalized coaching) coaching and feedback, on neurocognitive functioning measured with the span-board task.

Secondary

MeasureTime frame
Secondary, the effect of active personalized coaching will be investigated on various other neurocognitive functioning domains (working memory and executive functioning), academic achievements (arithmetic and reading) and behavioural problems and parenting style.

Contacts

Public ContactSammy L. Roording-Ragetlie

Karakter, cluster LVG Utrechtseweg 220

s.roording@karakter.com+31 (0)26 4002100

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)