Last updated on February 2018

Psychoeducational Groups for Adults With ADHD

Brief description of study

This pilot study aims to assess patient satisfaction and preliminary efficacy of a psychoeducational group treatment, using a randomized waitlist-controlled trial, at two different outpatient clinics in mid-Norway. All participants will receive standard treatment during the intervention period. Assessment of client satisfaction (CSQ 8), general self-efficacy (GSE-6), ADHD-related quality of life (AAQoL) symptoms of ADHD (SCL-9; ASRS), and work participation will be conducted at time of recruitment prior to randomization (T0), pre- (T1), post-treatment (T2), with a 10 week follow-up.

Clinical Study Identifier: NCT03337425

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Bjørn Gjervan, Ph.D

Levanger Hospital, Nord-Tr ndelag Hospital Trust
Levanger, Norway
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Mariela Lara, phd

Tiller DPS - St. Olavs University Hospital
Trondheim, Norway
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