Executive control training for adolescents with ADHD: Study protocol for a randomised controlled trial

被引:0
作者
Dyresen, Agnete [1 ,2 ,6 ]
Stubberud, Jan [1 ,3 ]
Fjermestad, Krister Westlye [1 ,4 ]
Haugen, Ingvild [5 ]
Oie, Merete Glenne [1 ,5 ]
机构
[1] Univ Oslo, Dept Psychol, Oslo, Norway
[2] Lovisenberg Diaconal Hosp, Nic Waals Inst, Oslo, Norway
[3] Lovisenberg Diaconal Hosp, Dept Res, Oslo, Norway
[4] Frambu Resource Ctr Rare Disorders, Siggerud, Norway
[5] Innlandet Hosp Trust, Brumunddal, Norway
[6] Univ Oslo, Dept Psychol, PB 1094, NO-0317 Oslo, Norway
关键词
ADHD; Neurodevelopmental disorder; Executive functions; Goal management training; Randomized control trial; Trial protocol; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; DEFICIT HYPERACTIVITY DISORDER; CHILDREN; MANAGEMENT; IMPAIRMENT; VALIDATION; THERAPY; RATINGS; ADULTS;
D O I
10.1016/j.cct.2023.107404
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Attention-Deficit/Hyperactivity Disorder (ADHD) is one of the most prevalent neurodevelopmental conditions diagnosed during childhood and adolescence. In addition to the commonly observed symptoms of inattention, hyperactivity, and impulsivity, individuals with ADHD often experience impairments in executive functions (EFs). Goal management training (GMT) is a cognitive remediation intervention targeting EFs, with empirical support from studies with adult populations, including ADHD. The objective of the upcoming trial is to assess the effectiveness of GMT for adolescents with ADHD. Methods: This pre-registered protocol outlines a multi-centre randomised controlled trial (RCT) comparing GMT to treatment as usual (TAU) to improve EFs. We aim to recruit 120 participants, aged 12 to 18 years, recently diagnosed with ADHD. Participants will be randomly allocated to the group-based GMT intervention in addition to TAU, or the TAU condition, through block randomisation with site stratification. GMT will be delivered in groups of four to six participants, with weekly two-hour sessions for seven weeks, complemented by separate parent and teacher sessions. TAU is standard community mental health treatment. The primary outcome measure will be parent-reported EF assessed with the Behaviour Rating Inventory of Executive Function 2 (BRIEF-2). Secondary outcomes will include ADHD symptom measures, social functioning, quality of life, and neuropsychological tests (attention span, inhibition, working memory, and visuo-motor speed). The outcome assessments will be conducted at baseline, 12 weeks, 12 months, and 24 months post-treatment. Conclusion: The study findings will contribute to determine the effectiveness of a non-pharmacological ADHD treatment, including outcome trajectories up to 24 months post-treatment.
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