Research
Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital
Published

Methodological advantages and disadvantages of parallel and crossover randomised clinical trials on methylphenidate for attention deficit hyperactivity disorder: a systematic review and meta-analyses

Research output: Contribution to journalJournal articleResearchpeer-review

  1. Power estimations for non-primary outcomes in randomised clinical trials

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Physical demand at work and sick leave due to low back pain: a cross-sectional study

    Research output: Contribution to journalJournal articleResearchpeer-review

  1. Power estimations for non-primary outcomes in randomised clinical trials

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Glucocorticosteroids for people with alcoholic hepatitis

    Research output: Contribution to journalReviewResearchpeer-review

  3. Radix Sophorae flavescentis versus no intervention or placebo for chronic hepatitis B

    Research output: Contribution to journalReviewResearchpeer-review

  • Helle B Krogh
  • Ole Jakob Storebø
  • Erlend Faltinsen
  • Adnan Todorovac
  • Erica Ydedahl-Jensen
  • Frederik Løgstrup Magnusson
  • Mathilde Holmskov
  • Trine Gerner
  • Christian Gluud
  • Erik Simonsen
View graph of relations

OBJECTIVE: To assess the methodological advantages and disadvantages of parallel and crossover designs in randomised clinical trials on methylphenidate for children and adolescents with attention deficit hyperactivity disorder (ADHD).

DESIGN: Secondary analyses of a Cochrane systematic review.

SETTING AND PARTICIPANTS: We searched relevant databases up to March 2015 and included data from parallel and crossover randomised trials assessing children and adolescents up to 18 years with ADHD.

INTERVENTIONS: Methylphenidate compared with placebo or no-treatment interventions.

PRIMARY AND SECONDARY OUTCOMES: The primary outcomes were teacher-rated ADHD symptoms and serious adverse events. The secondary outcomes were non-serious adverse events.

RESULTS: We included 38 parallel trials (n=5111) and 147 crossover trials (n=7134). When comparing methylphenidate with placebo or no-treatment on ADHD symptoms, we found no differences between the end of parallel trials and the first-period from crossover trials (Χ²=1.06, df=1, p=0.30, I²=5.5%). We also found no differences when combining the end of first-period crossover trials with the end of parallel trials and comparing them to the end of last-period crossover trials (Χ²=3.25, df=1, p=0.07, I²=69.2%). We found no differences in serious and non-serious adverse events, and no risk of period and carryover effects. However, only two trials contributed data to the latter analyses.

CONCLUSIONS: Both parallel and crossover trials seem suitable for investigating methylphenidate in children and adolescents with ADHD, with comparable estimates on ADHD symptom severity and adverse events. However, parallel trials might still offer ethical and statistical advantages over crossover trials.

Original languageEnglish
JournalBMJ Open
Volume9
Issue number3
Pages (from-to)e026478
ISSN2044-6055
DOIs
Publication statusPublished - 30 Mar 2019

ID: 56915250