Attention-deficit/hyperactivity disorder (ADHD)
Conditions
Interventions
A 3-week intervention of one of the following:
1A) Methylphenidate, 3 x 20 mg/day
1B) Placebo, 3 x 20mg/day
2A) Light Therapy, 30 minutes/day
2B) Waiting list
3A) Mel, 3 mg/day
3B) Placebo, 3 m
Sponsors
PsyQ Haaglanden
Kenniscentrum ADHD bij volwassenen
Eligibility
Inclusion criteria
Inclusion criteria: Patient group and control group: Age 18 to 40 years old. Patient group: Diagnosis of ADHD.
Exclusion criteria
Exclusion criteria: Patient group and control group: Severe psychiatric comorbidity; substance abuse; contraindication for the intervention. Control group: ADHD; use of stimulant medication.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The change in Post-Illumination Pupil Response (PIPR). | — |
Secondary
| Measure | Time frame |
|---|---|
| - A change in refractive error test for myopia (nearsightedness), hyperopia (farsightedness), astigmatism (cylindrical error), presbyopia (focus difficulty), and strabismus (alignedness of the eyes); - A change in colour discrimination ability; - A change in oculomotor functioning; - A change in perimetry score (visual field); - A change in the self-reported oversensitivity to light. - A change in the self-reported ADHD symptoms on the ADHD Rating Scale (ADHD-RS); - A change in the performance on the QbTest, which measures ADHD symptoms objectively; - A change in Dim-Light Melatonin Onset (DLMO); - A change in chronotype as measured by the Munich Chronotype Questionnaire (MCTQ); - A change in chronotype as measured by the Morningness-Eveningness Questionnaire (MEQ); - A change in fatigue as measured by the Multidimensional Assessment of Fatigue (MAF); - A change on the Seasonal Pattern Assessment Questionnaire (SPAQ). | — |
Contacts
Public ContactDenise Bijlenga
PsyQ Psycho-Medical Programs, Expertise Center Adult ADHD, The Hague
Outcome results
None listed