Blue-blocking Glasses for Sleep Disorders in Child and Adolescent Psychiatry
NCT07433491 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2026-02-25
Summary
Sleep problems and regulation difficulties are frequent in the child and adolescent psychiatry population. Insomnia and delayed sleep-wake phase disorders (DSPWD) are highly prevalent, and risk factors for developing more severe illness courses and chronic disorders. Pharmacological treatments of sleep disorders dominate even for the youngest patients but are unsupported by long-term data on outcome and side effects. The majority of non-pharmacological treatment options are composite and resource demanding. The investigators will examine the effects and feasibility of the isolated intervention of evening/night use of blue-blocking glasses/real darkness as adjunctive treatment for insomnia and delayed sleep phase disorder in inpatient and outpatient settings for children and adolecents.
Conditions
- Insomnia
- Delayed Sleep Phase Disorder
- Hyperarousal
- Transdiagnostic Psychopathology
- Child and Adolescent Psychiatry
Interventions
- DEVICE
-
Blue-blocking glasses (BB-glasses) or real darkness from 9 p.m. to desired wake-up time + night mode setting on mobile phone
Blue-blocking glasses and night mode on mobile phoneBlue-blocking glasses (BB-glasses) or real darkness from 9 p.m. to desired wake-up time + application of dark mode setting on the participant's mobile phone (if not already in use) + registration of brightness on participant's mobile phone screen (%) + treatment as usual
- OTHER
-
Control
Application of dark mode setting on the participant's mobile phone (if not already in use) + registration of brightness on particpants's mobile phone screen (%) + Treatment as usual
Sponsors & Collaborators
-
University of Bergen
collaborator OTHER -
University of Oslo
collaborator OTHER -
University Hospital of North Norway
collaborator OTHER -
Helse Vest
collaborator OTHER -
Helse Fonna
lead OTHER
Principal Investigators
-
Tone Elise G Henriksen, MD PhD · Helse Fonna
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 12 Years
- Max Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-02-01
- Primary Completion
- 2027-06-01
- Completion
- 2027-06-01
Countries
- Norway
Study Locations
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