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Transcranial Bright Light Therapy in Seasonal Affective Disorder (SAD)

Transcranial Bright Light Therapy in Seasonal Affective Disorder (SAD)- a Randomized Placebo-controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01784705
Acronym
SAD3
Enrollment
60
Registered
2013-02-06
Start date
2013-01-31
Completion date
2013-03-31
Last updated
2013-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Seasonal Affective Disorder (SAD)

Brief summary

Bright light therapy (BLT) has been found to be effective in treatment of seasonal affective disorder (SAD). The mechanism of action of conventional BLT in the treatment of SAD is under debate. Recently, transcranial bright light (TBL) via ear canals has been proved to modulate the neural networks of the human brain and improve cognitive performance in healthy subjects. Moreover, TBL has been found to alleviate symptoms of SAD in open trial. In this case the investigators will study the effect of transcranial bright light treatment via ear canals on depressive and anxiety symptoms in patients suffering from SAD in randomized controlled double-blind study design.

Interventions

The bright light treatment was given transcranially via ear canals by using bright light device. The bright light was produced using two light-emitting diodes (LEDs). The bright light was transmitted into both ear canals by an optical fibre. Daily 12 minutes TBL was taken at home during forenoon.

DEVICETranscranial placebo treatment

The placebo treatment was given transcranially via ear canals by placebo device. Daily 12 minutes placebo treatment was taken at home during forenoon.

Sponsors

University of Oulu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* patient has (according to the Diagnostic and Statistical Manual of Mental Disorders, fourth edition, text revision \[DSM-IV-TR\]) a Major depression, recurrent episode, seasonal pattern * Structured Interview Guide for the Hamilton Depression Rating Scale - Seasonal Affective Disorder Version Self Rating Version (SIGH-SAD-SR) score ≥ 16 * patient is over 18 years and under 66 years * patient can read and understand the subject information sheet * patient has signed the informed consent form * patient is not pregnant

Exclusion criteria

* patient has a lifetime psychotic disorder * patient has a bipolar disorder * patient has alcohol or some other substance use dependence or misuse * patient has some unstable somatic disorder * patient uses some psychotropic agencies * patient is, in the opinion of the investigator, unsuitable for any reason * patient is a member of the site personnel or their immediate families * patient has administered bright light therapy via ear canals during the current episode

Design outcomes

Primary

MeasureTime frameDescription
Structured Interview Guide for the Hamilton Depression Rating Scale - Seasonal Affective Disorder Version Self Rating Version, total score ≤9At the end of the four week study periodRemission, i.e., Structured Interview Guide for the Hamilton Depression Rating Scale - Seasonal Affective Disorder Version Self Rating Version total score ≤ 9

Secondary

MeasureTime frameDescription
Beck Depression Inventory-II, total score <=10At the end of the four week study periodRemission, i.e.,Beck Depression Inventory-II, total score \<=10
State Trait Anxiety Inventory -Y2, total scoreAt the end of the four week study period
Trail- making test (TMT-A and TMT-B),total timeAt the end of the four weeks study period

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026