Other Clinical Trial - Prevention of Seasonal Affective Disorder

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Mood Disorders
Seasonal Affective Disorder
Seasonal Affective Disorder (SAD)

See also
	Status	Clinical Trial	Phase
	Completed	`NCT01714050` - Cognitive-behavioral Therapy vs. Light Therapy for Preventing SAD Recurrence	N/A
	Completed	`NCT01784705` - Transcranial Bright Light Therapy in Seasonal Affective Disorder (SAD)	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT01714050 - Cognitive-behavioral Therapy vs. Light Therapy for Preventing SAD Recurrence

N/A

Completed

NCT01784705 - Transcranial Bright Light Therapy in Seasonal Affective Disorder (SAD)

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT00046449
Study type	Interventional
Source	GlaxoSmithKline
Contact
Status	Completed
Phase	Phase 3
Start date	September 2002
Completion date	June 2003

Prevention of Seasonal Affective Disorder

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms