Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED NA

30-Minute Light Exposure for the Treatment of Seasonal Affective Disorder

NCT01462305 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to evaluate the effect of light therapy using a narrow 467nm light compared to a 580nm light in subjects with Seasonal Affective Disorder (SAD). It is hypothesized that the 467nm light will improve the symptoms of SAD better than the 580nm light.

Interventions

  • DEVICE Control
  • DEVICE goLITE

Study Locations (4)

Massachusetts

  • McLean Hospital — Belmont
  • Brigham & Women's Hospital — Boston

Minnesota

  • University of Minnesota — Minneapolis

Ohio

  • Community Research Management Associates — Cincinnati

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2012-01-06
Est. Completion 2012-04-02
Phase NA

Sponsor

Philips Respironics

9 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01462305

The ClinicalTrials.gov registry entry for NCT01462305 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 35 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Philips Respironics, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Seasonal Affective Disorder appearing as the primary indexed condition, and to 2 interventions — of which Control is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01462305 reports 4 study locations spanning 3 distinct geographic areas — top geographies include Massachusetts, Minnesota, Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01462305 about?

NCT01462305 is a clinical study titled "30-Minute Light Exposure for the Treatment of Seasonal Affective Disorder". The primary objective of this study is to evaluate the effect of light therapy using a narrow 467nm light compared to a 580nm light in subjects with Seasonal Affective Disorder (SAD). It is hypothesized that the 467nm light will improve the symptoms of SAD better than the 580nm light.

What is the current status of trial NCT01462305?

This trial is currently completed. It is a NA study. The enrollment target is 35 participants. The study started on 2012-01-06. Estimated completion is 2012-04-02.

What conditions does trial NCT01462305 study?

This clinical trial studies the following conditions: Seasonal Affective Disorder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01462305?

The interventions under investigation include: Control (DEVICE), goLITE (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01462305?

This trial is sponsored by Philips Respironics, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01462305 being conducted?

This trial has 4 study locations across Massachusetts, Minnesota, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial