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N/A Completed N=14 Randomized Single-blind Device Feasibility

Feasibility of Bright Light Therapy on Fatigue, Sleep and Circadian Activity Rhythms in Lung Cancer Survivors

Fatigue · Sleep Disturbances · Circadian Dysregulation
Source: ClinicalTrials.gov NCT02954809 ↗
Enrolled (actual)
14
Serious AEs
0.0%
Results posted
May 2025
Primary outcomePrimary: Study Completion — 7; 5 Participants

Summary

The purpose of this study is to determine the feasibility of a morning bright light therapy intervention for fatigue, sleep disturbances, and circadian activity rhythms in lung cancer survivors.

Outcome Measures

OutcomeResultp-value
PRIMARY
Study Completion
7; 5

Eligibility Criteria

Inclusion Criteria

  • Stage I-III Non-small cell lung cancer survivors
  • Must be at >6-weeks and < 3 years post-surgical resection
  • Must have diagnosis fatigue and/or sleep disturbances

Exclusion Criteria

  • Individuals clinically unstable.
  • Mania, Bipolar disease or seizure disorder
  • Macular degeneration or glaucoma.
  • Currently receiving chemotherapy or radiation.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02954809). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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