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Behavioural Intervention
Bright Light Therapy for Fatigue and Sleep Disorders in Lung Cancer Survivors
N/A
Waitlist Available
Research Sponsored by State University of New York at Buffalo
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Must have diagnosis fatigue and/or sleep disturbances
Stage I-III Non-small cell lung cancer survivors
Must not have
Mania, Bipolar disease or seizure disorder
Currently receiving chemotherapy or radiation
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 5 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial will study the effects of morning bright light therapy on fatigue, sleep, and daily activity patterns in people who have survived lung cancer.
Who is the study for?
This trial is for Stage I-III non-small cell lung cancer survivors who are 6 weeks to 3 years post-surgery and experiencing fatigue or sleep disturbances. It's not suitable for those who are clinically unstable, have bipolar disorder, seizure disorders, macular degeneration, glaucoma, or currently undergoing chemotherapy or radiation.
What is being tested?
The study is testing the effectiveness of morning bright light therapy versus dim light in improving fatigue levels, sleep quality, and circadian activity rhythms among lung cancer survivors.
What are the potential side effects?
While the trial does not mention specific side effects of bright light therapy, common ones may include eyestrain, headache or agitation. Dim light is considered a control with no expected active side effects.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I experience fatigue or have trouble sleeping.
Select...
I am a survivor of stage I-III non-small cell lung cancer.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have mania, bipolar disorder, or a seizure disorder.
Select...
I am currently undergoing chemotherapy or radiation.
Select...
I have macular degeneration or glaucoma.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Body Weight Changes
Change in fatigue symptoms with Fatigue Severity Index from pre-test to post-test
Change in sleep quality with the Pittsburgh Sleep Quality Index from pre-test to post-test
+1 moreSecondary study objectives
Assessement of chronotype with the Morningness versus Eveningness Questionnaire
Assessment of Environmental light with actigraphy (Actiwatch Spectrum Respironics)
Changes in Quality of Life with theFunctional Assessment of Cancer Therapy - Lung
Other study objectives
Assessment of Visual acuity with the Snellen visual acuity chart
Daytime Somnolence
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: ExperimentalExperimental Treatment1 Intervention
Exposure to morning bright light therapy delivered with Green-Blue Re-Timer glasses for 30 minutes in the morning during one week.
Group II: Attention ControlActive Control1 Intervention
Exposure to dim light delivered with Red-Yellow Re-Timer glasses for 30 minutes in the morning during one week.
Find a Location
Who is running the clinical trial?
State University of New York at BuffaloLead Sponsor
268 Previous Clinical Trials
51,596 Total Patients Enrolled
5 Trials studying Fatigue
110 Patients Enrolled for Fatigue
Oncology Nursing SocietyOTHER
10 Previous Clinical Trials
500 Total Patients Enrolled
1 Trials studying Fatigue
45 Patients Enrolled for Fatigue
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I have mania, bipolar disorder, or a seizure disorder.I experience fatigue or have trouble sleeping.I am currently undergoing chemotherapy or radiation.I have macular degeneration or glaucoma.I am a survivor of stage I-III non-small cell lung cancer.I had surgery between 6 weeks and 3 years ago.
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Research Study Groups:
This trial has the following groups:- Group 1: Experimental
- Group 2: Attention Control