The Use of Light Therapy for Managing Sleep Disturbances in Patients With Advanced Cancer

M.D. Anderson Cancer Center

Status and phase: Terminated; Phase 3; Phase 2

Conditions: Advanced Cancers

Treatments: Device: Red Light Litebook; Other: Dim Red Light Therapy; Behavioral: Questionnaires; Other: Bright Light Therapy; Device: Bright Light Litebook; Behavioral: Study Diaries

Study type: Interventional

Funder types: Other

Identifiers

NCT01193530

NCI-2012-01793 (Registry Identifier)

2009-0738

Details and patient eligibility

About

The goal of this research study is to learn if a type of light therapy can be used to help patients with advanced cancer who are having difficulty sleeping to sleep better.

Full description

Study Groups:

If you are found to be eligible to take part in this study, you will be randomly assigned (as in the flip of a coin) to one of two groups:

• Group 1 will receive one type of light therapy for 30 minutes every day for 14 days.
• Group 2 will receive a placebo light for 30 minutes every day for 14 days. The placebo light is not designed to have any effect on your sleep.

You will not know which group you are in. After 14 days, both groups will begin receiving the light therapy for another 14 days.

Litebook:

You will use a device called a Litebook to receive either the light therapy or the placebo light for 30 minutes, within 2 hours of waking up every day. The Litebook is about the size of a deck of cards. To use the Litebook, you will place it on a table within 2 feet of you while you are sitting down. The Litebook will either deliver the light therapy or the placebo light. You do not need to look directly into the Litebook and you can do usual activities such as eating or reading while you are using it. The study staff will teach you how to use the Litebook.

Study Diaries:

You will complete the following diaries at the end of each day of the 28-day study period:

• The light exposure diary about how much light you were exposed to.
• The sleep diary about your sleeping habits.

It should take about 5 minutes each day to make entries in the study diaries. You will return the diaries to the study staff at 2 weeks and 4 weeks.

You will also wear a watch that will measure your activity level for 24 hours a day while you are on study. You will return the watch to the study staff after you have completed the study.

Questionnaires:

You will complete a questionnaire about any symptoms you are having from the light therapy at the beginning of the study, at 1 week, at 2 weeks, and at 4 weeks. The questionnaire at 1 week can be done over the phone. It should take about 5 minutes to complete.

You will complete the following questionnaires at the beginning of the study, at 2 weeks, and at 4 weeks:

• The Edmonton Symptom Assessment Scale. You will rate 10 symptoms such as tiredness, shortness of breath, pain, and nausea.
• The FACIT-F questionnaire about how well you are able to perform the normal activities of daily living, your quality of life, and how tired you are.
• The HADS questionnaire about your mood.
• The Pittsburgh Sleep Quality Index about your sleep quality, how long you sleep, and any difficulties you are having when you are trying to sleep.

It should take about 25 minutes to complete all of the questionnaires.

Length of Study:

You will be on study for 28 days.

This is an investigational study. The use of light therapy in patients with difficulty sleeping is investigational. It is currently being used for research purposes only.

Up to 152 patients will take part in this study. All will be enrolled at M. D. Anderson.

Enrollment: 12 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Advanced cancer patients seen in Supportive Care outpatient clinic at M.D. Anderson Cancer Center, with average sleep disturbance >=4 out of 10 for at least one week
2. Age 18 or greater
3. Karnofsky performance status score of >=40 at time of inclusion into study
4. Agrees to return to MD Anderson Cancer Center (MDACC) for follow-up visits
5. English speaking

Exclusion criteria

1. Persons with congenital blindness and self-reported acquired blindness (independent of the cause) with no light perception
2. Patients with a history of retinal disease
3. Patients with a current diagnosis of major depression disorder or generalized anxiety disorder
4. Patients who have received light therapy in the past either as part of treatment for other disorders or as a study subject
5. Patients currently on amiodarone, thiazide diuretics or epidermal growth factor receptor (EGFR) inhibitors (erlotinib, gefitinib, cetuximab, panitumumab)
6. Patients who are currently receiving ultraviolet A light/ultraviolet B light (UVA/UVB) therapy or tanning sessions at salons
7. Patients with a diagnosis of obstructive sleep apnea or narcolepsy
8. Patients with >2 hours of direct exposure to outdoor natural light per day (light exposure diary -- screening).

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: Double Blind

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12 participants in 2 patient groups, including a placebo group

Bright Light Therapy

Experimental group

Description:

Daily Bright Light Therapy using Bright Light Litebook device for two 14 day periods.

Treatment:

Device: Bright Light Litebook

Behavioral: Study Diaries

Behavioral: Questionnaires

Other: Bright Light Therapy

Dim Red Light Therapy

Placebo Comparator group

Description:

Daily Dim Red Light Therapy (placebo) using control Red Light Litebook device for 14 days then proceed to the open label phase and receive daily bright light for 14 days.

Treatment:

Behavioral: Study Diaries

Other: Dim Red Light Therapy

Behavioral: Questionnaires

Device: Red Light Litebook