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Effect on Fatigue of Light (Lux) Therapy in Patients With Cancer (EFFLUX)

Primary Purpose

Cancer

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
light therapy
Usual care
Sponsored by
Fondation Hôpital Saint-Joseph
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer focused on measuring fatigue, tiredness, luxo therapy, therapy by light

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Cancer histologically or cytologically confirmed (regardless of type)
  • Patient eligible for first-line chemotherapy
  • Life expectancy> 3 months
  • WHO PS ≤ 2
  • Age ≥ 18 years
  • Informed consent signed and dated
  • Affiliation to a social security scheme

Exclusion Criteria:

  • Macular degeneration
  • Diabetic retinopathy
  • Glaucoma
  • untreated cataract
  • Patient treated with vitamin D
  • Psychiatric disorders (bipolar disorder, paranoia, schizophrenia)
  • For patients with other comorbidities may indicate against-the practice of therapy: application specialist opinion (ophthalmologist or psychiatrist)

Sites / Locations

  • Groupe Hospitalier Paris Saint JosephRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Light therapy

usual care

Arm Description

Light therapy takes place in the patient's home the day following receipt of the equipment and for at least 7 days before the start of chemotherapy and according to current recommendations: daily exposure to a high intensity light (10,000 lux) in the morning at a time to be adapted to the patient according to his chronotype), for 30 minutes. Light therapy begins immediately after receipt of the luminometer. The total duration of daily outpatient therapy program is 6 months. A set of questionnaires evaluation of fatigue and quality of life will be given to the patient at the inclusion visit and at weeks 12 and 24. They will complete the same day or the day before, and / or before any chemotherapy. A follow-up visit will be performed 1 month after the end of therapy (week 28).

usual care in oncology: The patient will be taken care of according to local chemotherapy in routine care and the recommendations. A set of questionnaires evaluation of fatigue and quality of life will be given to the patient at baseline and at weeks 12 and 24. They will complete the same day or the day before, and / or chemotherapy before . A follow-up visit will be performed 1 month after the last visit (week 28). A set of questionnaires evaluation of fatigue and quality of life will be given to the patient and will complete the same day or the day before

Outcomes

Primary Outcome Measures

Assessment of change of Tiredness: PIPER Score
Tiredness: PIPER Score (main variable) (22 items targeted in 4 dimensions: behavioral tiredness / intensity, emotional, sensory and cognitive / mood)

Secondary Outcome Measures

Assessment of change of Quality of life (EORTC-QLQ-C30 SCORE)
Quality of life related to health: EORTC-QLQ-C30 (30 items targeted in 4 dimensions: the overall quality of life, fatigue, physical functioning and pain).
Assessment of change of Health General condition WHO SCORE
General condition: WHO
Assessment of change of Pain SCORE
Pain: BPI-Short Form (BPI-SF) and analgesic consumption
Assessment of change of Depression Scale
Depression / Anxiety: scale of depression and anxiety (HADS)
Assessment of change of slumber
Sleep: Pittsburgh questionnaire (PSQI)

Full Information

First Posted
August 23, 2016
Last Updated
May 4, 2023
Sponsor
Fondation Hôpital Saint-Joseph
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1. Study Identification

Unique Protocol Identification Number
NCT02879864
Brief Title
Effect on Fatigue of Light (Lux) Therapy in Patients With Cancer
Acronym
EFFLUX
Official Title
Effect on Fatigue of Light (Lux) Therapy in Patients With Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 20, 2019 (Actual)
Primary Completion Date
September 19, 2023 (Anticipated)
Study Completion Date
April 20, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondation Hôpital Saint-Joseph

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Fatigue is a symptom most commonly associated with the diagnosis of cancer. Fatigue often appears before the diagnosis of cancer, is increasing during treatment with chemotherapy and persists for years after treatment in more than 35% of patients. Fatigue is the earliest and most important symptom described by cancer patients. Its prevalence in cancer chemotherapy patients is between 70 and 100%. Fatigue is more common to cancer patients and to the general population or other types of patients. Typically described as a lack of energy associated with mental disorders, fatigue related to cancer can be extremely debilitating. The causes are many, mainly including the cancer itself, side effects due to treatment, sleeplessness due to pain, anxiety or depression. The cancer-related fatigue has a negative and significant direct impact on all aspects of the patient's quality of life, especially the physical, social and behavioral. Despite the availability of certain treatments and the advanced biomedical research, fatigue remains an inevitable consequence of cancer and its treatment. The therapeutic use of natural light in medicine dates back to the late nineteenth century. Its remarkable effect on the stimulation of the immune system and fight against infections caused the development of the first therapy techniques (also called luxthérapie) awarded in 1903 by the Nobel Prize in medicine and physiology. Light plays a fundamental role in the regulation of circadian rhythms and homeostatic. The mechanism of action passes through a path "non-visual" involving melanopsin ganglion cells located in the retina. Activation of the pineal gland (epiphysis) by melanopsin cells allows transduce information "shadow and light" in melatonin synthesis from serotonin. Today, the effectiveness of the therapy is well established for treating fatigue-related disorders such as chronic fatigue, seasonal depression or seasonal or non-certain sleep disorders and in which the melatonin metabolism is disturbed. Light therapy, by its mechanism of action, allows reprogramming "of the biological clock and improved synchronization of circadian rhythms.
Detailed Description
Hypotheses Some studies have shown an inverse relationship between cancer-related fatigue and the time of exposure to natural light for cancer patients. This association suggests the existence of a vicious circle of side effects of chemotherapy (physical fatigue and moral), itself causing a decrease in outdoor activity and therefore a reduction of the light exposure time natural. This results in a strengthening of the initial patient's state of fatigue. In an interesting way, vitamin D synthesized in large part due to light plays a cancer protective role], especially in the prevention and treatment of pancreatic cancer for example. Furthermore and paradoxical way, the disruption of circadian rhythms is correlated to the development and tumor progression in vitro, in vivo tumor growth and incidence of cancer in humans. Notoriously, the direct effect of light therapy on cancer-related fatigue has been little discussed in the literature. Data obtained from a small sample of patients indicate that light therapy improves quality of life by reducing fatigue in patients with breast cancer during chemotherapy. To date, There are no data on the effects of light therapy on cancer-related fatigue in general, patients treated with chemotherapy. The purpose of this pilot study is to evaluate the role of light therapy on cancer-related fatigue in patients during the 6 months following initiation of first-line chemotherapy. Primary objective To assess the effects of daily therapy on fatigue of patients with locally advanced or metastatic cancer treated with chemotherapy. secondary objective Evaluate the impact of daily light therapy on quality of life, pain, anxiety and depression, tolerance of chemotherapy and medico-economic benefits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer
Keywords
fatigue, tiredness, luxo therapy, therapy by light

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
152 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Light therapy
Arm Type
Experimental
Arm Description
Light therapy takes place in the patient's home the day following receipt of the equipment and for at least 7 days before the start of chemotherapy and according to current recommendations: daily exposure to a high intensity light (10,000 lux) in the morning at a time to be adapted to the patient according to his chronotype), for 30 minutes. Light therapy begins immediately after receipt of the luminometer. The total duration of daily outpatient therapy program is 6 months. A set of questionnaires evaluation of fatigue and quality of life will be given to the patient at the inclusion visit and at weeks 12 and 24. They will complete the same day or the day before, and / or before any chemotherapy. A follow-up visit will be performed 1 month after the end of therapy (week 28).
Arm Title
usual care
Arm Type
Active Comparator
Arm Description
usual care in oncology: The patient will be taken care of according to local chemotherapy in routine care and the recommendations. A set of questionnaires evaluation of fatigue and quality of life will be given to the patient at baseline and at weeks 12 and 24. They will complete the same day or the day before, and / or chemotherapy before . A follow-up visit will be performed 1 month after the last visit (week 28). A set of questionnaires evaluation of fatigue and quality of life will be given to the patient and will complete the same day or the day before
Intervention Type
Device
Intervention Name(s)
light therapy
Intervention Description
The light therapy, 6 month's program, is occurring at patient's home the day after device's reception and during at least 7 days before chemotherapy's beginning. The ambulatory light program is daily exposure to a high-intensity light (10,000 lux) in the morning, at a time adapted to the patient according to his chronotype for 30 minutes. The light source should be placed at eye level (distance of about 40 cm). A set of questionnaires evaluation of fatigue and quality of life will be given to the patient at baseline and at weeks 12 and 24, which will be completed the same day or the day before, and / or before any chemotherapy. These questionnaires will be also completed during the follow-up visit 1 month after the last visit (week 28).
Intervention Type
Device
Intervention Name(s)
Usual care
Intervention Description
The patient will be taken care of according to local chemotherapy in routine care and the recommendations. A set of questionnaires evaluation of fatigue and quality of life will be given to the patient at baseline and at weeks 12 and 24. They will complete the same day or the day before, and / or chemotherapy before. A follow-up visit will be performed 1 month after the last visit (week 28). A set of questionnaires evaluation of fatigue and quality of life will be given to the patient and will complete the same day or the day before.
Primary Outcome Measure Information:
Title
Assessment of change of Tiredness: PIPER Score
Description
Tiredness: PIPER Score (main variable) (22 items targeted in 4 dimensions: behavioral tiredness / intensity, emotional, sensory and cognitive / mood)
Time Frame
Day 1, week 12, week 24 and week 28
Secondary Outcome Measure Information:
Title
Assessment of change of Quality of life (EORTC-QLQ-C30 SCORE)
Description
Quality of life related to health: EORTC-QLQ-C30 (30 items targeted in 4 dimensions: the overall quality of life, fatigue, physical functioning and pain).
Time Frame
Day 1, week 12, week 24 and week 28
Title
Assessment of change of Health General condition WHO SCORE
Description
General condition: WHO
Time Frame
Day 1, week 12, week 24 and week 28
Title
Assessment of change of Pain SCORE
Description
Pain: BPI-Short Form (BPI-SF) and analgesic consumption
Time Frame
Day 1, week 12, week 24 and week 28
Title
Assessment of change of Depression Scale
Description
Depression / Anxiety: scale of depression and anxiety (HADS)
Time Frame
Day 1, week 12, week 24 and week 28
Title
Assessment of change of slumber
Description
Sleep: Pittsburgh questionnaire (PSQI)
Time Frame
Day 1, week 12, week 24 and week 28

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cancer histologically or cytologically confirmed (regardless of type) Patient eligible for first-line chemotherapy Life expectancy> 3 months WHO PS ≤ 2 Age ≥ 18 years Informed consent signed and dated Affiliation to a social security scheme Exclusion Criteria: Macular degeneration Diabetic retinopathy Glaucoma untreated cataract Patient treated with vitamin D Psychiatric disorders (bipolar disorder, paranoia, schizophrenia) For patients with other comorbidities may indicate against-the practice of therapy: application specialist opinion (ophthalmologist or psychiatrist)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lionel STAUDACHER, MD
Phone
+33 1 44 12 70 33
Email
lstaudacher@hpsj.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Helene BEAUSSIER, PhD, PharmD
Phone
+33 1 44 12 70 38
Email
hbeaussier@hpsj.fr
Facility Information:
Facility Name
Groupe Hospitalier Paris Saint Joseph
City
Paris
State/Province
Ile-de-France
ZIP/Postal Code
75014
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
BEAUSSIER Helene, PhD, PharmD
Phone
+33 1 44 12 70 38
Email
hbeaussier@hpsj.fr
First Name & Middle Initial & Last Name & Degree
Mohamed CHERIFI, PharmD
Phone
+33 1 44 12 70 84
Email
mcherifi@hpsj.fr

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Effect on Fatigue of Light (Lux) Therapy in Patients With Cancer

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