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Trial record 1 of 3 for:    Mohab Ibrahim
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The Effect of Light Therapy on Chronic Pain

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ClinicalTrials.gov Identifier: NCT03677206
Recruitment Status : Recruiting
First Posted : September 19, 2018
Last Update Posted : March 20, 2020
Sponsor:
Information provided by (Responsible Party):
Mohab Ibrahim, PhD MD, University of Arizona

Brief Summary:

Chronic pain is a major problem in the USA and the rest of the world, currently, all available pharmacological interventions carry with them significant side effects. Pain clinics are specially equipped to perform intentional pain procedures to manage pain. However, there remain groups of patients what neither benefit from pharmacological nor from interventional pain procedures. Other methods have shown only minor benefits such as hypnosis or cognitive behavioral therapy. Therefore, other techniques need to be investigated.

Light therapy has been shown to have significant biological effects on humans. For example, light therapy is used to manage depression. Several clinical trials have shown that certain wavelengths of light can improve wound healing, decrease temporomandibular joint dysfunction (TMJ) pain, and decrease fear of back pain. In these trials, light was directed at the site of pain. In an attempt to better understand the effect of different wavelengths of light, pre-clinical studies were conducted using rats. The investigators have shown green and blue Light emitting diode, (LED) light produced antinociception (analgesia) and reversed neuropathic pain associated with several models of chronic pain. The analgesic effect of light was completely blocked when rats had their eyes covered, this suggests that the analgesic effects seen are mainly due to systemic effect through the visual system.

Preliminary experiments on rats suggest that this effect is mediated through the endogenous opioids and cannabinoid system.

The investigators believe that LED light is a safe alternative to pharmacological intervention to manage pain by stimulating the endogenous endorphin and cannabinoid systems. The investigators initial target participants with history of HIV, chemotherapy induced peripheral neuropathy and fibromyalgia. Participants will be divided into 2 groups. The first group will be a control group exposed to white LED light. The second group will be exposed to green LED light, respectively. Participants will be asked to take LED light home and will be asked to set in a dark room for 2 hours daily for 3 months with their LED light on. At the end of the 3 months trial, the investigator will assess their pain intensity, analgesic use, and overall quality of life. The investigators hypothesis is that participants exposed to green and blue light will have less use of analgesics and will have better life quality.


Condition or disease Intervention/treatment Phase
Chronic Pain Device: Exposure to green LED light Device: Exposure to white LED light Not Applicable

Detailed Description:

During the initial visit, the investigator will collect several pieces of data from participants that are considered part of the routine care, if you are being seen in the clinic, this information will also be used for research purposes. Initially the investigator will ask participants to provide their age, gender, work status, disability status, type of work, whether a previous pain physician has evaluated or provided treatment in the past, if there is any ongoing litigation, a detailed description of the pain (burning, electrical, shooting…etc.) and its location. If the participants are being seen in the clinic for their normal care a detailed physical examination assessing the motor strength of the upper extremities, sensation to light touch and reflexes that is part of the standard of care will be provided for the participants. The participants will be asked to give a numerical value for their pain (a scale from 0-10 where 0 is no pain and 10 is the worst pain imagined). Two questionnaires will be provided for the participants to complete which are not standard of care. The first one is the EuroQol Group (EQ-5D) which provide an over assessment of the quality of life. The second is a medication log to document their analgesics use. If the participants are being evaluated via telephone call, the same questions will be conducted, but no physical exam will be provided.

The participants will be assigned to either a white, or green light group. The participants have 50% chance of being in either group. Once the participants are assigned a light group, the participants will be given a strip of Light emitting diode, (LED) light that correspond to their color group. The participants will be asked to take and use the LED strip in a dark room in their house every day for two hours to be exposed to the light, the participants will do this for 10 weeks. The study start date and the outcome assessment timeline will begin from the date of your first exposure to the assigned light. The participants will be asked to complete their weekly questionnaires and daily log, these will be given to the participants on their first clinic visit or sent to the participants if they live out of town. There will be several follow up appointments as detailed below. There is a chance the participants may be asked to cross over into a different group from the one the participants were assigned.

For the follow up clinic visit or phone call (Week 10), data similar to the information gathered at the initial visit will be collected. The description of the pain (burning, electrical, shooting…etc.) and its location will be reviewed. A physical examination assessing for pain and sensation to light touch that is part of the standard of care will be provided for the participants. At the end of the study, the participants will be asked to return the LED strip, their logs and questionnaires.

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 60 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Intervention Model Description: Initially, patients will receive White LED exposure, then they will be crossed over to Green LED exposure. The patients will not be told which one is the treatment and which one is the control.
Masking: Single (Investigator)
Primary Purpose: Supportive Care
Official Title: The Effect of Light Therapy on Chronic Pain
Actual Study Start Date : June 2016
Estimated Primary Completion Date : June 2020
Estimated Study Completion Date : December 2020

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Chronic Pain

Arm Intervention/treatment
Sham Comparator: Exposure to white LED light.
Subjects will exposed to white light provided to them, in their homes in a dark room for approximately 2 hours for 10 weeks
Device: Exposure to white LED light
Participants will be exposed to white LED strip lights in a dark room for 2 hours a day.

Experimental: Exposure to green LED light
Subjects will exposed to green light provided to them, in their homes in a dark room for approximately 2 hours for 10 weeks.
Device: Exposure to green LED light
Participants will be exposed to green LED strip lights in a dark room for 2 hours a day.

Cross over
Subject will be exposed to white light (sham) for 10 weeks, then have a wash out period for 2 weeks, then exposed to green light (experimental) for 10 weeks.
Device: Exposure to green LED light
Participants will be exposed to green LED strip lights in a dark room for 2 hours a day.

Device: Exposure to white LED light
Participants will be exposed to white LED strip lights in a dark room for 2 hours a day.




Primary Outcome Measures :
  1. For fibromyalgia pain. [ Time Frame: 10 - 22 weeks, depending on study arm ]
    reduction in the intensity of fibromyalgia pain as measured by the Numerical Pain Scale (NPS). The NPS has a value ranging from 0 to 10 out of a maximum of 10. ) means no pain. 10 means the most severe pain.

  2. For migraine headache pain. [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Reduction of number of headache days/month.


Secondary Outcome Measures :
  1. Health-related quality of life using Using the EQ-5D-5L (EuroQol five-dimension scale) [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Using the EQ-5D-5L (EuroQol five-dimension scale) assessment questionnaire, this questionnaire consists of five questions assessing the mobility, self care, ability to perform daily activity and overall functionality, pain discomfort, and anxiety are all scales that have 5 different answers to choose from consisting of one, to having no problems, to five being unable to. This will be a weekly questionnaire that will be assessed at the end of the study to check for improvements. Values of these assessments are scored, lower values are better.

  2. Visual Analog Score (VAS) [ Time Frame: 10 - 22 weeks, depending on study arm ]
    VAS, which is a scale of 0 -100, 100 meaning the best health you can imagine and 0 means the worst health you can imagine. This will be a weekly questionnaire that will be assessed at the end of the study to check for improvements.

  3. Pain Intensity [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Evaluating the percentage change in the pain intensity using the provided survey. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  4. Pain Episode Frequency [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Evaluating the percentage change in the pain episode frequency using the provided survey. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  5. Pain Episode Duration [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Evaluating the percentage change in the pain episode duration using the provided survey. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  6. Ability to Fall Asleep [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Evaluating the percentage change in the ability to fall asleep using the provided survey. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  7. Ability to Stay Asleep [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Evaluating the percentage change in the ability to stay asleep using the provided survey. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  8. Ability to Work [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Evaluating the percentage change in the ability to work using the provided survey. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  9. Ability to Excersize [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Evaluating the percentage change in the ability to excersize using the provided survey. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  10. Ability to Do Chores [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Evaluating the percentage change in the ability to do chores using the provided survey. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  11. For Migraine Headache pain [ Time Frame: 10 - 22 weeks, depending on study arm ]
    reduction in the perceived intensity of the headache phase of the migraine episodes. The scale ranges from 0-100%. This is a reported value by the patient which is subjective in nature.

  12. Decrease use of analgesics using self-reported survey. [ Time Frame: 10 - 22 weeks, depending on study arm ]
    Decrease in use of analgesics from baseline. Medications and doses of analgesics will be documented at baseline, during the study the subjects will document their daily analgesic usage, at the end of the study the analgesic usage will be compared to baseline usage.

  13. Short form McGill pain questionnaire [ Time Frame: 10 - 22 weeks, depending on study arm ]
    A survey to analyze the different types of pain using different descriptive (burning, sharp, shooting,...etc). The value ranges from 0-3. 0 means no pain. 3 means severe pain.

  14. Fibromyalgia Impact Questioner [ Time Frame: 10 - 22 weeks, depending on study arm ]
    A survey to evaluate the effects of Fibromyalgia. The scale ranges from 0-100. 0 means no impact. 100 means there is a severe negative impact secondary to fibromyalgia. The scale is subjective in nature

  15. Headache Impact Test (HIT-6) [ Time Frame: 10 - 22 weeks, depending on study arm ]
    A survey to evaluate the impact of headache. The value ranges from 36-78 points. 36 indicates no impact from headache. 78 indicates worst possible impact from headache.

  16. Migraine diary [ Time Frame: 10 - 22 weeks, depending on study arm ]
    A diary to document the severity of migraine

  17. Sleep Quality Assessment [ Time Frame: 10 - 22 weeks, depending on study arm ]
    A survey to analyze the quality of sleep. The value range from 0-21. 0 means the best quality of sleep. 21 means the worst quality of asleep. The survey is subjective in nature.

  18. O'Leary/Sant Voiding and Pain Indices [ Time Frame: 10 - 22 weeks, depending on study arm ]
    A subjective survey designed to investigate the impact of voiding on people with interstitial cystitis. The value ranges from 0-21. 0 means no negative impact. 21 means the worst possible impact.



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adults ages 18 - 80 able to understand English and comply with study protocol
  • Peripheral neuropathy from HIV or chemotherapy.
  • History of fibromyalgia
  • Headaches
  • Chronic Pain
  • 7-day average numeric pain score of 5/10 or greater at baseline evaluation

Exclusion Criteria:

  • Subjects receiving remuneration for their pain treatment
  • Subjects that are incarcerated
  • Subjects unable to read English and complete assessments
  • Addictive behavior, severe clinical depression, or psychotic features

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03677206


Contacts
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Contact: Mohab Ibrahim, PhD., MD (520) 874-7246 mibrahim@anesth.arizona.edu
Contact: Amol Patwardhan, PhD., MD (520) 874-7246 apatwardhan@anesth.arizona.edu

Locations
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United States, Arizona
Banner University Medical Center South Recruiting
Tucson, Arizona, United States, 85713
Contact: Mohab Ibrahim, PhD., MD    520-871-7246    mibrahim@anesth.arizona.edu   
Sponsors and Collaborators
University of Arizona
Investigators
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Principal Investigator: Mohab Ibrahim, PhD., MD University of Arizona
Publications of Results:
Other Publications:
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Responsible Party: Mohab Ibrahim, PhD MD, Director, Comprehensive Pain Management Clinic Associate Professor, Anesthesiology, University of Arizona
ClinicalTrials.gov Identifier: NCT03677206    
Other Study ID Numbers: 1604514512
First Posted: September 19, 2018    Key Record Dates
Last Update Posted: March 20, 2020
Last Verified: March 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Additional relevant MeSH terms:
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Chronic Pain
Pain
Neurologic Manifestations
Signs and Symptoms