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Completed

NCT Number: NCT04340622

Efficacy And Safety Of An Innovative Treatment Of Opiate Use Disorders

Investigators will test, for safety and efficacy, a novel treatment for opiate addiction that applies a 4-minute treatment of intense near infra-red light to stimulate a side of the brain that the investigators determine to be healthier, more mature, and less traumatized. Investigators will compare an active and a sham treatment given twice weekly for 4-weeks. Investigators hope this will lead to a significant weapon in the battle against the opioid epidemic as well as lead to psychological and physiological insights into possible relations among trauma, cerebral laterality, and addiction.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

McLean Hospital, Belmont, Massachusetts, United States

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About this study

This project is to demonstrate that a novel treatment for opiate addiction is safe and far superior to a sham comparison treatment. The treatment is hoped to significantly aid in the battle against the opioid epidemic that is ravaging much of the country and the world. The treatment consists of using a 4-minute application of transcranial photobiomodulation, near infra-red mode, through a supra-luminous LED, to one side of the forehead over the brain hemisphere that we determine (through a proprietary test) to have a more positive emotional valence. Based on preliminary data, we anticipate that the treatment will be very effective in reducing drug cravings, anxiety, and depression as well as in reducing relapses. Aim I will offer twice-weekly treatments to two groups, active and sham, for 4-weeks and will look specifically for differences in opioid cravings, anxiety, depression, and opioid use. The investigators will evaluate participants weekly for safety and efficacy for 3-weeks post-treatment. In Aim II a highly-regarded product engineer will work with the company to design a marketable product that may have patentable elements.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • all patients must between the ages of 18 and 70
  • meet criterion for a history of Opioid Use Disorder (OUD) on a Diagnostic Interview.
  • have opioid cravings
  • Enrollment will be made without regard to gender or ethnicity.
  • Patients who are receiving treatment for OUD or other psychiatric disorders, either psychological or pharmacological treatments, may continue their treatment during the time of the study but will be asked to try not to alter their treatment from the onset of the experiment until its conclusion. The statistical analysis will include covariates for doses of buprenorphine and methadone and use of non-prescribed opioids

Exclusion criteria

  • past history of a psychotic disorder (including schizophrenia or schizoaffective disorder)
  • history of violent behavior
  • history of a past suicide gesture or attempt, a history of current suicidal ideation, *history of a neurological condition (e.g. epilepsy, traumatic brain injury, stroke), *pregnancy
  • current acute or chronic medical condition requiring a medication that has psychological side-effects.
  • impaired decision-making capacity in the judgment of the investigators.

Treatment and study plan

supra-luminous LED

Device

810 nm light-emitting diode for the delivery of 2.1 J/cm2 to the brain.

Other names: unilateral trancranial photobiomodulation, near-infrared mode

SHAM

Device

Light-emitting diode covered with aluminium foil

Primary outcomes

  1. Change in Opioid Craving Scale

    Time frame: One year

    a published 3 question scale of opioid cravings. Each question asks the patient to rate his opioid cravings at the present time from 0 (none) to 9 (extreme). We use the average of the scores of the 3 questions. A low score is best.

  2. Change in Opioid drug use

    Time frame: One year

    TimeLine FollowBack method, measures the daily amount of opioid drug use (mg's of pills or grams used) for the period between observations.

Secondary outcomes

  1. Change in Patient reports of opioid use by TimeLine FollowBack method

    Time frame: One year

    patient reports supported by urine drug screens and a drug hair test at the end of the study

Sponsors and collaborators

Lead sponsor

MindLight, LLC

Industry

Collaborators

  • Harvard Medical School (HMS and HSDM)
  • Mclean Hospital
  • National Institute on Drug Abuse (NIDA)

Registry information

Official study title

A Project to Test The Efficacy And Safety Of An Innovative Treatment Of Opiate Use Disorders

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Apr 9, 2020
Registry last updated
May 25, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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