Overview

The Effect of Regular Naltrexone Dosing on Disordered Gamblers

Status:
Recruiting
Trial end date:
2021-12-30
Target enrollment:
0
Participant gender:
All
Summary
This study examines the effect of regular naltrexone dosing on disordered gamblers. Gamblers will also be scanned pre- and post-treatment where we will investigate the functional changes to tasks designed to engage brain region associated with gambling and addiction. These changes will be correlated with treatment outcomes and urge scores.
Phase:
Phase 1
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
University of Calgary
Collaborator:
Alberta Health Services
Treatments:
Naltrexone
Criteria
Inclusion Criteria:

- 18-70 years of age.

- Provide written consent.

- Evidence of Disordered Gambling (DSM-V; American Psychiatric Association, 2013)

- Seeking treatment for disordered gambling, referrals, or responding to information
about the study presented in the media.

- Primarily Video Lottery Terminal gamblers (to standardize gamblers and as we are using
stimuli in the gambling stimuli task that is similar to video lottery terminals
displays so gamblers will be familiar with these images).

- Attendance at Alberta Health Service Evening Gambling Intensive Program (EGRIP) or
similar

- English speaking

Exclusion Criteria:

- Evidence of a current significant medical illness, or unmanaged psychiatric or
neurological disorder.

- Positive urine specimen to drugs of abuse.

- History of a traumatic brain injury or loss of consciousness (10 minutes or more).

- History of evidence of claustrophobia

- Left handed.

- Any condition or circumstance that prohibit imaging sessions such as metal implants.

- Contraindications to clinical doses of naltrexone.

- History or evidence of allergic reactions to naltrexone administration (i.e., rash,
itching/swelling, severe dizziness, or trouble breathing).

- Concurrent use of additional alcohol dependence medication e.g. disulfiram.

- Evidence of current illicit opioid use

- Use of medications containing opioids/opiates

- Uncorrected visual impairment

- Evidence of brain abnormalities from structural scans

- Evidence of heart, liver or kidney failure.

- Failure to attend weekly EGRIP counselling sessions or similar

- Pregnant

Other Requirements:

- If sexually active must use contraception

- Cannot make ovum or sperm donation during study and six-months thereafter