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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04757506
Other study ID # A02-B12-11B
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 9, 2012
Est. completion date March 15, 2013

Study information

Verified date February 2021
Source McGill University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to explore the effects of endogenous opioids on self-esteem and attentional bias toward social cues. This is achieved by administering the drug naltrexone, which temporarily decreases endogenous opioid activity.


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date March 15, 2013
Est. primary completion date March 15, 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - good physical health, - normal kidney and liver function results from within previous year Exclusion Criteria: - allergy to naltrexone - kidney or liver injury or disorder - bipolar, panic, or psychotic disorders - epilepsy - smoking more than 15 cigarettes per day - pregnancy - substance abuse - use of opioid analgesics, cocaine, recreational drugs (e.g., marijuana, LSD, ecstasy, etc.), or prescription medication (except oral contraceptives) within the past 10 days - use of over-the-counter drugs (e.g., analgesics, anti-inflammatories, sleeping aids, etc.) or alcohol within the past 24 hours - current experience of pain (e.g., headache) - use of anti-diarrheal medications in the 7 days prior to the study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Naltrexone
opioid receptor antagonist
Placebo


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
McGill University

Outcome

Type Measure Description Time frame Safety issue
Primary Self-esteem Self-reported levels of self-esteem assessed using the Rosenberg Self-Esteem Scale (Rosenberg, 1965). Possible scores range from 1 to 4. Higher scores indicate higher levels of self-esteem. Approximately 2 hours post placebo/drug administration
Primary Attentional bias scores for positive social cues on visual probe task Attentional bias was assessed using a Visual Probe Task. The investigators used a version of the VPT (DeWall, Maner, & Rouby, 2009) designed to assess attentional bias to cues of social acceptance (i.e., smiles). The outcome measure was attentional bias scores, calculated by subtracting mean reaction time scores on "valid" trials from mean reaction time on "invalid" trials. Higher positive scores indicate greater attentional bias to accepting faces. Approximately 2 hours post placebo/drug administration
Secondary Attentional bias scores for negative social cues on visual probe task Attentional bias was assessed using a Visual Probe Task. The investigators used a version of the VPT (DeWall, Maner, & Rouby, 2009) designed to assess attentional bias to cues of social rejection (i.e., disapproving faces). The outcome measure was attentional bias scores, calculated by subtracting mean reaction time scores on "valid" trials from mean reaction time on "invalid" trials. Higher positive scores indicate greater attentional bias to disapproving faces. Approximately 2 hours post placebo/drug administration
Secondary Reaction times on neutral-neutral trials on visual probe task Reaction times on neutral-neutral trials on the visual probe task were used to assess potential psychomotor side-effects of naltrexone Approximately 2 hours post placebo/drug administration
Secondary Self-liking For exploratory purposes, the self-esteem measure (Rosenberg, 1965) was split into two separate subscales examining feelings of self-liking and self-competence as in Tafarodi & Milne, 2002. Self-liking is thought to be more relationally derived and based on internalized perceptions of social approval. Scores range from 1 to 4, with higher scores indicating higher levels of self-liking. Approximately 2 hours post placebo/drug administration
Secondary Self-competence For exploratory purposes, the self-esteem measure (Rosenberg, 1965) was split into two separate subscales examining feelings of self-liking and self-competence as in Tafarodi & Milne, 2002. Self-competence is thought to be more autonomously derived and based on past goal pursuit. Scores range from 1 to 4, with higher scores indicating higher levels of self-competence. Approximately 2 hours post placebo/drug administration
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