Trial Outcomes & Findings for Brain Network Modulation and Alcohol Use (NCT NCT04828577)

NCT ID: NCT04828577

Last Updated: 2026-02-10

Results Overview

Participants were asked to move a neurofeedback dial to "alcohol" or "goal" directions. For the "alcohol" they were instructed to attempt to crave alcohol, and for the "goal" they were instructed to attempt to project themselves into their future goals. The outcome was measured by the mean correlation of the needle movement compared to the instructed needle movement.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

21 participants

Primary outcome timeframe

During the real time fMRI scan, approximately 1 hour (single session)

Results posted on

2026-02-10

Participant Flow

Participant milestones

Participant milestones
Measure
Real Time Neurofeedback
Real time neurofeedback will be based on a classifier of increasing or decreasing alcohol craving/demand fMRI patterns. Participants will try to modulate their brain patterns based on neurofeedback via a visual dial during an fMRI scan. Participants will be told they will be controlling the visual dial. Real Time Neurofeedback: Participants receive feedback from their own brain activity.
Overall Study
STARTED
21
Overall Study
COMPLETED
21
Overall Study
NOT COMPLETED
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Brain Network Modulation and Alcohol Use

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Real Time Neurofeedback
n=21 Participants
Real time neurofeedback will be based on a classifier of increasing or decreasing alcohol craving/demand fMRI patterns. Participants will try to modulate their brain patterns based on neurofeedback via a visual dial during an fMRI scan. Participants will be told they will be controlling the visual dial. Real Time Neurofeedback: Participants receive feedback from their own brain activity.
Age, Categorical
<=18 years
0 Participants
n=41 Participants
Age, Categorical
Between 18 and 65 years
21 Participants
n=41 Participants
Age, Categorical
>=65 years
0 Participants
n=41 Participants
Sex: Female, Male
Female
11 Participants
n=41 Participants
Sex: Female, Male
Male
10 Participants
n=41 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=41 Participants
Race (NIH/OMB)
Asian
1 Participants
n=41 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=41 Participants
Race (NIH/OMB)
Black or African American
3 Participants
n=41 Participants
Race (NIH/OMB)
White
16 Participants
n=41 Participants
Race (NIH/OMB)
More than one race
1 Participants
n=41 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
n=41 Participants

PRIMARY outcome

Timeframe: During the real time fMRI scan, approximately 1 hour (single session)

Participants were asked to move a neurofeedback dial to "alcohol" or "goal" directions. For the "alcohol" they were instructed to attempt to crave alcohol, and for the "goal" they were instructed to attempt to project themselves into their future goals. The outcome was measured by the mean correlation of the needle movement compared to the instructed needle movement.

Outcome measures

Outcome measures
Measure
Real Time Neurofeedback
n=21 Participants
Real time neurofeedback will be based on a classifier of increasing or decreasing alcohol craving/demand fMRI patterns. Participants will try to modulate their brain patterns based on neurofeedback via a visual dial during an fMRI scan. Participants will be told they will be controlling the visual dial. Real Time Neurofeedback: Participants receive feedback from their own brain activity.
Neurofeedback Control
0.061 correlation coefficient
Standard Deviation 0.190

Adverse Events

Real Time Neurofeedback

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Stephen LaConte

Virginia Tech

Phone: 5405262008

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place