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Can Exercise Rewire the Brain Addiction Circuitry?

Can Exercise Rewire the Brain Addiction Circuitry? A Randomized Trial of Exercise and Binge Drinking

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06317753
Acronym
REWIRED
Enrollment
60
Registered
2024-03-19
Start date
2026-01-31
Completion date
2027-12-31
Last updated
2025-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Exercise

Keywords

Addiction circuitry, Binge drinking, Neuroimaging

Brief summary

The aim of the present study is to apply neuroimaging techniques to investigate how physical exercise may influence the addiction circuitry, ultimately reducing alcohol consumption and craving in youth binge drinkers. This proposal will advance knowledge on how exercise may modulate the neurocircuitry of addiction. Uncovering the neurobiological mechanisms underlying the interactive neural effects of exercise and alcohol intake may provide additional scientific insights for the development of preventive and intervention programs for youth BD and AUD.

Detailed description

The proposed research plan focuses on the identification of changes in the structural and functional brain parameters (e.g. volume, brain activity), in response to a physical exercise (PE) protocol, on the neurocircuitry of addiction, after a 4 month-intervention program in college binge drinkers (BDs). The main objectives of this proposal are: O1) to evaluate the potential benefits of PE on the brain structure and function, particularly in the neurocircuitry of addiction, in a sample of Portuguese college students with a binge drinking pattern of alcohol use; and O2) to determine whether the PE intervention reduces craving and alcohol consumption levels in BDs. The present project will involve: i) a pre-intervention comprehensive evaluation of behavioral (alcohol consumption), psychological (craving levels), physiological (VO2, HRV), and neurological (neuroimaging) variables; ii) a training phase consisting of 48 sessions (3 weekly sessions\*16 weeks) of aerobic (exp group 1), agility-cognitive (exp group 2) exercise and stretching (control group; iii) a post-intervention evaluation of behavioral, physiological, and neurological (neuroimaging) variables; iv) and a 6 months' follow- up evaluation of behavioral, physiologicaln and cognitive variables. A randomized controlled trial will be implemented at the University of Minho. It will include a total of 60 college students with a binge drinking pattern of alcohol intake, 20 participants per condition.

Interventions

BEHAVIORALAerobic Exercise

Participants allocated to the Aerobic condition will be following a 4 month-intervention aerobic exercise protocol of 3 weekly interleaved sessions with a 50 minutes duration

BEHAVIORALAgility-Cognitive Exercise

Participants allocated to the Agility-Cognitive condition will be following a 4 month-intervention agility-cognitive exercise protocol of 3 weekly interleaved sessions with a 50 minutes duration

BEHAVIORALStretching/relaxation

Participants allocated to the stretching control condition will be following a 4 month-intervention protocol of 1 weekly session with a 50 minutes duration

Sponsors

University of Minho
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

The protocol includes a randomized controlled trial with a follow-up at three months involving three groups of adolescents (18-24 Y) -experimental group 1, will be enrolled in the Aerobic program, experimental group 2 will be involved in the agility program, and an active control group that will be participating in a stretching program. Participants will be randomly assigned to each group.

Eligibility

Sex/Gender
ALL
Age
18 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

* binge drinking \> or = 5 ; \> or =4 for women alcoholic drinks * in the same time window (±2h) * at least once per month * \<150 minutes of physical activity per week

Exclusion criteria

* Major and/or unstable medical conditions * Physical limitations that may constraint the practice of exercise * Cardiovascular and respiratory insufficiency * History of traumatic brain injury or neurological disorder * Non-corrected sensory deficits * Personal history of psychopathological disorders * Family history of alcoholism or substance abuse in first degree relatives * Consumption of medical drugs with psychoactive effects (e.g., sedatives or anxiolytics) during the month previous to the assessment * Use of illegal drugs and AUDIT scores \>20 * MRI contraindications * Current or previous (past year) participation in a physical exercise program

Design outcomes

Primary

MeasureTime frameDescription
Brain function-resting stateThrough study completion, an average of 1 yearFunctional connectivity for resting-state fMRI
Brain structural connectivity- FAThrough study completion, an average of 1 yearStructural connectivity-fractional anisotropy-scalar value between zero and one within a voxel that describes the degree of anisotropy of a diffusion process
Brain structural connectivity - MDThrough study completion, an average of 1 yearStructural connectivity-mean diffusivity-a scalar measure between zero and one that describes the total diffusion within a voxel
Brain structural connectivity - ADThrough study completion, an average of 1 yearStructural connectivity-axial diffusivity-a scalar measure between zero and one within a voxel that describes the magnitude of diffusion parallel to fiber tracts.
Brain structural connectivity - RDThrough study completion, an average of 1 yearStructural connectivity-radial diffusivity-a scalar measure between zero and one within a voxel that describes the magnitude of diffusion parallel to fiber tracts.
Brain functionThrough study completion, an average of 1 yearBold signal for Task-related fMRI
Behavioral: alcohol consumptionThrough study completion, an average of 1 yearNumber of drinks per binge drinking episode
Behavioral: binge episodesThrough study completion, an average of 1 yearNumber of binge drinking episodes
Behavioral : drunkennessThrough study completion, an average of 1 yearPercentage of drunkenness
Psychological (craving levels)Through study completion, an average of 1 yearScores in the Alcohol Craving Questionnaire (The cutoff points for total scale points are: 12-17 = minimal desire, 18-25 = mild, 26-42 = moderate and 43 or more = severe)
Brain structureThrough study completion, an average of 1 yearStructure-volume in liters

Secondary

MeasureTime frameDescription
Monetary Incentive Delay Task (included in the fMRI paradigm) - reaction timeThrough study completion, an average of 1 yearReaction times, measured as seconds needed to give a response to assess the hypothetical differences in participant's level of achievement between the pretest, posttest and follow-up assessments.
Maximal oxygen consumption (VO2max)Through study completion, an average of 1 yearVO2max (ml/kg/min) will be measured in the pretest and posttest evaluations to assess the effects of the physical exercise protocol on cardiovascular fitness.
Brain-derived neurotrophic factor (BDNF)Through study completion, an average of 1 yearBDNF (pg/ml) concentrations measured in saliva will be measured in pre-intervention, post-intervention, at the midpoint of the intervention (2 months), and at the follow-up to assess the effects of the physical exercise protocol on neuroplasticity-related molecular markers.
DopamineThrough study completion, an average of 1 yearDopamine (pg/ml) concentrations measured in urine will be measured in pre-intervention, post-intervention, at the midpoint of the intervention (2 months), and at the follow-up to assess the effects of the physical exercise protocol on reward-related molecular markers.
Monetary Incentive Delay Task (included in the fMRI paradigm) - hitsThrough study completion, an average of 1 yearAccuracy, measured through the number of hits to assess the hypothetical differences in participant's level of achievement between the pretest, posttest and follow-up assessments.

Contacts

Primary ContactSónia Sousa, PhD
soniamachado@psi.uminho.pt+351917824280
Backup ContactAdriana Sampaio, PhD
adriana.sampaio@psi.uminho.pt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026