Heavy Drinking

7

Review clinical trials related to Heavy Drinking. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Reset Challenge: Reducing High-risk Drinking for Cancer Prevention

This is a single-arm, non-randomized, prospective study to evaluate the feasibility and preliminary efficacy of a 30-day mobile Health (mHealth) Reset Challenge for reducing high-risk drinking.

Participants needed: 150
Trial details
Age: 18-120Biological sex: AllType: InterventionalSponsor: University of OklahomaUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Adults +18 [+3]

Status: Recruiting

Affirmative Psychotherapy for Sexual Minority Women's Mental and Behavioral Health

The purpose of this 2-arm randomized controlled trial is to assess the efficacy of a 10-session lesbian, gay, bisexual, transgender, and queer (LGBTQ)-affirmative cognitive-behavioral psychotherapy (CBT) delivered via telehealth in a large sample of sexual minority women (SMW) in New York, New Jersey and Pennsylvania. The investigators will assess whether the EQuIP (Empowering Queer Identities in Psychotherapy) treatment demonstrates significant reductions in heavy drinking (HD) and mental health symptoms (e.g., depression) compared to LGBTQ-affirmative treatment-as-usual.

Participants needed: 274
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Yale UniversityUpdated: Jun 15, 2026Locations: 1
Eligibility criteria

be 18 years of age or older [+2]

report current mental health treatment ≥1 day/mo [+7]

Status: Recruiting

Exploring the Effects of Brief Mindfulness Training With Vagal Nerve Stimulation on Alcohol Cue Reactivity Among Young Adult Heavy Drinkers

The present study will assess the acceptability and feasibility of a brief intervention designed to help young heavy drinkers reduce their alcohol consumption. All participants will complete a brief (1-week) mindfulness intervention, and participants will be randomized to receive either active or inactive Respiratory-gated Auricular Vagal Afferent Nerve Stimulation (RAVANS) during two in-person laboratory visits. Heart rate variability data and self-report survey data will be collected to assess the impact of the intervention on autonomic regulation, alcohol consumption, and additional clinical measures.

Participants needed: 50
Trial details
Age: 21-29Biological sex: AllType: InterventionalSponsor: Cambridge Health AllianceUpdated: May 12, 2026Locations: 1
Eligibility criteria

Currently living in Massachusetts. [+5]

Current or past diagnosis of a substance use disorder based on the Quick Structu... [+17]

Status: Recruiting

Alcohol-ROC-Training

The goal of the proposed study is to examine whether brief training in regulation of craving (ROC-T) affects alcohol drinking. The study will consist of a basic screening (phone and online), and in person visit to determine eligibility and conduct pre-intervention baseline assessments, 1-4 training (ROC-T) visits, a post-intervention assessment visit, and 1-2 phone/online follow up assessments.The two active conditions of ROC-T are based on cognitive-behavioral treatments (CBT) and mindfulness-based treatments (MBT).

Participants needed: 177
Trial details
Age: 18-26Biological sex: AllType: InterventionalSponsor: Yale UniversityUpdated: Feb 19, 2026Locations: 2
Eligibility criteria

Not listed

Status: Recruiting

Aerobic Exercise Addition to Cognitive Behavioural Treatment in Impotence Metabolic-syndrome Drinkers

Cognitive Behavioural Treatment is used as treatment for Heavy Drinking, Impotence, and Metabolic Syndrome. The efficacy of adding aerobic training to this treatment is not tested till now.

Participants needed: 40
Trial details
Age: 35-45Biological sex: MaleType: InterventionalSponsor: Cairo UniversityUpdated: Dec 11, 2025Locations: 1
Eligibility criteria

heavy drinking men (forty) [+2]

cardiac problems [+1]

Status: Not yet recruiting

Helpline Pilot Factorial Trial

The pilot factorial trial will (1) evaluate feasibility, acceptability, and fidelity of the intervention components (Aim 2.1), and (2) collect proof-of-concept data on the impact of the components on the proximal (motivation, self-efficacy, and self-regulation) and distal (quantity and frequency of HED) outcomes (Aim 2.2). Participants will include 120 postpartum mothers recruited from social media. The investigators will conduct a pilot 2X2X2 balanced full factorial trial, with 4 factors (1 constant, 3 randomized to 2 levels each) and 8 study conditions. The 4 factors will include: (1) Standard Helpline (constant); (2) Motivational Interviewing (yes vs. no); (3) Coping skills training (yes vs. no); (4) Automated messaging (yes vs. no). Participants will be randomly assigned to one of 8 study conditions, which will determine which combination of intervention components participants receive.

Participants needed: 120
Trial details
Phase: Phase 1Age: 18-45Biological sex: FemaleType: InterventionalSponsor: The National Center on Addiction and Substance Abuse at Columbia UniversityUpdated: Jan 15, 2025
Eligibility criteria

Resides full-time in the United States [+6]

Resides outside of the United States [+7]

Status: Not yet recruiting

Study of Nitrate-Rich Juice on Cognitive Function in Heavy Alcohol Drinkers: a Two-Stage Adaptive Design Real-World Clinical Trial

It is known that alcohol consumption can lead to cognitive impairment and dysregulation of inflammatory responses. A preliminary randomized controlled trial conducted by our research team has suggested that nitrate may improve cognition in hospitalized patients with alcohol dependence. To further expand the population and applicability, this study aims to explore the effects of nitrate on cognition in a real-world population of heavy drinkers. The researchers have designed a two-stage clinical trial: the first stage involves the analysis of existing data, and the second stage will recruit 43-54 new participants for a 14-day dietary inorganic nitrate (nitrate-rich beetroot juice, \~750 mg NO3- /d) intervention.

Participants needed: 43
Trial details
Biological sex: AllType: InterventionalSponsor: Peking University Sixth HospitalUpdated: Jan 15, 2025
Eligibility criteria

Not listed