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Alcohol ConsumptionASPIRENCT06617702

Accountability Support Through Peer-Inspired Relationships and Engagement (ASPIRE) Trial

A study testing A text message alcohol intervention focused on cognitive, behavioral, and peer influences and A text message alcohol intervention focused on cognitive and behavioral influences in people with Alcohol Consumption, run by Stanford University at 1 site in United States.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

This project aims to test the efficacy of a text message intervention, ASPIRE, designed to address cognitive and behavioral elements and modify exposure to peers that influence drinking behaviors. Read more about this study

Who is it for?
Ages 18 to 25 years
Conditions the study is for
Alcohol Consumption
What is being tested?
A text message alcohol intervention focused on cognitive, behavioral, and peer influences and A text message alcohol intervention focused on cognitive and behavioral influences
Could I receive a placebo?
No, everyone receives an active treatment
How many people
300 participants
Where
1 siteUnited States
Study dates
10 Apr 2025to May 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 25 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Age 18-25 years (verified using date of birth)
  • Lives in the U.S. (based on zip code)
  • English reader (verified based on completing screen)
  • 2+ days with ≧4 standard alcohol drinks for women or ≧5 standard alcohol drinks for men in past month
  • Owns a mobile phone with SMS (verified by texting enrollment procedure)

Who cannot join

  • Currently enrolled or past enrollment in a 4-year college
  • Active military
  • Pregnant or pregnancy plans in the next 12-months
  • Prisoner status
  • Current or planned treatment for alcohol or substance use disorder in next 12-months

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Stanford University

    Palo Alto, California, 94306

Other trials in United States

About this study

Official title: ASPIRE to Change: Leveraging Text Messaging Peer Support Coaching to Mitigate Hazardous Alcohol Consumption in Non-Collegiate Young Adults

This project aims to test the efficacy of a text message intervention, ASPIRE, designed to address cognitive and behavioral elements and modify exposure to peers that influence drinking behaviors. Young adults who are contemplating reducing their drinking will be recruited from a national sample and randomized to ASPIRE versus a text message intervention focused solely on cognitive and behavioral elements. We will measure effectiveness at 3, 6, and 12 months, study mechanisms driving behavior change, and identify which subgroups stand to benefit most.

Being tested
A text message alcohol intervention focused on cognitive, behavioral, and peer influences, A text message alcohol intervention focused on cognitive and behavioral influences
Keywords
alcohol, text message, young adults, peers
Medical subject headings
Alcohol Drinking

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • A text message alcohol intervention focused on cognitive, behavioral, and peer influencesBehavioural

    Each Thursday and Sunday ASPIRE will conduct brief text message communication aimed at modifying cognitive (e.g.desire to get drunk), behavioral (e.g.alcohol consumption), and peer influences (e.g.peer pressure and support).

  • A text message alcohol intervention focused on cognitive and behavioral influencesBehavioural

    Each Thursday and Sunday ASPIRE will conduct brief text message communication aimed at modifying cognitive (e.g. desire to get drunk) and behavioral (e.g. alcohol consumption) influences.

Study groups in NCT06617702
Study groupRoleWhat they receive
A text message alcohol intervention focused on cognitive, behavioral, and peer influencesExperimentalNot described
Receives: Behavioral: A text message alcohol intervention focused on cognitive, behavioral, and peer influences
A text message alcohol intervention focused on cognitive and behavioral influencesActive comparatorNot described
Receives: Behavioral: A text message alcohol intervention focused on cognitive and behavioral influences

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Binge Drinking Days (BDD)

    We define BDD as a day when a woman reports 4 or more standard drinks or a man reports 5 or more standard drinks, as this equates to the alcohol consumption that raises blood alcohol concentration to 0.08 g/dl or above.

    Measured: 3, 6, and 12 months

Secondary outcomes (1)
  1. Negative Alcohol Consequences (NAC) Scale Score

    We calculate the number of NAC using the Brief Young Adult Alcohol Consequences Questionnaire (B-YAACQ). The B-YAACQ is a 24-item measure of alcohol-related problems that utilizes a dichotomous (present or absent) scoring format. Higher scores indicate both wider variety and more severe pattern of alcohol-related problems.

    Measured: 3, 6 and 12 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Sep 2024
  2. Study start10 Apr 2025
  3. Primary completionDec 2026 (estimated)
  4. Study completionMay 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
300 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06617702
Sponsor's protocol ID
76956
Other IDs
1R01AA030986-01A1
Acronym
ASPIRE
Status last verified
Oct 2026
First submitted
26 Sep 2024
Last updated
29 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: All test message and web-based data from baseline through 12-month followups will be uploaded to the data repository (the National Institute on Alcohol Abuse and Alcoholism Data Archive (NIAAADA).

Publications

  • Kahler CW, Hustad J, Barnett NP, Strong DR, Borsari B. Validation of the 30-day version of the Brief Young Adult Alcohol Consequences Questionnaire for use in longitudinal studies. J Stud Alcohol Drugs. 2008 Jul;69(4):611-5. doi: 10.15288/jsad.2008.69.611.

    PubMed 18612578
  • Sobell LC, Brown J, Leo GI, Sobell MB. The reliability of the Alcohol Timeline Followback when administered by telephone and by computer. Drug Alcohol Depend. 1996 Sep;42(1):49-54. doi: 10.1016/0376-8716(96)01263-x.

    PubMed 8889403
  • Rueger SY, Trela CJ, Palmeri M, King AC. Self-administered web-based timeline followback procedure for drinking and smoking behaviors in young adults. J Stud Alcohol Drugs. 2012 Sep;73(5):829-33. doi: 10.15288/jsad.2012.73.829.

    PubMed 22846247

Questions about this trial

What is this clinical trial studying?

A study testing A text message alcohol intervention focused on cognitive, behavioral, and peer influences and A text message alcohol intervention focused on cognitive and behavioral influences in people with Alcohol Consumption, run by Stanford University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 29 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Binge Drinking Days (BDD) (time frame: 3, 6, and 12 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06617702, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Oct 2026.

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