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Social RejectionPSDCP-2NCT07905430

Does Attachment Anxiety Moderate the Influence of Social Rejection on Alcohol Use Among Young Adults?

A study testing Social Rejection Feedback and Social Acceptance in people with Social Rejection and Attachement Style, run by University of North Carolina, Wilmington at 1 site in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Research shows that heavy drinking patterns are linked to many harmful consequences including death, sexual assault, risky sexual behavior, and drug use. Given such harmful consequences, it is important to identify the risk-factors for heavy "in-the-moment" drinking. Read more about this study

Who is it for?
Ages 21 to 25 yearsHealthy volunteers can take part
Conditions the study is for
Social Rejection, Attachement Style
What is being tested?
Social Rejection Feedback and Social Acceptance
Could I receive a placebo?
No, everyone receives an active treatment
How many people
152 participants
Where
1 siteUnited States
Study dates
5 Oct 2026to 23 Aug 2028
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 21 to 25 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Individuals must be 21-25 years of age;
  • Individuals are not pregnant;
  • Individuals have no history, or current diagnoses, of alcohol, drug, or psychiatric problems;
  • Individuals have no medical conditions, current or chronic, contraindicating alcohol use in the study;
  • Must be a regular drinker who is willing to taste a vodka-based beverage as part of the study.

Who cannot join

  • Individuals who are pregnant;
  • Individuals who have any medical or psychiatric problems that contraindicate the tasting of alcohol;
  • Individuals taking any medication or other substance that may interact negatively with the effects of alcohol;
  • Individuals who have substance abuse problems, or think they might have a substance abuse problem.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Richard S Pond, Ph.D. contact

910-962-3372

pondr@uncw.edu

United States1 site, 1 recruiting
  • University of North Carolina Wilmington

    Wilmington, North Carolina, 28403

    Recruiting

Other trials in United States

About this study

Official title: PERSONALITY, SOCIAL DYNAMICS, & CONSUMPTION PREFERENCES - STUDY 2

Research shows that heavy drinking patterns are linked to many harmful consequences including death, sexual assault, risky sexual behavior, and drug use. Given such harmful consequences, it is important to identify the risk-factors for heavy "in-the-moment" drinking. This study examines a potent, socially motivated trigger to problem drinking-namely, social rejection. In the present study, we employ a between-subjects experimental design with a sample of young adults (N=152; aged 21-25 years; 50% female) to examine how social rejection experiences are associated with drinking behavior as a function of attachment anxiety, changes in pain experience, and self-control.

Read the detailed description

Excessive alcohol use is a common but tragically destructive behavioral pattern, accounting for roughly 178,000 deaths per year in the United States in 2020 and 2021 (Centers for Disease Control and Prevention, 2024). This staggering estimate represents a 29% increase in the number of deaths due to drinking that was observed just a few years ago (between 2016 and 2017; Esser et al., 2024). Moreover, nearly a third of these alcohol-related deaths were due to "in-the-moment" binge drinking (Centers for Disease Control and Prevention, 2024). Clearly, more work is needed to identify the contextual and person-level risk factors that heighten one's vulnerability to drinking excessively and to develop effective interventions to ameliorate that risk. The present proposal focuses on one particular type of social risk factor-social rejection-that may be especially powerful in terms of increasing maladaptive drinking behavior, due to its capacity for enhancing pain experiences and diminishing self-regulatory restraint. Furthermore, in the present proposal, we identify a specific trait-attachment anxiety-that should serve as a significant, person-level risk factor, due to its association with threat appraisal, pain sensitivity, fear of rejection, and substance use. Thus, individual differences in attachment anxiety should amplify one's vulnerability to over-drinking after experiencing rejection. To date, we know that social rejection can cause people to drink greater amounts of alcohol compared to those who are socially accepted (Rabinovitz, 2014), particularly when that rejection comes from a close relationship partner (Laws et al., 2017). However, what remains unclear is why the link between social rejection and "in the moment" drinking exists and who among drinkers is most at risk. Our study was designed to fill this gap in the literature.

In the present study, we will recruit 152 carefully screened participants (aged 21 - 25) to participate in a double-blind between-subjects experiment to address the causal nature of the associations between social rejection and alcohol use. We will employ a two (social rejection vs. social acceptance) X two (male vs. female) double-blind between-subjects experimental design to examine the causal link between social rejection and drinking behavior and, further, whether increased pain experience and reduced self-control each mediate the effect of rejection on drinking. We do not expect significant gender differences in the pattern of mediation; however, we will include gender as a covariate factor, given inconsistent gender effects in the literature (see Bacon et al., 2015) and to maintain a balanced design. Finally, attachment anxiety will be examined as a potential, trait-level moderating factor.

Experimental Session:

  1. Informed Consent Process: The Experimental session will take place in a softly-lit, sound-controlled laboratory with three separate, private data collection rooms equipped with desks, chairs, and computers. Each room will be "treated" with vodka mist so that it smells like alcohol. Participants, aged 21 to 25 (established through checking driver's licenses), will enter the lab in groups of 3 (gender-matched). The session will begin with a research assistant (RA1; gender-matched) making introductions and starting the informed consent process. Participants will be told they will participate in a series of experiments in the UNCW Psychology Department and that "some of this research will require the tasting of alcoholic beverages," so participants must be willing and able to drink alcohol in a laboratory setting. During the informed consent process, participants will confirm that they know that they may stop the experimental procedure at any time, but, because they will consume alcohol, they must remain in the lab until their BAC level is zero. RA1 will then breath-test participants to confirm that their BAC is zero. Participants will then be asked if they complied with the substance use, food, and beverage intake requirements. Failure to comply, or a BAC above zero, will require rescheduling the appointment. Participants will then self-administer a pregnancy test (females only) and a urine drug test to confirm that they are not pregnant or currently using psychoactive drugs that might interfere with or mask alcohol effects. Participants will be told that the results of the tests will be confidential and only used to determine eligibility, after which the tests will be discarded. If an indicator is "positive", potential participants will be told that "the screening result indicates you may be ineligible today; we can discuss next steps privately".
  2. Screening: For participants that meet the qualifications, they will be asked to sign a consent form and provide their full name, date of birth, sex at birth, and city/municipality of birth for the generation of an anonymous, Global Unique Identifier compliant with NIAAA's requirements. This information will be collected and stored separately from all other participant data and will be destroyed at the end of the study. Participants will then be asked to complete a Screening Package containing the following instruments: Paper Questionnaires:
  3. Alcohol Use \& Drug Problems:
  • Alcohol Use Disorders Identification Test (AUDIT: Saunders et al., 1993)
  • Timeline Follow Back (TLFB: Sobell \& Sobell, 2000) / Daily Drinking Questionnaire (DDQ: Collins et al., 1985)
  • Drug Abuse Screening Test (DAST: Skinner, 19820
  • 90-day checklist of psychoactive substance use (Noel et al., 2015)
  1. Physical health:
  • CDC Adult Health History (CDC, 2011)
  1. Psychological health:
  • Brief Symptom Inventory (BSI: Derogatis \& Melisaratos, 1983) Electronic Questionnaires:
  1. Demographics (gender, marital status, race, ethnicity, education, height, \& weight)
  2. Trait moderators:
  • Attachment = Experiences in Close Relationships -Short Form (ECR-S: Wei et al., 2007)
  • Alcohol Expectancy Questionnaire - Revised (AEQ - Rohsenow, 1983)
  • Borderline Personality Symptoms = Personality Assessment Inventory - Borderline Scale (PAI-BOR: Morey, 1991)
  • Chronic Ostracism = Ostracism Experiences Scale (Carter-Sowell, 2010)
  • Childhood Trauma Questionnaire (CTQ: Bernstein \& Fink, 1998)
  1. Procedure:

After completing the initial consent and screening process for the experimental session, participants will be told that they are going to participate in a series of "decision-making" tasks (including the "get-to-know-you" paradigm, the Cued Go-No Go task, and taste-testing).

First, participants will take part in the "get-to-know-you paradigm" (a well-validated manipulation of rejection that reliably elicits strong feelings of social exclusion; Leary et al., 1995). Participants will be told that they will have the opportunity to get to know each other and then make a decision to work on the remaining study tasks individually or in a group. First, they will complete an essay about "what it means to be me?" and rate themselves on two bogus questionnaires with personality descriptors (e.g., "out-going", "shy"). However, they will be asked not to provide any identifying information within their essays. Participants will be informed that their essays and questionnaire responses will be distributed to each of the other two participants and that they will also read the materials from the other participants. After receiving and reading the distributed materials, participants will be asked to choose one individual with whom they would like to form a group for the next portion of the experiment. This will be done via the use of another questionnaire on which they will note the individual they would prefer to partner with for the next task based solely on their reading of the materials from the other participants.

Participants will then be randomly assigned to one of two conditions: social rejection or social acceptance.

For those assigned to the social acceptance condition, they will receive the following feedback:

"Unfortunately, as I was organizing the group materials, I noticed that we have run too many group conditions for the day. So even though everyone chose to work with you for the next portion, we won't be forming a group, and everyone will instead be working on their own."

Those assigned to the social rejection condition will receive the following feedback:

"Unfortunately, no one chose to work with you on the next task, so you will be engaging in the next task alone."

Following the rejection manipulation, participants will complete a manipulation check, a measure of state pain, and a measure of state affect (i.e., the Need Threat Scale, items from McGill Pain Questionnaire, \& PANAS) and then perform a version of the Cued Go-No Go task (Fillmore, 2003; our measure of self-regulation).

Next, alcohol consumption will be assessed through a taste-task procedure with a second, gender-matched "experimenter" (RA2; Noel et al., 2009). RA2, who is blind to the participant's experimental condition, will give the participant four chilled beverages in opaque plastic cups. Two will be labeled "alcoholic" and two will be labeled "no alcohol". We will give participants 150 ml total of the alcoholic beverage (divided equally into 75 ml per glass) and the same amount for the non-alcoholic beverage. The alcoholic beverage will be orange juice mixed with enough vodka to allow the participant to taste the alcohol. Based upon their height and weight, no participant will be given more alcohol than needed to reach a .03% BAC level of intoxication (i.e., our safety ceiling). We will use the Widmark Equation to determine amount of alcohol to distribute across participants [i.e., (Dose in grams/(Body weight in grams x Distribution ratio "r"))x100, where r(male)=.68 and r(female)=.55 and assuming an average constant rate of -0.016 BAC per hour.] The non-alcoholic beverage will be a lemonade mixture with no taste of vodka. Participants will have 20 minutes to rate each beverage according to a list of gustatory adjectives. RA 2 will then say that if the participant finishes his/her ratings during the 20 minutes, he or she is welcome to "finish any or all of the beverages you would like." RA 2 will then leave the room. After 20 minutes, RA 2 will return and collect the taste rating sheets and any remaining beverage. The Research Coordinator will measure the remainder of each participant's beverages (in ml) and subtract that from the original amount to calculate how much alcohol each participant consumed. All participants will then be fully debriefed and compensated for their participation.

After the debriefing, participants will be restricted from leaving until their BAC has reached zero, as measured by a breathalyzer. A snack will be provided and card games, videos, and so on will be available for entertainment.

Being tested
Social Rejection Feedback, Social Acceptance
Medical subject headings
Social Isolation

What participants receive

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

  • Social Rejection FeedbackBehavioural

    Those assigned to the social rejection condition will receive the following feedback:

    "Unfortunately, no one chose to work with you on the next task, so you will be engaging in the next task alone."

  • Social AcceptanceBehavioural

    For those assigned to the social acceptance condition, they will receive the following feedback:

    "Unfortunately, as I was organizing the group materials, I noticed that we have run too many group conditions for the day. So even though everyone chose to work with you for the next portion, we won't be forming a group, and everyone will instead be working on their own."

Study groups in NCT07905430
Study groupRoleWhat they receive
Social RejectionExperimentalNot described
Receives: Behavioral: Social Rejection Feedback
Social AcceptanceActive comparatorNot described
Receives: Behavioral: Social Acceptance

What is being measured

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

  1. Alcohol Consumption

    Participants will be given 150 ml total of the alcoholic beverage (orange juice mixed with enough vodka to allow the participant to taste the alcohol) and the same amount for the non-alcoholic beverage (lemonade mixture with no taste of vodka). Based upon their height and weight, no participant will be given more alcohol than needed to reach a .03% BAC level of intoxication (i.e., our safety ceiling). Participants will have 20 minutes to rate each beverage according to a list of gustatory adjectives. RA 2 will then say that if the participant finishes his/her ratings during the 20 minutes, he or she is welcome to "finish any or all of the beverages you would like." RA 2 will then leave the room. After 20 minutes, RA 2 will return and collect the taste rating sheets and any remaining beverage. The Research Coordinator will measure the remainder of each participant's beverages (in ml) and subtract that from the original amount to calculate how much alcohol each participant consumed.

    Measured: 20 minutes

Secondary outcomes (2)
  1. Inhibitory Control/Self-regulation

    Cued Go-No Go task (Fillmore, 2003)

    Measured: approximately 20 minutes

  2. State Pain Perceptions

    McGill Pain Questionnaire (Melzack, 1975)

    Measured: approximately 5 minutes

Timeline

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

  1. First posted29 Oct 2026
  2. Study start5 Oct 2026
  3. Primary completion23 Aug 2028 (estimated)
  4. Study completion23 Aug 2028 (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
Basic science
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Investigator, Outcomes assessor
Enrolment
152 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07905430
Sponsor's protocol ID
H26-0328
Other IDs
R15AA032936
Acronym
PSDCP-2
Status last verified
Oct 2026
First submitted
22 Oct 2026
Last updated
29 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The study has been pre-registered on the Open Science Framework (OSF). Materials used in the study will be uploaded to OSF. Data will be shared through OSF and the NIAAA Data Archive by request. Data will not include any identifiers or personal information.

Publications

  • Rabinovitz, S. (2014). Drowning your sorrows? Social exclusion and anger effects on alcohol drinking. Addiction Research & Theory, 22, 363-370.

  • Leary, M. R., Tambor, E. S., Terdal, S. K., & Downs, D. L. (1995). Self-esteem as an interpersonal monitor: The sociometer hypothesis. Journal of personality and social psychology, 68, 518-530.

  • Melzack R. The McGill Pain Questionnaire: major properties and scoring methods. Pain. 1975 Sep;1(3):277-299. doi: 10.1016/0304-3959(75)90044-5.

    PubMed 1235985
  • Noel NE, Maisto SA, Johnson JD, Jackson LA Jr. The effects of alcohol and cue salience on young men's acceptance of sexual aggression. Addict Behav. 2009 Apr;34(4):386-94. doi: 10.1016/j.addbeh.2008.11.016. Epub 2008 Nov 24.

    PubMed 19108956
  • Fillmore MT. Drug abuse as a problem of impaired control: current approaches and findings. Behav Cogn Neurosci Rev. 2003 Sep;2(3):179-97. doi: 10.1177/1534582303257007.

    PubMed 15006292
  • Esser MB, Sherk A, Liu Y, Naimi TS. Deaths from Excessive Alcohol Use - United States, 2016-2021. MMWR Morb Mortal Wkly Rep. 2024 Feb 29;73(8):154-161. doi: 10.15585/mmwr.mm7308a1.

    PubMed 38421934
  • Laws HB, Ellerbeck NE, Rodrigues AS, Simmons JA, Ansell EB. Social Rejection and Alcohol Use in Daily Life. Alcohol Clin Exp Res. 2017 Apr;41(4):820-827. doi: 10.1111/acer.13347. Epub 2017 Mar 2.

    PubMed 28253539
  • Bacon AK, Cranford AN, Blumenthal H. Effects of ostracism and sex on alcohol consumption in a clinical laboratory setting. Psychol Addict Behav. 2015 Sep;29(3):664-72. doi: 10.1037/adb0000054. Epub 2015 Feb 2.

    PubMed 25642585

Questions about this trial

What is this clinical trial studying?

A study testing Social Rejection Feedback and Social Acceptance in people with Social Rejection and Attachement Style, run by University of North Carolina, Wilmington 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 4 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: looking for participants now, 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?

Contact Richard S Pond, Ph.D. (910-962-3372, pondr@uncw.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Alcohol Consumption (time frame: 20 minutes). 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 NCT07905430, which also lists 8 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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