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Not yet recruitingNCT06670794Updated Jul 2, 2026

Using Ecological Momentary Data to Inform a Web Intervention for Romantic Partners Concerned About Their Loved Ones' Drinking

An interventional study of Web-based intervention for concerned partners and Psychoeducation control in Experimental and Control Condition, sponsored by University of Florida. Not yet recruiting. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-02.

Sponsored by University of Florida · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
160
Allocation
Randomized
Ages
18 Years and older
Sex
All
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Study summary

Aim 1. Couples (N=50 dyads) with a Concerned Partner (CP) and a Drinking Partner (DP) will independently complete baseline and follow-up surveys and a 21-day EMA with three daily reports on their communication and DP's drinking. Aim 2. Iteratively develop a four-session web based intervention and evaluate the WBI's feasibility and acceptability with 15 CPs. Aim 3. Perform a pilot randomized controlled trial (RCT) comparing WBI to psychoeducation control in 110 couples.

Read the detailed description

Alcohol misuse negatively affects relationships and is significantly correlated with higher rates of relationship conflict, distress, and dissolution as well as other serious negative interpersonal consequences (e.g., domestic violence, sexual assaults). Encouragement from concerned partners (CPs) is a common motivator for those who misuse alcohol to pursue care and often the most helpful mechanism in supporting change. The goals of this proposal are to: Identify how specific CP behaviors influence their partner's alcohol craving, motives, drinking, and problems on a daily basis using dyadic ecological momentary assessment techniques (Aim 1); use the knowledge from EMA analysis to iteratively develop a CP-focused web-based intervention (WBI) that provides psychoeducation about communication patterns that influence DP drinking and by integrating personalized feedback about CPs' own communication behaviors that may be working against their goals (Aim 2); and pilot the WBI's efficacy on CP outcomes (depression, anxiety, social support), their partner's drinking behavior (alcohol consumption, motives, related consequences), and both partners' relationship distress and conflict (Aim 3). The investigators expect the WBI will yield significant improvements in all outcomes. This project is significant because intervening with CPs has strong potential to change relationship dynamics that may reduce problems and prevent future problems associated with alcohol misuse. It also develops a new prevention model that does not rely on the drinking partner attending a clinical facility to access care. The proposed study is innovative because it uses dyadic and ecological momentary assessment designs to test dynamic questions about interdependence in relationship interactions and alcohol use between partners and employs the generated knowledge to inform intervention adaptation. Teaching CPs to effectively communicate their concerns may be a necessary catalyst for decreasing their partner's alcohol use and preventing alcohol use disorders. The potential reach of this intervention is large such that it can be easily implemented over the web to those who may need help but would not otherwise seek care.

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Conditions studied

  • Experimental
  • Control Condition

Keywords

  • alcohol
  • alcohol use disorder
  • community reinforcement and family training
  • concerned partners
  • concerned significant others
  • communication
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In context

Alcoholism

1,674 studies on the registry are indexed under Alcoholism; 331 are open to participants now.

This study's planned enrollment of 160 is above the median of 88 across 1,428 interventional studies indexed under Alcoholism.

Browse Alcoholism studies →

Lead sponsor

University of Florida is the lead sponsor of 1,287 studies on the registry; 199 are open to participants now.

Of its 180 completed or terminated interventional studies of FDA-regulated products, 143 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

CP Inclusion Criteria:

  • be at least 18 years old
  • be in a romantic relationship with their partner
  • be living with their partner,
  • have a computer, tablet, or mobile phone with Internet access
  • have no plans to separate from their partner in the next 60 days
  • indicate no concerns they would be physically hurt by their partner on the Intimate Partner Screen

CP Exclusion Criteria:

  • drinking scores at or above the threshold for DP participation

DP Inclusion Criteria:

  • be at least 18 years old
  • misuses alcohol as defined by their scores (4+ for women/non-gender confirming, 5+ for men) on the consumption portion of the Alcohol Use Disorder Identification Test (AUDIT-C) (Dawson et al., 2005)
  • has a computer, tablet, or mobile phone with Internet access
  • indicates no concerns they would be physically hurt by their partner

DP Exclusion Criteria:

  • current alcohol treatment
  • currently concerned about their partner's drinking
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
160 participants (estimated)

Study arms

  • Other
    Psychoeducation control

    Psychoeducation control CPs will be routed to visit self-help resources on NIAAA's website ("Alcohol's Effects on Health") and asked to spend the same amount of time (20-30 minutes) reviewing site content.

    Behavioral: Psychoeducation control

  • Experimental
    Experimental web-based intervention

    CPs in the experimental web-based intervention condition will complete web-based sessions including personalized feedback and information about how communication and self-care affect their own well-being and their partner's alcohol use behaviors.

    Behavioral: Web-based intervention for concerned partners

Interventions

  • BehavioralWeb-based intervention for concerned partners

    The web-based intervention will comprise sessions focusing on community reinforcement and family therapy principles including: (1) self-care, (2) positive communication including ways to increase responsiveness to their partner (PPR; i.e., actively listening, showing understanding, expressing interest in what their partner is thinking and feeling, and trying to see where their partner is coming from), (3) understanding their partner's drinking reinforcers, and (4) supporting their partner if they want help and engaging in positive, healthy activities with their partner.

  • BehavioralPsychoeducation control

    This is a psychoeducation control condition.

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What researchers measure

Primary outcomes

  1. CP Depression Symptoms Questionnaire

    Patient Health Questionnaire. 8 items. Scores range from 0-32. Higher scores indicate more depressive symptoms.

    Time frame: 1 month post-intervention.

  2. CP Anxiety Symptoms Questionnaire

    Generalized Anxiety Disorder scale. 7 items. Higher scores indicate more anxiety symptoms.

    Time frame: 1 month post-intervention.

  3. CP Anger expression questionnaire

    Dimensions of Anger Reactions - 5 item (DAR-5). Scores range 1-5 with higher scores indicating greater anger.

    Time frame: 1 month post-intervention.

  4. CP Loneliness Questionnaire

    Measure: UCLA 3-item Loneliness Scale (Hughes, M. E., Waite, L. J., Hawkley, L. C., \& Cacioppo, J. T. (2004). A Short Scale for Measuring Loneliness in Large Surveys. Research on Aging, 26(6), 655-672. https://doi.org/10.1177/0164027504268574) Scores are 1-9. Higher scores indicate more loneliness.

    Time frame: 1 month post-intervention.

  5. CP Partner Social Support Questionnaire

    Marital Perceived Social Support (Cohen et al., 1985). Scored 0-3. Higher scores mean more social support.

    Time frame: 1 month post-intervention.

  6. CP-DP Relationship Functioning Questionnaire

    Quality of Marriage Index (Norton, 1983). Higher scores indicate greater relationship satisfaction.

    Time frame: 1 month post-intervention.

  7. DP AUDIT Questionnaire

    Drinking Partner's AUDIT score. 10 items. Items are summed. Greater scores indicate greater alcohol use.

    Time frame: 1 month post-intervention.

  8. CP General Social Support Questionnaire

    MOS Social Support Survey (Sherbourne \& Stewart, 1991). Scored 1-5. Higher scores indicate more social support. Sherbourne, C. D., \& Stewart, A. L. (1991). The MOS social support survey. Social science \& medicine, 32(6), 705-714.

    Time frame: 1 month post-intervention.

  9. DP Alcohol Use Questionnaire

    Drinking Partner's: Alcohol consumption via the Quantity/Frequency/Peak Alcohol Use Index (Dimeff et al., 1991). Six items measure the drinking partner's alcohol consumption. The items are not scored together but evaluated individually (e.g., frequency, typical quantity, peak quantity, etc.). Higher scores denote greater consumption.

    Time frame: 1 month post-intervention.

  10. DP Drinking Motives Questionnaire

    Drinking Partner's Drinking Motives using the Drinking Motives Questionnaire (Cooper et al., 1992). Subscales for coping, enhancement, social, and conformity. Items are averaged. Higher scores indicate greater endorsement of that motive.

    Time frame: 1 month post-intervention.

  11. DP Alcohol-related Consequences Questionnaire

    Drinking Partner's Alcohol-related Consequences assess via the Brief Young Adult Alcohol Related Consequences measure. 24 items. Scores are created by summing the items. Higher scores denote greater consequences endorsed.

    Time frame: 1 month post-intervention.

Secondary outcomes

  1. CP-DP Communication Questionnaire

    Family Environment via the Brief Family Relationship Scale. Fok, C. C., Allen, J., Henry, D., \& People Awakening Team (2014). The brief family relationship scale: a brief measure of the relationship dimension in family functioning. Assessment, 21(1), 67-72. https://doi.org/10.1177/1073191111425856. Cohesion, expressiveness, and conflict subscales. Items are averaged. For each subscale, greater scores reflect greater cohesion, expressiveness, and constructive ways of handling conflict.

    Time frame: 1 month post-intervention.

  2. CP-DP Perceived Partner Responsiveness Questionnaire

    Measures perceived partner responsiveness. Scores range from 1-5. Greater scores mean greater responsiveness perceived about the partner. Source articles: Laurenceau, J. P., Barrett, L. F., \& Pietromonaco, P. R. (1998). Intimacy as an interpersonal process: The importance of self-disclosure, partner disclosure, and perceived partner responsiveness in interpersonal exchanges. Journal of Personality and Social Psychology, 74(5), 1238-1251. https://doi.org/10.1037//0022-3514.74.5.1238 O'Neill, A.S., Mohr, C.D., Bodner, T., \& Hammer, L. (2020). Perceived Partner Responsiveness, Sleep and Pain: A Dyadic Study of Military-Connected Couples. Health Psychology, 39(12), 1089-1099. https://doi.org/10.1037/hea0001035

    Time frame: 1 month post-intervention.

  3. CP Communication about Drinking Questionnaire

    We have created a measure adapted from the Spouse Behavior Questionnaire (Love et al., 1991) and the Partner Management Strategies Questionnaire (Rodriguez et al., 2013) that will assess different behaviors CPs use to attempt to change their partner's drinking. Subscales include punishing drinking, rewarding sobriety, withdrawing, and supporting drinking. Items are averaged. Higher scores mean greater endorsement of these subscales.

    Time frame: 1 month post-intervention.

  4. CP-DP Communication: Number of conflicts

    We will ask participants the number of disagreements they have had with their partner. Higher numbers denote more disagreements.

    Time frame: 1 month post-intervention.

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: Yes — The data will be deidentified, but shared data will be at the individual level.

Supporting information: Study protocol, Statistical analysis plan, Analytic code

Time frame: Data will be available within 2 years of the award end date, as required by the NIAAA Data Archive. Data will also be grouped based on publication, which will be shared when the pre-print is available. These publications will have DOIs to aid in findability. Raw data will include a GUID to help with indexing. The NIAAA Data Archive will make decisions about how long to preserve data.

Access criteria: Any scientific researcher may access our de-identified data, as consistent with the NIAAA Data Archive. To request access of the data, researchers will use the standard processes for the NIAAA Data Archive, and the Data Access Committee will decide which requests to grant. The standard NIAAA data access process allows access for one year and is renewable. Data will be findable for the research community through utilization of the NIAAA Data Archive, which is a public data repository housed under the NIMH. All participants will be assigned a GUID to allow for standard indexing. Research publications and manuscripts will be assigned a digital object identifier (DOI), which will be referenced in the data, to allow for the research community to access the exact information used for this publication.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06670794
Responsible party
Sponsor
First posted
Nov 1, 2024
Start date
Sep 29, 2026 (estimated)
Primary completion
Feb 28, 2027 (estimated)
Completion
Feb 28, 2027 (estimated)
Last update
Jul 2, 2026

Study contacts

Lindsey Rodriguez, Ph.D.
Contact
lmrodriguez@ufl.edu
650-613-3484
Karen Osilla, Ph.D.
Contact
kosilla@stanford.edu
Lindsey Rodriguez, Ph.D.
principal investigator · University of Florida

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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