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Integrated Digital Health Approach to Reduce Hazardous Alcohol Use and Chronic Pain Among Rural Populations

Alcohol Use and Pain in Rural Populations

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07804914
Enrollment
260
Registered
2026-09-04
Start date
2027-02-01
Completion date
2030-12-01
Last updated
2026-09-04

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

Conditions

Chronic Pain, Unhealthy Alcohol Use

Keywords

chronic pain, unhealthy alcohol use, hazardous/harmful drinking, digital health

Brief summary

The current proposal seeks to test the benefit of a brief intervention combined with a digital program delivered though a smartphone app for reducing chronic pain and hazardous drinking among those in rural settings. Participants are recruited through social media and complete an online pre-screener and telephone screener to determine eligibility. All subsequent study assessment procedures are conducted through videoconferencing online. Participants complete 3 assessments over the course of 8 months. Following the first (baseline assessment) participants are randomized to either the INTERVENTION (INTV) or a treatment-as-usual CONTROL (CTL) condition. Those in the INTV condition meet with a health counselor for up to 50 minutes and then complete an 8-week smartphone-based intervention with weekly SMS based brief coaching. This in the CTL group meet with the health counselor only. Participants complete additional assessments at 3-months and 8-months post -baseline. Measures of alcohol use and pain are assessed after the intervention at 3 months and at the final outcome period at 8-months post-baseline.

Detailed description

The current proposal represents an extension of previous research on the use of a smartphone-based intervention to reduce chronic pain and hazardous drinking among those in rural settings. The study is a randomized controlled trial that tests the efficacy of digital intervention for reducing pain intensity and interference and the quantity of alcohol consumption. Participants are recruited through social media and complete an online pre-screener to determine eligibility. This is followed by a telephone screener to confirm eligibility before scheduling baseline. All subsequent study assessment procedures are conducted through videoconferencing online. Following baseline assessment guided by an RA, participants are randomized to the INTERVENTION (INTV) or a treatment-as-usual CONTROL (CTL). Those in the INTV condition meet with a health counselor for up to 50 minutes and then complete an 8-week smartphone-based intervention with weekly SMS based brief coaching. This in the CTL group meet with the health counselor only. Participants complete additional assessments at 3-months and 8-months post -baseline. The 8-month assessment is the primary timepoint and assesses pain experience and alcohol use as measured by self-report and phosphatidylethanol (PEth) from a participant administered, RA supervised, finger stick. It is hypothesized that those in the INTV condition will show lower ratings of pain and less alcohol consumption at 8-months post-baseline.

Interventions

BEHAVIORALMobile Intervention for Alcohol and Pain

The Intervention (INTV) is a brief motivational intervention with a health counselor followed by an 8-week smartphone-based program in which participants are provided with cognitive behavioral and self-management skills to reduce hazardous drinking and chronic pain. They practice skills using the app and have weekly contact with the health counselor through instant messaging

BEHAVIORALControl Intervention

Participants are provided with psychoeducation about the reciprocal influences of hazardous drinking and chronic pain and their joint effects on health outcomes. In addition, they are provided with information about free web-based national resources should they wish to receive more information or additional help with pain or drinking

Sponsors

Boston University Charles River Campus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Outcome assessment will be conducted by a research assistant who is blind to the randomization condition

Intervention model description

Two condition, between-groups design, randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Reside in a US rural area (non-metropolitan country) as defined by the Rural-Urban Commuting Codes from US Dept. of Agriculture * At least 18 years of age * Engage in hazardous drinking (either by exceeding weekly NIAAA guidelines of 7 standard drinks for women \[\>7\] and those \> 65 and older or 14 for men \[\>14\] \<65, and/or having at least one heavy drinking episode in the past month as measured by \>3 drinks for women and those \> 65 and \>4 drinks for men \< 65), - - Experience chronic pain (at least 3 months in duration) of at least moderate severity (4 or greater on the Numerical Pain Rating Scale) * Fluent in English * Use of a personal smartphone * Able to provide the name and contact information for one or more individuals who may be contacted in case the participant cannot be reached at follow-up.

Exclusion criteria

* History of bipolar disorder, schizophrenia, or other psychotic disorders * Prior history of serious alcohol-related withdrawal symptoms (i.e., withdrawal-related seizures or delirium tremens) * Current psychological/behavioral treatment for alcohol use disorder * Current psychological/behavioral treatment for chronic pain * Cancer-related pain * Intent to have surgery for a pain-related condition in the next 8-months * If using psychoactive medications for pain management or alcohol use must be using a stable medication dose (same dose for at least 2 months).

Design outcomes

Primary

MeasureTime frameDescription
Pain, Enjoyment of Life, and General Activity Scale (PEG)rating in the past week taken at (1) Baseline (2) 12-weeks post baseline, (3) 32-weeks post baseline. Note that 12-week and 32-week measures have up to 1 month window [i.e., 1 month post scheduled date for assessment] for completion3-item, 0-10 numerical scale measure of pain
Average number of alcohol-containing drinks consumed per week: Time-Line Followback-30past 30 day drinking report taken at (1) Baseline (2) 12-weeks post baseline, (3) 32-weeks post baseline. Note that 12-week and 32-week measures have up to 1 month window [i.e., 1 month post scheduled date for assessment] for completionCalendar-based measure of alcohol consumption in the past 30 days
Number of heavy drinking days in past month: Time-Line Followback-30 [TLFB-30]number of days in the past 30. drinking report taken at (1) Baseline (2) 12-weeks post baseline, (3) 32-weeks post baseline.. Note that 12-week and 32-week measures have up to 1 month window [i.e., 1 month post scheduled date for assessment] for compleFrom the TLFB-30, the number of days in the past month in which a participant engaged in heavy drinking \[defined as 4+ for women and 5+ for men\], 4 or more for those 65 and over.

Secondary

MeasureTime frameDescription
Short Inventory of Problems - Revisedconsequences in past 90 days....measure taken at baseline, 12-weeks post-baseline, and 32-weeks post-baseline. Note that 12-week and 32-week measures have up to 1 month window [i.e., 1 month post scheduled date for assessment] for completionSeventeen, 4-category Likert scale item (from never to daily/almost daily) that assesses 17 common alcohol-related consequences

Countries

United States

Contacts

CONTACTTibor P Palfai, PhD
palfai@bu.edu617-353-9345
CONTACTSarah Fraher, BA
sfraher@bu.edu
PRINCIPAL_INVESTIGATORTibor P Palfai, PhD

Boston University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 5, 2026