Skip to main content
OpenTrials
Completed

NCT Number: NCT01885312

Tailored Mobile Text Messaging to Reduce Problem Drinking

This study is designed to develop and test a tailored adaptive text messaging/short message service (SMS) intervention for individuals interested in stopping or reducing their alcohol consumption; and test and compare it to tailored but static, once a day messaging, gain framed messaging, and ecological momentary assessment only.

Completed

Looking for future studies?

Notify Me

Key information

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Feinstein Institute for Medical Research / North Shore-LIJ Health System

Great Neck, New York, 11021, United States

About this study

The proposed development study entitled, Tailored Mobile Text Messaging to Reduce Problem Drinking is designed to develop and test a tailored adaptive text messaging/short message service (SMS) intervention for individuals interested in stopping or reducing their alcohol consumption. This intervention includes messages tailored to baseline assessment results (including drinking times) that are adaptive to ongoing drinking patterns and goal achievement via interactive ecological momentary assessment (EMA). Other features include participant initiated help messaging and support network alerts. We will conduct beta research with 40 problem drinkers to assess messaging preferences and acceptability, and then conduct a pilot test with 10 PDs. In Stage 1b, we aim to test this intervention and understand the mechanisms of action of different text messaging interventions with 200 problem drinkers over a 12-week period. We propose to compare four types of messaging: 1) Tailored content and timed messaging adaptive to the participants current state (Stage 1a intervention); 2) Tailored content messaging (not adaptive or timed) sent at 3 pm every day; 3) Untailored consequence based messages sent at 3 pm every day; and 4) Brief feedback and EMA only. Assessments will be completed at baseline, through weekly EMA via SMS and at week 12 via a web-based follow-up assessment. Primary outcomes include drinks per drinking day, days of heavy drinking, and average drinks per week as measured through weekly EMA. Additional outcomes will include drinking related consequences, goal commitment and intervention satisfaction. Outcomes will be used to modify the intervention and to prepare for a larger Stage 1c RCT.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Participants must:

  • be fluent and able to read in English at the eighth grade level
  • be between the ages of 21 and 65
  • have an estimated average weekly consumption of greater than 15 or 24 standard drinks per week for women and men, respectively
  • be willing to reduce their drinking to non-hazardous levels
  • be willing to provide informed consent
  • own a mobile phone and have an active email address and are willing to receive and respond to up to 115 text messages total per month (average = 50)

Exclusion criteria

  • Participants will be excluded from the study if they
  • present with significant substance use or a current substance use disorder (for any substance other than alcohol, nicotine, or caffeine), which is defined as greater than once weekly use in the past month
  • present with a serious psychiatric illness or suicide risk as measured by previous inpatient treatment, medications for psychosis or recent suicidality; demonstrate clinically severe alcoholism, as evidenced by physical withdrawal symptoms or a history of serious withdrawal symptoms (e.g., hallucinations, seizures, or delirium tremens), and score greater than 12 on the Short Alcohol Withdrawal Scale (SAWS)
  • express a desire or intent to obtain additional substance abuse treatment while in the study
  • report a medical condition that precludes drinking any alcohol; or
  • demonstrate cognitive impairment as evidenced a score of less than 7 out of 10 on the consent form quiz

Treatment and study plan

Adaptive Tailored Intervention

Behavioral

Adaptive

Consequence-based Intervention

Behavioral

Loss Framed

Tailored, not adaptive, based Intervention

Behavioral

Baseline tailored not adaptive

Assessment only

Other

EMA only

Primary outcomes

  1. Days of Heavy Drinking (DHD)

    Time frame: 12 weeks

  2. Average Drinks per Week (ADW)

    Time frame: 12 weeks

Secondary outcomes

  1. Drinking Related Consequences

    Time frame: 12 weeks

  2. Goal Commitment

    Time frame: 12 weeks

Other outcomes

  1. Intervention Satisfaction

    Time frame: 12 weeks

Sponsors and collaborators

Lead sponsor

Northwell Health

Other

Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Registry information

Important dates

Study start
2014
Primary completion
2015
Study completion
2016
First posted
Jun 24, 2013
Registry last updated
Oct 13, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.