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Using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial
BACKGROUND: Alcohol abuse, other substance use disorders, and risk behaviors associated with the human immunodeficiency virus (HIV) represent three of the top 10 modifiable causes of mortality in the US. Despite evidence that continuing care is effective in sustaining recovery from substance use dis...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5553728/ https://www.ncbi.nlm.nih.gov/pubmed/28797307 http://dx.doi.org/10.1186/s13063-017-2096-z |
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author | Scott, Christy K Dennis, Michael L. Gustafson, David H. |
author_facet | Scott, Christy K Dennis, Michael L. Gustafson, David H. |
author_sort | Scott, Christy K |
collection | PubMed |
description | BACKGROUND: Alcohol abuse, other substance use disorders, and risk behaviors associated with the human immunodeficiency virus (HIV) represent three of the top 10 modifiable causes of mortality in the US. Despite evidence that continuing care is effective in sustaining recovery from substance use disorders and associated behaviors, patients rarely receive it. Smartphone applications (apps) have been effective in delivering continuing care to patients almost anywhere and anytime. This study tests the effectiveness of two components of such apps: ongoing self-monitoring through Ecological Momentary Assessments (EMAs) and immediate recovery support through Ecological Momentary Interventions (EMIs). METHODS/DESIGN: The target population, adults enrolled in substance use disorder treatment (n = 400), are being recruited from treatment centers in Chicago and randomly assigned to one of four conditions upon discharge in a 2 × 2 factorial design. Participants receive (1) EMAs only, (2) EMIs only, (3) combined EMAs + EMIs, or (4) a control condition without EMA or EMI for 6 months. People in the experimental conditions receive smartphones with the apps (EMA and/or EMI) specific to their condition. Phones alert participants in the EMA and EMA + EMI conditions at five random times per day and present participants with questions about people, places, activities, and feelings that they experienced in the past 30 min and whether these factors make them want to use substances, support their recovery, or have no impact. Those in the EMI and EMA + EMI conditions have continual access to a suite of support services. In the EMA + EMI condition, participants are prompted to use the EMI(s) when responses to the EMA(s) indicate risk. All groups have access to recovery support as usual. The primary outcome is days of abstinence from alcohol and other drugs. Secondary outcomes are number of HIV risk behaviors and whether abstinence mediates the effects of EMA, EMI, or EMA + EMI on HIV risk behaviors. DISCUSSION: This project will enable the field to learn more about the effects of EMAs and EMIs on substance use disorders and HIV risk behaviors, an understanding that could potentially make treatment and recovery more effective and more widely accessible. TRIAL REGISTRATION: ClinicalTrials.gov, ID: NCT02132481. Registered on 5 May 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-2096-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5553728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55537282017-08-15 Using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial Scott, Christy K Dennis, Michael L. Gustafson, David H. Trials Study Protocol BACKGROUND: Alcohol abuse, other substance use disorders, and risk behaviors associated with the human immunodeficiency virus (HIV) represent three of the top 10 modifiable causes of mortality in the US. Despite evidence that continuing care is effective in sustaining recovery from substance use disorders and associated behaviors, patients rarely receive it. Smartphone applications (apps) have been effective in delivering continuing care to patients almost anywhere and anytime. This study tests the effectiveness of two components of such apps: ongoing self-monitoring through Ecological Momentary Assessments (EMAs) and immediate recovery support through Ecological Momentary Interventions (EMIs). METHODS/DESIGN: The target population, adults enrolled in substance use disorder treatment (n = 400), are being recruited from treatment centers in Chicago and randomly assigned to one of four conditions upon discharge in a 2 × 2 factorial design. Participants receive (1) EMAs only, (2) EMIs only, (3) combined EMAs + EMIs, or (4) a control condition without EMA or EMI for 6 months. People in the experimental conditions receive smartphones with the apps (EMA and/or EMI) specific to their condition. Phones alert participants in the EMA and EMA + EMI conditions at five random times per day and present participants with questions about people, places, activities, and feelings that they experienced in the past 30 min and whether these factors make them want to use substances, support their recovery, or have no impact. Those in the EMI and EMA + EMI conditions have continual access to a suite of support services. In the EMA + EMI condition, participants are prompted to use the EMI(s) when responses to the EMA(s) indicate risk. All groups have access to recovery support as usual. The primary outcome is days of abstinence from alcohol and other drugs. Secondary outcomes are number of HIV risk behaviors and whether abstinence mediates the effects of EMA, EMI, or EMA + EMI on HIV risk behaviors. DISCUSSION: This project will enable the field to learn more about the effects of EMAs and EMIs on substance use disorders and HIV risk behaviors, an understanding that could potentially make treatment and recovery more effective and more widely accessible. TRIAL REGISTRATION: ClinicalTrials.gov, ID: NCT02132481. Registered on 5 May 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-017-2096-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-10 /pmc/articles/PMC5553728/ /pubmed/28797307 http://dx.doi.org/10.1186/s13063-017-2096-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Study Protocol Scott, Christy K Dennis, Michael L. Gustafson, David H. Using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial |
title | Using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial |
title_full | Using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial |
title_fullStr | Using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial |
title_full_unstemmed | Using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial |
title_short | Using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial |
title_sort | using smartphones to decrease substance use via self-monitoring and recovery support: study protocol for a randomized control trial |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5553728/ https://www.ncbi.nlm.nih.gov/pubmed/28797307 http://dx.doi.org/10.1186/s13063-017-2096-z |
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