Skip to main content
OpenTrials
Completed

NCT Number: NCT03301012

Smartphone Addiction Recovery Coach for Young Adults (SARC-YA) Experiment

At discharge from outpatient treatment, researchers will recruit 300 young adults and randomly assign them to recovery support as usual control condition or the Smartphone Addiction Recovery Coach for Young Adults (SARC-YA) experimental condition. Participants in the experimental conditions will receive a smartphone, a calling/texting/data plan, and the SARC-YA mobile applications for the first 6 months post treatment discharge. Experimental participants will 1) complete a 2-3 minute recovery-focused ecological momentary assessment (EMA) at 5 random times a day, receive feedback on their current answers, and provided access to behavioral charting of their past answers over time; and 2) receive continuous access to a suite of self-initiated ecological momentary interventions (EMI) to support their recovery via tool box of coping tools, apps related to getting support, and apps related to maintaining a healthy lifestyle. Data include standardized assessments, urine tests, mobile phone metadata, EMA responses, and EMI utilization. The study's primary aim and hypothesis are:

Aim 1: Test the effects of experimental assignment on the frequency of substance use.

H1 Relative to the control group, participants in the experimental group will have lower scores on the quarterly Substance Frequency Scale (3, 6, 9 months post- discharge).

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year–26 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Chestnut Health Systems, Bloomington, Illinois, United States

Loading trial locations.

About this study

At discharge from outpatient treatment, researchers will recruit 300 young adults and randomly assign them to recovery support as usual control condition or the Smartphone Addiction Recovery Coach for Young Adults (SARC-YA) experimental condition. Participants in the experimental conditions will receive a smartphone, a calling/texting/data plan, and the SARC-YA mobile applications for the first 6 months post treatment discharge. Experimental participants will 1) complete a 2-3 minute recovery-focused ecological momentary assessment (EMA) at 5 random times a day, receive feedback on their current answers, and provided access to behavioral charting of their past answers over time; and 2) receive continuous access to a suite of self-initiated ecological momentary interventions (EMI) to support their recovery via tool box of coping tools, apps related to getting support, and apps related to maintaining a healthy lifestyle. Data include standardized assessments, urine tests, mobile phone metadata, EMA responses, and EMI utilization. The study's aims and their associated hypotheses are:

Aim 1: Test the effects of experimental assignment on the frequency of substance use.

H1 Relative to the control group, participants in the experimental group will have lower scores on the quarterly Substance Frequency Scale (3, 6, 9 months post- discharge). Aim 2: Evaluate the extent to which the experimental effects are moderated by baseline substance use frequency. H2 The Substance Frequency Scale Scores at intake will moderate the effects of experimental on the quarterly subsequent Substance Frequency Scale scores. Aim 3: Test the extent to which the frequency of substance use mediates the effects of experimental assignment on other aspects of recovery including SUD symptoms, HIV risk behavior, quality of life, mental wellness, and days of school. H3a Relative to the control group, participants in the experimental group will have better scores on other aspects of recovery (reverse of number of SUD symptoms, reverse of HIV risk behaviors, quality of life, mental wellness, days of school) in the quarterly interviews. H3b Higher Substance Frequency Scale scores (regardless of assignment) in a given quarter will be associated with worse scores on other aspects of recovery in the next quarter. H3c Substance Frequency Scale scores in a given quarter will mediate the impact of the experimental assignment on other aspects of recovery in the next quarter. Aim 4: Within the experimental condition, determine the degree to which EMA responses (e.g., use, withdrawal, craving, negative and positive affect) and EMI utilization predict the duration of abstinence (to be done within experimental condition.) H4a The duration of abstinence will be negatively related to EMA measures of the recency of use, withdrawal, craving, low self-efficacy to resist relapse, increased negative affect, and decreased positive affect. H4b The duration of abstinence will be positively related to immediate and cumulative EMI utilization.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • discharge from an adolescent outpatient SUD treatment program to the community;
  • substance use during the 90 days prior to treatment;
  • aged 18 to 26 at the time of discharge;

Exclusion criteria

  • inability to read and communicate in English;
  • does NOT reside or plan to stay in Chicago during the next 9 months;

Treatment and study plan

Recovery support as usual

Other

same as arm

Smartphone assisted relapse prevention

Other

same as arm

Other names: Relapse Prevention

Primary outcomes

  1. Change in GAIN's Substance Frequency Scale from baseline to 6 months (effect of providing the intervention)

    Time frame: 6 month SFS minus baseline SFS

    The GAIN's Substance Frequency Scale (SFS; alpha=.85; test-retest rho=.94) ranges from 0 to 100% and is calculated as the average percent of days in the past 90 that adolescents reported alcohol, cannabis, stimulates, opioids, and other substance use, days of heavy substance use, and days of problems from substance use. Thus it incorporates the frequency of use, range of substances used, amount used, and degree to which use is causing problems.

Secondary outcomes

  1. Change in GAIN's Substance Frequency Scale from 6 to 9 months (effect of withdrawing the intervention)

    Time frame: 9 months SFS minus 6 month SFS

    The GAIN's Substance Frequency Scale (SFS; alpha=.85; test-retest rho=.94) ranges from 0 to 100% and is calculated as the average percent of days in the past 90 that adolescents reported alcohol, cannabis, stimulates, opioids, and other substance use, days of heavy substance use, and days of problems from substance use. Thus it incorporates the frequency of use, range of substances used, amount used, and degree to which use is causing problems.

  2. Change in GAIN Substance Disorder Screener (SDScr) from baseline to 6 months

    Time frame: 6 month minus baseline

    Count of 5 past 90 day substance use disorder symptoms (alpha=.90) from the GAIN-Q3

  3. Change in GAIN Risk Behavior Screener (RBScr) from baseline to 6 months

    Time frame: 6 month minus baseline

    Count of 6 past 90 day of HIV risk behaviors (test-retest rho=.80) including needle use, needle sharing, unprotected sex, multiple sexual partners, trading sex, and victimization from the GAIN-Q3

  4. Change in European Quality of Life 5 dimensions (EQ5D) from baseline to 6 months

    Time frame: 6 month minus baseline

    Count of 6 quality of life items (alpha=.83) from the EQ5D

  5. Change in Mental Health Continuum Short Form (MHC-SF) from baseline to 6 months

    Time frame: 6 month minus baseline

    Count of 14 items related to mental wellness (alpha=.94) from the MHC-SF

  6. Change in the days of school from baseline to 6 months

    Time frame: 6 month minus baseline

    The days of being in school during the past quarter (test-retest rho=.88) from the GAIN-Q3

  7. Duration of abstinence after a given EMA

    Time frame: Measured at 5 random times per day over 6 months in the experimental condition

    The duration of abstinence is the time from each completed EMA to the next indication of use - measured in days.

Sponsors and collaborators

Lead sponsor

Chestnut Health Systems

Other

Registry information

Acronym: SARC-YA

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
Oct 4, 2017
Registry last updated
Aug 30, 2024

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.