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CompletedNCT02718508e-ParentingUpdated Apr 11, 2018

An e-Parenting Skills Intervention to Decrease Injured Adolescents' Alcohol Use

An interventional study of eParenting in Parenting and Alcohol Drinking, sponsored by Michael J. Mello, MD, MPH. Completed at 1 site in United States. Open to participants aged 12 Years to 17 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2018-04-11.

Sponsored by Michael J. Mello, MD, MPH · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Sep 2015, registered Mar 2016).
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
12 Years to 17 Years
Sex
All
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Study summary

The objective of this trial is to test feasibility and acceptability of an e-parenting skills intervention with parents of injured adolescent alcohol users (12-17 years old) as compared to standard care at three pediatric trauma centers. To examine these questions, the investigators will randomly assign adolescent and parent dyads (up to 75) to one of two groups. One group will continue to receive the institutional standard care of a brief alcohol intervention delivered by clinical staff to the adolescent with no parenting skills intervention. The second group will continue to receive the same institutional standard care plus the parent will receive an e-parenting skills intervention consisting of: the online parent training program, Parenting Wisely(PW), plus text messaging and a web-based message board. Study participants will be injured adolescents, 12-17 years old, admitted to the inpatient service of the trauma center, and with a positive CRAFFT (mnemonic acronym of first letters of key words in the screening tool) screen for alcohol use. Adolescents' alcohol use will be measured at study enrollment and at 3 and 6 months after discharge. Adolescents' alcohol related negative consequences will be measured at study enrollment for the 6 months prior to hospitalization and again at 6 months after hospital discharge. Parenting skills will also be assessed at 3 and 6 months.

Read the detailed description

This study seeks to test the feasibility and acceptability of an e-parenting skills intervention at three pediatric trauma centers. The investigators will randomize up to 75 dyads of injured adolescents (12-17 years old) who screen positive for alcohol use and their parent to receive either standard trauma center care (a brief intervention with the adolescent) or standard trauma center care (a brief intervention with the adolescent) plus an e-parenting skills intervention consisting of a computerized intervention for parent skill building, a series of text messages and a web-based message board. The primary aim of this study is to determine the feasibility and acceptability of conducting the e-parenting intervention protocol across three pediatric trauma centers in preparation for a larger fully power trial. The central hypothesis for our future fully powered randomized control trial is that adolescents whose parents receive the e-parenting skills intervention will decrease their alcohol use and alcohol-related negative consequences over the 6 months following the intervention more than adolescents who receive only standard trauma center care. Therefore, a secondary aim of this proposal is to calculate a preliminary effect size that could be used, along with other relevant data, such as the acceptability data and findings in the literature, to calculate sample size in a future fully powered randomized control trial. The investigators will also examine adolescent's conjoint use of marijuana. This project advances translational research in collecting preliminary data on an e-parenting skills intervention that can be easily adopted with high fidelity across pediatric trauma centers. Its findings have the potential to directly impact best clinical practices for intervening with alcohol using injured adolescents

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Conditions studied

  • Parenting
  • Alcohol Drinking

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03

In context

Alcohol Drinking

701 studies on the registry are indexed under Alcohol Drinking; 133 are open to participants now.

This study's enrollment of 36 is below the median of 122 across 607 interventional studies indexed under Alcohol Drinking.

Browse Alcohol Drinking studies →

Lead sponsor

This is the only study on the registry with Michael J. Mello, MD, MPH as lead sponsor.

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

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Who can participate

Ages eligible
12 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • adolescents, age 12-17, admitted to the trauma service
  • medically stable
  • a positive CRAFFT screen or lab screen for alcohol use or drug use
  • ability to assent to study and have one parent consent
  • adolescent and parent are English speaking

Exclusion criteria

Exclusion Criteria:

  • the adolescent is cognitively or emotionally unable to participate as determined by a trauma clinician
  • the adolescent is suspected by the clinical staff of being a victim of child abuse (and referred to child protective services)
  • the adolescent is being evaluated following a suicide attempt
  • prior to admission, the adolescent is being treated for an alcohol or drug dependency
  • adolescent is currently incarcerated
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
36 participants (actual)

Study arms

  • No intervention
    Standard Care

    All enrolled adolescents will continue to receive standard trauma center care, a brief intervention during their hospitalization by a trauma center social worker which is required by institutional policy.

  • Experimental
    Standard Care plus e-Parenting Group

    The second group will continue to receive the same institutional standard care plus the parent will receive an e-parenting skills intervention consisting of: the online parent training program, Parenting Wisely (PW), plus text messaging and a web-based message board.

    Behavioral: eParenting

Interventions

  • BehavioraleParenting

    The second group will continue to receive the same institutional standard care plus the parent will receive an e-parenting skills intervention consisting of: the online parent training program, Parenting Wisely (PW), plus text messaging and a web-based message board.

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What researchers measure

Primary outcomes

  1. Feasibility and Acceptability of an e-Parenting Skills Intervention

    Feasibility will be measured by parent data (number of Parenting Wisely logins and activities completed). Acceptability will be measured by the Systems Usability Scale (SUS) which rates parent ease of use of the program and the Consumer Satisfaction Questionnaire (CSQ) which rates level of parent satisfaction with treatment delivery and ability to manage child's behavior.

    Time frame: Up to 3 months

Secondary outcomes

  1. Effects on Alcohol Use as assessed by Adolescent Drug Questionnaire (ADQ).

    Alcohol use will be measured by Adolescent Drug Questionnaire (number of drinking days and heavy drinking days in the past 3 months) among teen participants.

    Time frame: Up to 6 months

  2. Effects on Drug use as assessed by Drug Use Questionnaire (DUQ).

    Drug use will be measured by Drug Use Questionnaire (number of days in the past 3 months teen participants used nicotine, marijuana, cocaine and other drugs).

    Time frame: Up to 6 months

  3. Effects on Alcohol and Drug Related Problems as assessed by Add Health measures.

    Alcohol and drug related problems will be measured by the 9 questions from the Add Health survey (frequency of psychosocial and health consequences associated with alcohol and drug use over the prior 3 month period).

    Time frame: Up to 6 months

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Study locations

1 site
  • Rhode Island Hospital
    Providence, Rhode Island 02903, United States
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References and documents

Individual participant data

Plan to share: No

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 Apr 11, 2018, 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
NCT02718508
Lead sponsor
Michael J. Mello, MD, MPH
Collaborators
Connecticut Children's Medical Center, University of Pittsburgh
Responsible party
Michael J. Mello, MD, MPH (Director, Injury Prevention Center, Rhode Island Hospital) — Sponsor-investigator
First posted
Mar 24, 2016
Start date
Sep 2015
Primary completion
Aug 2017
Completion
Feb 2018
Last update
Apr 11, 2018

Study contacts

Michael J Mello, MD, MPH
principal investigator · Rhode Island Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.

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