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Bullying Prevention Intervention for Adolescent Primary Care Patients

NCT03467009 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 77

Last updated 2019-11-26

No results posted yet for this study

Summary

The purpose of this randomized controlled study is to evaluate acceptability and feasibility, and to gather preliminary data about efficacy, of "iPACT" (intervention to Prevent Adolescent Cyber-victimization with Text messages), a brief in-clinic introductory session + longitudinal automated text-message-based secondary prevention program for adolescents with a history of past-year cyber-victimization presenting to a pediatric clinic for well-child visits.

Conditions

  • Cyberbullying

Interventions

BEHAVIORAL

iPACT Intervention

Brief in-person + tailored, daily 8-week text-message secondary prevention intervention.

OTHER

Control: Enhanced Usual Care (EUC)

EUC group participants will receive standardized information on cyberbullying.

BEHAVIORAL

iPACT Intervention- app

Brief in-person + tailored, daily 8-week message secondary prevention intervention delivered via app.

Sponsors & Collaborators

  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    collaborator NIH

  • Rhode Island Hospital

    lead OTHER

Principal Investigators

  • Megan L Ranney, MD MPH · Rhode Island Hospital

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
13 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-06
Primary Completion
2019-06-12
Completion
2019-07-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03467009 on ClinicalTrials.gov