Electronic Pre-visit Questionnaire to Prompt Discussions of Youth Violence in Primary Care
NCT ID: NCT02041182
Last Updated: 2014-08-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
183 participants
INTERVENTIONAL
2013-10-31
2014-02-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Adolescents ages 13 to 21 who come to the Hasbro Primary Care Clinics for annual physicals will be recruited. A baseline phase was conducted to look at how often providers ask about health-related teen behaviors, assessed by exit survey. The experimental period will involve adolescents completing health-related behavior PVQ, given to their doctor prior to the visit. Exit survey will assess topics discussed. Experimental group will differ from control group based on PVQ containing extra questions about youth violence.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Bullying Prevention Intervention for Adolescent Primary Care Patients
NCT03467009
The Effect of Primary Care Interventions on Children's Media Viewing Habits and Exposure to Violence
NCT01490320
Violence Prevention for Middle School Boys
NCT03109184
Prevention of Violent Behavior Among Children
NCT00056940
Preventing Sexual Violence Through a Comprehensive, Peer-led Initiative
NCT03207386
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention Pre-visit Questionnaire
Adolescents receive PVQ that includes questions about youth violence/bullying
Pre-Visit Questionnaire
Control Pre-visit Questionnaire
Adolescents received PVQ without youth violence/bullying items
Pre-Visit Questionnaire
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pre-Visit Questionnaire
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* presenting for annual physical exam
* provider is general pediatrician (micro-practice 1-8)
* parent present for consent (if under 18 years old)
Exclusion Criteria
* developmental/neurologic delay
* no parent (if under 18 years old)
* presenting for sick visit or specialty clinic
13 Years
21 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Centers for Disease Control and Prevention
FED
HRSA/Maternal and Child Health Bureau
FED
Rhode Island Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Megan Ranney, MD MPH
Role: PRINCIPAL_INVESTIGATOR
Rhode Island Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Hasbro Primary Care Clinics
Providence, Rhode Island, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
APA-YIA-2013
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.