Parents' and Clinicians' Perspectives of the Quick Parenting Assessment (QPA)
NCT ID: NCT04179825
Last Updated: 2024-02-22
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
582 participants
OBSERVATIONAL
2018-12-18
2022-03-04
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Mitigating ACEs in Pediatric Primary Care: Cohort #2 With 6-24 Month Old Children
NCT04160013
Longitudinal Follow-up of Brief Parenting Interventions to Reduce Risk of Child Physical Maltreatment
NCT04059185
Stepped Preventive Care to Reduce the Impact of Acute Pediatric Injury
NCT00451282
Mitigating ACEs in Pediatric Primary Care
NCT03058861
Child-Parent Psychotherapy - a Feasibility Study for Children in Foster Care
NCT04519229
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Efforts are needed to develop and test algorithms that assess for ACEs in pediatric primary care and intervene as indicated.
The investigators have tested an ACEs screening instrument that includes the Quick Parenting Assessment with hundreds of parents of 2-10 year old children in the pediatric primary care clinic at Vanderbilt without incident (please see IRB# 161987).
The next step is a quality improvement (QI) study that integrates an ACEs screening algorithm into pediatric primary care visit.
In this study, the investigators integrate the Quick Parenting Assessment into the pediatric primary care visit at the 15 month, 30 month, 5 year, and 8 year visit. Key measures include parents' and health care providers' perspectives on the new service.
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.
COHORT
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Vanderbilt University Medical Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Seth Scholer
Professor
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Vanderbilt University Medical Center
Nashville, Tennessee, 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.
180956
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.