Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02145793 · ClinicalTrials.gov registry record · NA

Exploring the Group Visit Model for Pediatric ADHD Management in the Medical Home

A NA study, sponsored by Indiana University.

Completed
Registry status
NA
Development phase
56
Enrollment target

NCT02145793: Completed NA study, sponsored by Indiana University.

NCT02145793 is a NA study that has completed, run by Indiana University. The registered enrollment target is 56 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02145793, a NA study, has completed, sponsored by Indiana University.

COMPLETED
Registry status
NA
Development phase
56 participants
Enrollment target

Study Summary

Attention deficit hyperactivity disorder (ADHD) affects 8% of US youth. Even though evidence shows medications are effective in reducing ADHD symptoms, many families experience ongoing parenting stress around parent-child interactions. Children often have ongoing impairments in functioning. ADHD is a common condition identified and managed by primary care pediatricians. However current care in the clinic is not optimal to address parents' and children's needs around ADHD chronic care. Time is the biggest barrier. Group visits are a viable option to improve pediatric ADHD care, but requires extensive study. The goal of this proposed study is to test the feasibility and effectiveness of the group visit model for ADHD management within pediatric primary care. This study will be a randomized feasibility study that will generate important pilot data, as well as result in an innovative, exportable pediatric ADHD group curriculum for primary care practice.

Primary Outcome

Feasibility of group visit model was measured as number of visits to the clinic by chart review. We also looked at the number of group visits a family attended based on the sign in sheet provided at the beginning of each session.

Interventions

  • BEHAVIORAL ADHD Group Curriculum

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2012-06
Est. Completion 2013-11
Phase NA
Indiana University

890 total trials

What the finished NCT02145793 record still lists

NCT02145793 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 56 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 1 intervention - of which ADHD Group Curriculum is the first listed.

NCT02145793 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02145793 about?

NCT02145793 is a clinical study titled "Exploring the Group Visit Model for Pediatric ADHD Management in the Medical Home". Attention deficit hyperactivity disorder (ADHD) affects 8% of US youth. Even though evidence shows medications are effective in reducing ADHD symptoms, many families experience ongoing parenting stress around parent-child interactions. Children often have ongoing impairments in functioning. ADHD is ...

What is the current status of trial NCT02145793?

This trial is currently completed. It is a NA study. The enrollment target is 56 participants. The study started on 2012-06. Estimated completion is 2013-11.

What interventions are being tested in trial NCT02145793?

The interventions under investigation include: ADHD Group Curriculum (BEHAVIORAL).

Who is sponsoring clinical trial NCT02145793?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02145793's enrollment target sits among peer trials

56 1262nd of 2000 higher than 737 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02287428 · 56 participants · Phase 1

    Personalized NeoAntigen Cancer Vaccine w RT Plus Pembrolizumab for Patients With Newly Diagnosed GBM

  • NCT02923011 · 56 participants · Phase 3

    Comparative Effectiveness of MRgFUS Versus CTgRFA for Osteoid Osteomas

  • NCT02935283 · 56 participants

    Neuroimaging and Neuropsychological Outcomes in Urea Cycle Disorders

  • NCT03375866 · 56 participants · NA

    Effects of Mixed Nut Consumption on Satiety and Weight Management

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02145793, the US trial registry maintained by the National Library of Medicine. NCT02145793 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.