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Comparative Effectiveness of Primary Care-based Interventions for Pediatric ADHD

Comparative Effectiveness of Primary Care-based Interventions for Pediatric ADHD

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02105142
Enrollment
81
Registered
2014-04-07
Start date
2014-04-30
Completion date
2015-09-30
Last updated
2015-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Attention Deficit Hyperactivity Disorder

Keywords

Attention deficit hyperactivity disorder, Interventions, Primary care, Pediatric

Brief summary

Attention-deficit hyperactivity disorder (ADHD) is the most common neurobehavioral disorder of childhood, affecting approximately 8% of youth. Children with ADHD often have problems sustaining attention and completing multi-step commands and tasks of daily living, such as homework. Pediatricians are often the first physicians to identify problems with children's functioning at home and at school. However, because of limited visit time, pediatricians often struggle with managing ADHD while trying to also cover a vast array of other primary care issues. Moreover, as there is a nationwide shortage of pediatric mental health specialists and access to parenting programs is limited, a critical need exists to develop interventions that form partnerships between behavioral and mental health specialists and the primary care pediatrician. One approach is to base interventions in the pediatric clinic to ensure children have access to appropriate treatment. Thus far, only a limited number of sites have this pediatric-mental health partnership. Health information technology (HIT) has been used to enhance primary care management of ADHD. HIT can improve pediatricians' ability not only to adhere to recommended guidelines, but also to screen for co-existing disorders and provide timely parental education. An alternative strategy might be to use group visits (GV). GV afford more time with families and allows the pediatrician to facilitate more in-depth discussions. More importantly, the group model allows parents to learn from one another, normalizes parenting expectations, and addresses shared experiences of medication side effects and other factors related to adherence. Moreover, a group visit can be conducted in a physical location, such as the pediatric clinic, or be brought into the virtual world with the aid of social media. Virtual support groups for chronic care diseases have become an increasingly popular way for a community of individuals to exchange information and offer emotional support. Prior to the adoption of these interventions into primary care practice, investigators must know which is best. Rigorous comparative effectiveness research (CER) can help to determine this. This proposal will compare a HIT based intervention to a GV strategy, with and without the use of social media. These 3 interventions will be compared based not only on clinical measures of interest but also on parent-defined patient outcomes. Prior research has largely focused on measuring clinical outcomes such as treatment adherence and ADHD symptom reduction with little emphasis on understanding how patient-centered outcomes, such as the quality of life of families dealing with ADHD, are affected. Building on previous work, the specific aims for this study are: Aim 1. Compare the preliminary efficacy of three interventions to improve treatment of ADHD in the primary care setting Aim 1a) Compare the effectiveness of the three interventions on clinical measures such as parent and teacher rated ADHD symptoms and adaptive functioning Aim 1b) Compare the effectiveness of the three interventions on patient-centered outcomes such as quality of life and parental satisfaction with the intervention The three interventions will be: 1) Child Health Improvement through Computer Automation (CHICA) which is the health information technology innovation arm; 2) Group visits (GV); or 3) Group visits plus online discussion portal (GV+DP).

Interventions

BEHAVIORALADHD Group Visits

Parents and children attend separate but concurrently run group visits every three months; groups are facilitated by general pediatricians

BEHAVIORALADHD Group Visits plus Online Discussion Portal

Parents and children attend separate but concurrently run group visits every three months; groups are facilitated by general pediatricians. Parent participants will be granted access to the online discussion portal to allow for communication in between in-person group visits.

BEHAVIORALComputer Decision Support

ADHD Module of the Child Health Improvement through Computer Automation (CHICA) system Designed to facilitate physician adherence to clinical care guidelines for ADHD identification and chronic care management

Sponsors

Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED
Indiana University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Children 6 to 12 years of age with diagnosis of ADHD and their parents * Children must receive medical care at participating study clinics * Children must have diagnosis of ADHD based on parent and teacher diagnostic and statistical manual-IV rating scales * Children can have co-existing Oppositional Defiant Disorder (ODD)

Exclusion criteria

* Children with co-existing diagnosis of Conduct Disorder (CD) * Children with autism * Children with moderate to severe mental handicap or other neurodevelopment disorder that would preclude active participation in group discussions

Design outcomes

Primary

MeasureTime frameDescription
Change in Vanderbilt ADHD Rating Scale scoresBaseline & 12 monthsADHD symptoms as measured by parent-report and based on Diagnostic and Statistical Manual-IV diagnostic criteria.

Secondary

MeasureTime frameDescription
Change in scores for pediatric quality of lifeBaseline & 12 monthsQuality of Life (generic core scales): 23 items, related to quality of life and child's needs in context of the family. Parent and child report.
Change in score of multidimensional scale of perceived social support scaleBaseline & 12 monthsSocial Support: 12-items perceptions on support
Parental Locus of Control-Short FormBaselineLocus of Control: 25-items, degree parent feels in control of child behavior
Change in scores related to adaptive functioningBaseline & 12 months13 items, parent-report, measuring adaptive functioning in the home using the Home Situations Questionnaire. Responses at each separate time point will be compared to the study specific Childhood ADHD and Family Impact Scale scores for correlation.
Change in scores on Childhood ADHD & Family Impact ScaleBaseline & 12 monthsStudy-specific tool, 9 items related to common challenges related to parenting based on feedback by patient advisory board

Other

MeasureTime frameDescription
Satisfaction with content of group visitsEvery 3 months at the end of each attended group visitSeparate forms for parent and child feedback on group visits (5-6 items, 1 page); subjects in GV or GV-DP only
Pediatric facilitator feedback formEvery 3 months at the end of each attended group visitParent ratings of communication, teaching style and preparedness of pediatric facilitator; subjects in GV or GV-DP only
Discussion portal feedback form12 monthsClosed and open ended questions about: if parent accessed the online discussion portal (yes/no), how often accessed (daily/weekly/monthly/never), perceived benefits of the online discussion portal, any suggestions for usefulness; subjects in GV-DP only
Adherence to ADHD Group Visit curriculumEvery month for 15 monthsProtocol checklist for each session to be completed by facilitators after each session and by study team to monitor adherence; facilitators and study team only
DemographicsBaselineStudy-specific tool,12 items capturing demographics & characteristics of participant

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026