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Open Trial of a Program to Support Parents of Children With Attention-deficit/Hyperactivity Disorder (ADHD)

Open Trial of a Program to Support Parents of Children With Attention-deficit/Hyperactivity Disorder in Online Group Meetings

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04636216
Enrollment
14
Registered
2020-11-19
Start date
2020-11-03
Completion date
2021-05-30
Last updated
2021-10-28

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

Conditions

ADHD

Brief summary

Behavioral parent training is an evidence-based treatment for ADHD. The intervention can be implemented individually, or in groups. Currently, group-based parent training programs require considerable coordination, including ascertainment of a large physical space, the coordination of all families traveling to the same location at the same time, and the require for the provision of childcare. Innovations in online connectivity and ease of implementation of online support applications (e.g., Zoom) may reduce these barriers. However, it is necessary to investigate the feasibility and promise of the online approach to ensure it supports parents effectively.

Detailed description

This study will utilize a pre-post, open trial design as the primary aim is to investigate feasibility. Approximately sixty parents will complete prepost ratings of parenting behaviors and measures of child functioning. They will also complete post treatment measures of satisfaction and open-ended questions about feasibility and suggestions for future iterations of the approach. Process measures will include data collection related to attendance and engagement in the activities. Risks include breach of confidentiality and a lack of effectiveness of the intervention for the child's presenting problems. Benefits include the parent receiving an effective intervention.

Interventions

BEHAVIORALCOPE parent training

Weekly 1.5 hour parent training meetings for eight weeks

Sponsors

Florida International University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Open, single-group trial

Eligibility

Sex/Gender
ALL
Age
5 Years to 13 Years
Healthy volunteers
No

Inclusion criteria

* ADHD diagnosis * Intelligence Quotient (IQ) greater than or equal to 70 * At least 1 parent/guardian who can attend zoom sessions * Access to reliable internet connection for zoom meetings

Exclusion criteria

* Evidence of psychosis, suicidal behaviors, or autism level 2/3

Design outcomes

Primary

MeasureTime frameDescription
Observations of parenting behaviors during parent-child interaction8 weeksDyadic Parent Child Interaction code frequency counts for the categories of Negative Talk, Praise, and Commands
Impairment Rating Scale8 weeksAverage score across domains with scores ranging from 0 (No problem) to 6 (Extreme problem)

Countries

United States

Outcome results

None listed

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