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NCT05301933

Telehealth BPT in DBP Practice

Completed NA Last updated 18 November 2023
What this trial tests

NA trial testing Behavioral Parent Training (BPT) in ADHD in 13 participants. Completed in 11 September 2023.

Timeline
1 July 2022
Primary endpoint
1 September 2023
11 September 2023

Quick facts

Lead sponsorNYU Langone Health
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment13
Start date1 July 2022
Primary completion1 September 2023
Estimated completion11 September 2023
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

NYU Langone Health — full company profile →

Who can join

Adults 4 to 11, any sex, with ADHD. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Access to evidence-based psychosocial interventions, particularly Behavioral Parent Training (BPT), for youth with Attention Deficit/Hyperactivity Disorder (ADHD) is limited. An approach to increasing such access is to utilize trained paraprofessionals (Family Peer Advocates; FPAs) in the delivery of BPT, particularly through modalities, like telehealth, that further improve access and availability. This approach, FPA-delivered BPT via telehealth has yet to be studied. This study will evaluate the benefits of a FPA-delivered BPT for parents of children identified with ADHD in Developmental Behavioral Pediatric (DBPs).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Behavioral Parent Training (BPT)

Trials testing the same drug.

Other recruiting trials for ADHD

Currently open trials in the same condition.

Other NYU Langone Health trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05301933.

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