Status:

UNKNOWN

Randomized Controlled Trial of the Myndlift BPT App

Lead Sponsor:

New York University

Collaborating Sponsors:

Myndlift Ltd.

Conditions:

ADHD

Behavioral Disorder

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

We propose addressing these aims by conducting a randomized controlled trial (RCT) that will evaluate the hybrid BPT (Myndlift BPT) compared to a wait-list control group. All participants will receive...

Detailed Description

Over the past several decades, much of the literature on attention-deficit/hyperactivity disorder (ADHD) and other disruptive behavior disorders (DBDs; i.e., conduct disorder/CD and oppositional defia...

Eligibility Criteria

Inclusion

  • the child must be between the ages of 3-11 at the time of baseline/pretreatment data collection;
  • the child must have an elevated score based on parent-report on the Inattention and/or Hyperactivity/Impulsivity Symptom Index of the ADHD Rating Scale- 5 (Dupual et al., 2016)
  • the parent/caregiver must be a fluent English speaker;
  • the parent/caregiver must be the legal guardians of and have full-time child care responsibilities for their child (parents/caregiver with limited contact with their child will not have the opportunity to sufficiently practice the BPT skills),
  • the parent/caregiver must have reliable and stable mobile internet access,
  • the parent/caregiver must use an Apple iOS operating system (Myndlift BPT is only available in iOS 9 or above) the parent/caregiver and their child must reside in the United States.

Exclusion

  • the child or parent/caregiver presents with emergency psychiatric needs that require services beyond those that can be managed within this intervention format (e.g., hospitalization, specialized placement outside the home); In this case, an active intervention by research staff to secure what is needed will be made;
  • if the child has an elevated score for Autism Spectrum Disorder on the Developmental Behavior Checklist-Autism Screening Algorithm (youth with ASD often require considerably more intervention; and,
  • if the parent/caregiver is currently enrolled or has recently enrolled in any type of BPT program (i.e., past two years).

Key Trial Info

Start Date :

January 1 2022

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 30 2022

Estimated Enrollment :

60 Patients enrolled

Trial Details

Trial ID

NCT05182424

Start Date

January 1 2022

End Date

June 30 2022

Last Update

January 10 2022

Active Locations (1)

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1

New York University

New York, New York, United States, 10003