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Augmenting Parent Management Training for Child Temper Outbursts Using a Digital Tool

17. September 2026 aktualisiert von: National Institute of Mental Health (NIMH)

Augmenting Parent Management Training With Naturalistic Skills for Child Temper Outbursts Using a Digital Tool

Background:

Pediatric disruptive behavior disorders (DBDs) are characterized by severe irritability, anger, and temper outbursts. The primary way to treat children with DBDs is parent management training (PMT). PMT teaches parents how to reward desired behaviors and not to reward undesired ones. Researchers want to find out if a smartphone app can help parents apply these skills more effectively.

Objective:

To test a smartphone app to enhance PMT.

Eligibility:

Children aged 8 to 13 years with DBDs. A parent or guardian is also needed.

Design:

Parents will have 12 weekly sessions of PMT. PMT teaches them how to manage their child s mood and behaviors. Parents will learn to actively ignore, praise, set limits, and handle temper outbursts. PMT can be either in person or via video. Sessions last 30 to 60 minutes. They will be video and audio recorded.

Parents will be divided into 2 groups. Only 1 group will download a smartphone app. The app helps parents practice PMT skills. It offers videos, a resource library, and alerts when a child may be at risk for various behaviors.

All parents will be prompted every day to answer questions about their child s mood and their own behavior. These will continue until 12 weeks after their last PMT session.

Children will also answer questions on their phone daily for 1 week at a time. They will do this on 3 different weeks, each about 2 months apart. They will also have check-ins by phone every 2 weeks for up to 6 months.

Parents will have follow-up calls 3, 6, and 12 months after they finish PMT.

Studienübersicht

Status

Noch keine Rekrutierung

Bedingungen

Intervention / Behandlung

Detaillierte Beschreibung

Study Description:

This study is a feasibility study (N=60 parent-child dyads) of a digital tool (machine learning and a smartphone application) augmenting parent management training (PMT) to support the reduction of irritability and temper outbursts through changes in parenting behaviors (i.e., active ignoring) for pediatric disruptive behavior disorders (DBDs). We examine the feasibility of the study design (i.e., two-arm randomized controlled trial [RCT] of PMT + ecological momentary assessment [EMA] + digital tool vs. PMT + EMA + no digital tool) and examine patterns of change in irritability, outbursts, and parenting behaviors (i.e., active ignoring).

Objectives:

Primary Objective: Determine the feasibility of the design of a clinical trial (i.e., RCT with two parallel arms - PMT + EMA + digital tool compared to PMT + EMA + no digital tool).

Secondary Objective:

  • Determine whether outbursts and irritability decrease in PMT + EMA + digital tool and PMT + EMA + no digital tool. Determine whether severity of impairment decreases and general functioning improves in both groups.
  • Determine whether active ignoring increases in PMT + EMA + digital tool and PMT + EMA + no digital tool.

Tertiary Objective:

  • Examine whether attention deficit/hyperactivity disorder (ADHD), anxiety, and depression symptoms decrease in PMT + EMA + digital tool and PMT + EMA + no digital tool.
  • Monitor treatment acceptability and fidelity and therapeutic support.

Endpoints:

Primary Endpoint:

Dropout in each arm of the trial (PMT + EMA + digital tool vs. PMT + EMA + no digital tool).

Secondary Endpoint:

  • Changes in child outbursts and irritability measured using the Clinician-rated Affective Reactivity Index (CLARI); parent-/child-ARI; Brief Irritability Test (BITe); and parent/child EMA (collected 3x/day from baseline through 3 months post-treatment). Changes in severity of impairment and general functioning using the Children s Global Assessment Scale (CGAS), Clinical Global Impressions Scale-Severity (CGI-S), and Clinical Global Impress Scale-Improvement (CGI-I).
  • Changes in active ignoring measured using parent EMA (collected 3x/day from baseline through 3 months post-treatment).

Tertiary Endpoint:

  • Changes in symptoms of ADHD, anxiety, and depression. ADHD is measured using the ADHD Rating Scale (ADHD-RS) and Conners Parent Rating Scale (CPRS-R). Anxiety is measured using the Screen for Child Anxiety Related Disorders (SCARED) and Pediatric Anxiety Rating Scale (PARS). Depression is measured using the Mood and Feelings Questionnaire (MFQ) and Child Depression Rating Scale (CDRS).
  • We will monitor treatment acceptability using the Working Alliance Inventory (WAI) and treatment fidelity using an adherence scale previously developed by our group.

Studientyp

Beobachtungs

Einschreibung (Geschätzt)

200

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Maryland
      • Bethesda, Maryland, Vereinigte Staaten, 20892
        • National Institutes of Health Clinical Center
        • Kontakt:
          • NIH Clinical Center Office of Patient Recruitment (OPR)
          • Telefonnummer: TTY dial 711 800-411-1222
          • E-Mail: ccopr@nih.gov

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind

Akzeptiert gesunde Freiwillige

Nein

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

This study is for children 8-13 years old with irritability as a primary clinical concern and no more than minimal response to current treatment. At least one parent/guardian must be willing to enroll and have the cognitive ability to consent, and the child must be able to understand and willing to sign a written assent document. The enrolled, consented parent must be willing to attend 12 parent management training sessions and use the study s digital tool. Both parent and child must be fluent in English. Exclusion criteria for children are active major depression or history of psychosis, bipolar I disorder, level 2 or 3 autism spectrum disorder, active severe substance use, active suicidal intent or plan, IQ below 70, or medical or neurological conditions that may interfere with study participation. Exclusion criteria for parents are IQ below 70, medical/mental health conditions that interfere with participation, or current substance or alcohol problems requiring separate treatment.

Beschreibung

  • INCLUSION CRITERIA:

Inclusion Criteria for Youth:

To be eligible to participate, an individual must be enrolled in the 01-M-0254 protocol. All screening will occur under 01-M-0254 and all inclusion criteria for youth and parent or guardian will be determined under the 01-M-0254 protocol. To be eligible to participate, an individual must meet all the following criteria:

  • Enrollment into protocol 01-M-0254 for screening purposes
  • Age 8-13 years (8 years 0 months through 13 years 11 months)
  • Parent/guardian and/or child reports irritability as a primary clinical concern. Specifically, compared to his/her peers, the child exhibits markedly increased reactivity to negative emotional stimuli that is manifest verbally or behaviorally. For example, the child responds to frustration with extended temper tantrums (inappropriate for age and/or precipitating event), verbal rages, and/or aggression toward people or property. This criterion is assessed based on the clinical interview conducted with parent/guardian and child after consenting into protocol 01-M-0254 for screening.
  • On the basis of record review and interviews with child and parent or guardian, the research team agrees that the child s response to his/her current treatment is no more than minimal (i.e., CGI-S of 3 or more). This criterion is assessed based on the clinical interview conducted with parent/guardian and child after consenting into protocol 01-M-0254 for screening.
  • Patients must be fluent in (speaking, reading) English after consenting into protocol 01-M-0254 as determined through clinical judgement.

    --This study uses English-language manualized PMT. The PMT intervention materials, digital tool, therapist and rater training and supervision procedures, fidelity ratings, and outcome measures are currently available and validated only in English. Because psychotherapy relies on nuanced verbal exchange, use of translation or interpreters could alter treatment content, affect therapeutic alliance, compromise fidelity, and limit accurate clinical risk assessment. Enrolling non-English speakers can introduce a confound to our research objectives around feasibility, symptom and behavior change, and acceptability and fidelity. Restricting enrollment to English-speaking participants is therefore necessary to ensure participant safety and scientific validity in this trial. Critically, this eligibility criterion is based solely on the language requirements of the intervention and study procedures and is not intended to exclude participants on the basis of race or ethnicity or any other factors.

  • At least one parent or guardian of the minor subject must be willing to enroll in the protocol and have the cognitive ability to consent.
  • The minor subject must be able understand a written assent document as determined through clinical judgement, as well as be willing to sign a written assent document.

Inclusion Criteria for Parent or Guardian:

To be eligible to participate, an individual must be enrolled in the 01-M-0254 protocol. All screening will occur under 01-M-0254 and all inclusion criteria for youth and parent or guardian will be determined under the 01-M-0254 protocol. To be eligible to participate, an individual must meet all the following criteria:

  • Enrollment into 01-M-0254 for screening purposes
  • Parent or guardian of a child eligible for this protocol that can attend 12 PMT sessions and is willing to use the digital tool
  • Fluent in English after consenting into protocol 01-M-0254 as determined through clinical judgement
  • Ability of parent or guardian to understand the consent form and the willingness to sign a written informed consent document

EXCLUSION CRITERIA:

Exclusion Criteria for Youth:

All screening will occur under 01-M-0254 and all exclusion criteria for youth and parent or guardian will be determined under the 01-M-0254 protocol. Participants will be screened to exclude participants who would not be able to engage in psychotherapy. All individuals meeting any of the exclusion criteria at baseline will be excluded from participation.

  • Active major depressive disorder or history of psychosis, bipolar I disorder, Level 2 or 3 autism spectrum disorder, active severe substance use disorders (within the last month), have active suicidal intent or plan as detected on screening instruments
  • IQ < 70
  • Past or present medical or neurological condition, disease, disorder, genetic finding, or injury that, in the opinion of the Investigator, may significantly increase the potential risks of study participation, reduce or compromise a subject s ability to fully comply with all study requirements for the duration of the study or may compromise the integrity of the data.

Exclusion Criteria for Parent or Guardian:

All screening will occur under 01-M-0254 and all exclusion criteria for youth and parent or guardian will be determined under the 01-M-0254 protocol. Participants will be screened to exclude participants who would not be able to engage in psychotherapy. All individuals meeting any of the exclusion criteria at baseline will be excluded from participation.

  • IQ < 70 as assessed via a neuropsychological assessment or via assessment by trained clinical staff
  • Have any serious medical, mental health, or any condition that interferes with participation, such as active psychosis.
  • Current alcohol or substance use or dependence (excluding nicotine) within the past 3 months of sufficient magnitude to require independent, concurrent treatment intervention (e.g., antabuse or opiate treatment but not including self-help groups).

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Kohorten und Interventionen

Gruppe / Kohorte
Intervention / Behandlung
Children/adolescents with irritability
Parents/guardians of children/adolescents with irritability
Either parent management training alone or parent management training with a digital tool.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Dropout in each arm of the trial
Zeitfenster: By parent management training session 12
Differential participant dropout in Group 1 (parent management training + digital tool) compared to Group 2 (parent management training + no digital tool) by parent management training session 12.
By parent management training session 12

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Clinician Affective Reactivity Index (CL-ARI)
Zeitfenster: Pre-treatment, bi-weekly during treatment, mid-treatment, post-treatment, follow up (3-, 6-, and 12-months)
A 12-item clinician-administered measure of temper outbursts, irritable mood, and impairment over the past week, based on parent and child report.
Pre-treatment, bi-weekly during treatment, mid-treatment, post-treatment, follow up (3-, 6-, and 12-months)
Affective Reactivity Index (ARI)
Zeitfenster: Pre-treatment, weekly during treatment, mid-treatment, post-treatment
A brief parent- and self-report measure of irritability with 6 core items (score range 0 12) and an additional impairment item not included in the total score.
Pre-treatment, weekly during treatment, mid-treatment, post-treatment
Brief Irritability Test (BITe)
Zeitfenster: Pre-treatment, mid-treatment, post-treatment
A 5-item self-report measure assessing irritability over the past two weeks on a 6-point scale.
Pre-treatment, mid-treatment, post-treatment
Clinical Global Impressions Improvement (CGI-I)
Zeitfenster: Pre-treatment, mid-treatment, post-treatment, follow up (3-, 6-, and 12-months)
A clinician-rated, diagnosis-independent measure of overall treatment response, assessing change from relative to a baseline on a 7-point scale (1 = very much improved to 7 = very much worse).
Pre-treatment, mid-treatment, post-treatment, follow up (3-, 6-, and 12-months)
Clinical Global Impressions Severity (CGI-S)
Zeitfenster: Pre-treatment, bi-weekly during treatment, mid-treatment, post-treatment, follow up (3-, 6-, and 12-months)
A clinician-rated measure of the patient s current level of psychopathology on a 7-point Likert scale ranging from 1 (Normal, not at all ill) to 7 (Among the most extremely ill patients), providing a single global index of illness severity at the time of assessment.
Pre-treatment, bi-weekly during treatment, mid-treatment, post-treatment, follow up (3-, 6-, and 12-months)
The Children s Global Assessment Scale (CGAS)
Zeitfenster: Pre-treatment, bi-weekly during treatment, mid-treatment, post-treatment, follow up (3-, 6-, and 12-months)
A clinician rated, diagnosis nonspecific measure of overall functioning in children and adolescents. It provides a single global rating of the child s psychological, social, and school functioning over a specified time period (usually the current level or past week), based on all available clinical information. Scored on a 100 point continuum divided into 10 point descriptive anchor ranges, with scores ranging from 1 (most impaired functioning) to 100 (superior functioning). Higher scores indicate better overall functioning, while lower scores reflect increasing levels of impairment.
Pre-treatment, bi-weekly during treatment, mid-treatment, post-treatment, follow up (3-, 6-, and 12-months)
Ecological momentary assessment (EMA) of child temper outbursts and irritability
Zeitfenster: In both groups, parents/guardians complete EMA 3x/day from a baseline period through 12 weeks post-treatment (up to 30 weeks) and children complete EMA 3x/day for one week pre-, mid-, and post-treatment (3 weeks total)
EMA items are parent-report and child-report of child temper outbursts and irritability.
In both groups, parents/guardians complete EMA 3x/day from a baseline period through 12 weeks post-treatment (up to 30 weeks) and children complete EMA 3x/day for one week pre-, mid-, and post-treatment (3 weeks total)
Ecological momentary assessment (EMA) of parent active ignoring
Zeitfenster: In both groups, parents/guardians complete EMA 3x/day from a baseline period through 12 weeks post-treatment (up to 30 weeks)
EMA items are parent-report of parent use of the active ignoring skill.
In both groups, parents/guardians complete EMA 3x/day from a baseline period through 12 weeks post-treatment (up to 30 weeks)

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Ermittler

  • Hauptermittler: Melissa A Brotman, Ph.D., National Institute of Mental Health (NIMH)

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

23. September 2026

Primärer Abschluss (Geschätzt)

31. Dezember 2036

Studienabschluss (Geschätzt)

31. Dezember 2037

Studienanmeldedaten

Zuerst eingereicht

13. August 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

13. August 2026

Zuerst gepostet (Tatsächlich)

14. August 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

18. September 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

17. September 2026

Zuletzt verifiziert

8. September 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • 10002714
  • 002714-M

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

JA

Beschreibung des IPD-Plans

In compliance with current NIH data-sharing policies, de-identified data from participants who have consented to data sharing will be made available in a public repository.

IPD-Sharing-Zeitrahmen

De-identified data from participants who have consented to data sharing will be made available in a public repository at time of publication without an end date.

IPD-Sharing-Zugriffskriterien

De-identified data from participants who have consented to data sharing will be made available in a public repository that can be accessed by anyone.

Art der unterstützenden IPD-Freigabeinformationen

  • STUDIENPROTOKOLL
  • ICF
  • ANALYTIC_CODE

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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