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CompletedNCT01367847TE-HNCUpdated Sep 11, 2019Results posted

Technology-Enhanced Helping the Noncompliant Child

An interventional study of Helping the Noncompliant Child (HNC) and Technology-Enhanced Helping the Noncompliant Child (TE-HNC) in Child Externalizing Behavior, sponsored by University of North Carolina, Chapel Hill. Completed at 1 site in United States. Open to participants aged 3 Years to 8 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-09-11.

Sponsored by University of North Carolina, Chapel Hill · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
22
Allocation
Randomized
Ages
3 Years to 8 Years
Sex
All
01

Study summary

This study aimed to examine if technology could enhance the treatment engagement and outcomes of low income parents of 3 to 8 children with externalizing problems.

Read the detailed description

The aim of this pilot study is to determine whether a technology-enhanced version of an established behavioral treatment protocol, Helping the Noncompliant Child (HNC; McMahon \& Forehand), enhances the engagement and treatment outcomes of lower income parents of 3 to 8 children with externalizing problems in treatment. It is predicted that families in both the HNC and technology-enhanced HNC (TE-HNC) programs will evidence significant improvement in parenting behavior and child externalizing problems; however, it is predicted that parent-child dyads in the TE-HNC program will require fewer sessions, will be more likely to be retained in the program, will be more likely to remain engaged in the program (e.g., practicing skills between sessions etc.), and will be more likely to have active involvement from their coparenting partners (i.e., other adults and family members who participate in childrearing).In turn, it is expected that the TE-HNC program will boost treatment outcomes.

02

Conditions studied

  • Child Externalizing Behavior

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Keywords

  • Parenting
  • Parent-Child Relations
  • Child Behavior
03

In context

Child Behavior

64 studies on the registry are indexed under Child Behavior; 20 are open to participants now.

This study's enrollment of 22 is below the median of 184 across 61 interventional studies indexed under Child Behavior.

Browse Child Behavior studies →

Lead sponsor

University of North Carolina, Chapel Hill is the lead sponsor of 1,366 studies on the registry; 133 are open to participants now.

Of its 158 completed or terminated interventional studies of FDA-regulated products, 139 (88%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Years to 8 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Lower income
  • caregiver/parent is legal guardian
  • 3 to 8 year old child
  • child meets criteria for externalizing disorder or significant externalizing symptoms

Exclusion criteria

Exclusion Criteria:

  • Prior report of child abuse or neglect
  • current substance abuse/dependence
  • legal guardian reading level less than 8th grade
  • child has developmental disability that precludes caregiver utilizing the skills
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
22 participants (actual)

Study arms

  • Active comparator
    Helping the Noncompliant Child (HNC)

    Standard HNC (see HNC Arm/Title) Program plus Technology-Enhancement (smartphones, which are being used for mid-week video calls to check-in re: skill-building, videotaping of family practice of skills at home, daily surveys re: skills practice \& child behavior, reminders re: practice \& sessions.

    Behavioral: Helping the Noncompliant Child (HNC)

  • Experimental
    Technology-Enhanced HNC (TE-HNC)

    Standard HNC (see HNC Arm/Title) Program plus Technology-Enhancement (smartphones, which are being used for mid-week video calls to check-in re: skill-building, videotaping of family practice of skills at home, daily surveys re: skills practice \& child behavior, reminders re: practice \& sessions.

    Behavioral: Technology-Enhanced Helping the Noncompliant Child (TE-HNC)

Interventions

  • BehavioralHelping the Noncompliant Child (HNC)

    Well-established behavioral parent training program (McMahon \& Forehand) for parents of 3 to 8 y.o. children with externalizing problems

    Also known as: HNC

  • BehavioralTechnology-Enhanced Helping the Noncompliant Child (TE-HNC)

    Standard HNC program plus technology-enhancements (see description under Arm)

    Also known as: TE-HNC

06

What researchers measure

Primary outcomes

  1. Retention

    Retention assesses whether or not the family completed the full treatment program.

    Time frame: Baseline to Post-Intervention (average 8 to 12 weeks)

  2. Mean % Sessions Attended as Scheduled

    Participation in each weekly session as scheduled was recorded for each family. Mean attendance of scheduled sessions was computed for each parent-child dyad and then for each group. For example, if a parent-child dyad required 8 sessions to master the program skills and attended all 8 sessions as scheduled they would have 100%. If instead, another parent-child dyad also required 8 sessions to complete the program, but half of those were rescheduled at least once. Then the overall average attendance is calculated across the parent-child dyads in each group. Greater scheduled attendance = optimal outcome.

    Time frame: Baseline to Post-Intervention (average 8 to 12 weeks)

Secondary outcomes

  1. Mean Post-treatment Score Eyberg Child Behavior Inventory (ECBI)

    The ECBI is a 36 item measure frequently used in treatment outcome research with young children, as it it reflects problem behavior in this age range and is sensitive to change. Parents rate the frequency of each problem behavior as occurring 0 = never to 7 = always. Scores can range from 0 to 252 with higher scores reflecting greater problem behaviors.

    Time frame: Baseline to Post-Intervention (average 8 to 12 weeks)

  2. Mean Sessions for Complete Treatment

    Mean number of sessions that parent-child dyads in each group required to master the program skills and complete treatment (Fewer sessions to complete treatment considered more cost-effective as parent-child dyads learning skills more efficiently).

    Time frame: Baseline to Post-Intervention (Average 8 to 12 weeks)

  3. Mean Consumer Satisfaction

    Average parent-reported satisfaction with the treatment program on a project-developed consumer satisfaction scale (Possible range = 11 -77; Higher score = greater satisfaction).

    Time frame: Post-Intervention (Average 8 to 12 weeks)

07

Results

Posted Sep 14, 2018
Limitations and caveats
This is a preliminary randomized control trial with a small sample size and limited statistical power and, thus, findings should be interpreted with caution.

Participant flow

Participant flow — Overall Study
MilestoneHelping the Noncompliant ChildTE-HNC
Started109
Completed87
Not completed22
Withdrew: Withdrawal by subject22

Outcome measures

PrimaryRetention

Retention assesses whether or not the family completed the full treatment program.

Time frame:
Baseline to Post-Intervention (average 8 to 12 weeks)
Reported as:
Count of participants · Participants
Retention
ParticipantsHelping the Noncompliant ChildTE-HNC
Retention87
PrimaryMean % Sessions Attended as Scheduled

Participation in each weekly session as scheduled was recorded for each family. Mean attendance of scheduled sessions was computed for each parent-child dyad and then for each group. For example, if a parent-child dyad required 8 sessions to master the program skills and attended all 8 sessions as scheduled they would have 100%. If instead, another parent-child dyad also required 8 sessions to complete the program, but half of those were rescheduled at least once. Then the overall average attendance is calculated across the parent-child dyads in each group. Greater scheduled attendance = optimal outcome.

Time frame:
Baseline to Post-Intervention (average 8 to 12 weeks)
Reported as:
Mean · percentage of scheduled sessions
Mean % Sessions Attended as Scheduled
percentage of scheduled sessionsHelping the Noncompliant ChildTE-HNC
Mean % Sessions Attended as Scheduled90 ± 1197 ± 5
SecondaryMean Post-treatment Score Eyberg Child Behavior Inventory (ECBI)

The ECBI is a 36 item measure frequently used in treatment outcome research with young children, as it it reflects problem behavior in this age range and is sensitive to change. Parents rate the frequency of each problem behavior as occurring 0 = never to 7 = always. Scores can range from 0 to 252 with higher scores reflecting greater problem behaviors.

Time frame:
Baseline to Post-Intervention (average 8 to 12 weeks)
Reported as:
Mean · units on a scale
Mean Post-treatment Score Eyberg Child Behavior Inventory (ECBI)
units on a scaleHelping the Noncompliant ChildTE-HNC
Mean Post-treatment Score Eyberg Child Behavior Inventory (ECBI)91.63 ± 21.2583.00 ± 15.34
SecondaryMean Sessions for Complete Treatment

Mean number of sessions that parent-child dyads in each group required to master the program skills and complete treatment (Fewer sessions to complete treatment considered more cost-effective as parent-child dyads learning skills more efficiently).

Time frame:
Baseline to Post-Intervention (Average 8 to 12 weeks)
Reported as:
Mean · Sessions
Mean Sessions for Complete Treatment
SessionsHelping the Noncompliant ChildTE-HNC
Mean Sessions for Complete Treatment10 (7 to 12)8 (7 to 10)
SecondaryMean Consumer Satisfaction

Average parent-reported satisfaction with the treatment program on a project-developed consumer satisfaction scale (Possible range = 11 -77; Higher score = greater satisfaction).

Time frame:
Post-Intervention (Average 8 to 12 weeks)
Reported as:
Mean · score on a scale
Mean Consumer Satisfaction
score on a scaleHelping the Noncompliant ChildTE-HNC
Mean Consumer Satisfaction56.56 ± 2.4759.83 ± 1.94

Adverse events

Collected over 3 years. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Helping the Noncompliant Child0/10 (0%)0/10 (0%)0/10 (0%)
TE-HNC0/9 (0%)0/9 (0%)0/9 (0%)

Baseline characteristics

22 families enrolled, 3 were therapist practice cases (i.e., 19 remaining for analyses),and 4 were drop-outs, yielding a pilot analysis sample of N = 15

Age, Continuous
Age, Continuous(Years)Helping the Noncompliant ChildTE-HNCTotal
Mean5.75 ± 2.125.57 ± 1.275.67 ± 1.72
Sex: Female, Male
Sex: Female, Male(Participants)Helping the Noncompliant ChildTE-HNCTotal
Female549
Male5510
Race/Ethnicity, Customized
Race/Ethnicity, Customized(Participants)Helping the Noncompliant ChildTE-HNCTotal
Minority (Racial and/or Ethnic)6511
08

Study locations

1 site
  • UNC Chapel Hill
    Chapel Hill, North Carolina 27599, United States
09

References and documents

Publications

  • Jones DJ, Forehand R, McKee LG, Cuellar J, Kincaid C. Behavioral Parent Training: Is There an "App" for That? Behav Ther (N Y N Y). 2010 Apr;33(4):72-77. No abstract available. PubMed 22199418 ↗
  • Jones DJ, Forehand R, Cuellar J, Kincaid C, Parent J, Fenton N, Goodrum N. Harnessing innovative technologies to advance children's mental health: behavioral parent training as an example. Clin Psychol Rev. 2013 Mar;33(2):241-52. doi: 10.1016/j.cpr.2012.11.003. Epub 2012 Dec 4. PubMed 23313761 ↗
  • Forehand R, Jones DJ, Parent J. Behavioral parenting interventions for child disruptive behaviors and anxiety: what's different and what's the same. Clin Psychol Rev. 2013 Feb;33(1):133-45. doi: 10.1016/j.cpr.2012.10.010. Epub 2012 Nov 6. PubMed 23178234 ↗
  • Jones DJ. Future directions in the design, development, and investigation of technology as a service delivery vehicle. J Clin Child Adolesc Psychol. 2014;43(1):128-42. doi: 10.1080/15374416.2013.859082. PubMed 24400723 ↗
  • Jones DJ, Forehand R, Cuellar J, Parent J, Honeycutt A, Khavjou O, Gonzalez M, Anton M, Newey GA. Technology-enhanced program for child disruptive behavior disorders: development and pilot randomized control trial. J Clin Child Adolesc Psychol. 2014;43(1):88-101. doi: 10.1080/15374416.2013.822308. Epub 2013 Aug 7. PubMed 23924046 ↗
  • Loiselle R, Parent J, Georgeson AR, Thissen D, Jones DJ, Forehand R. Validation of the Multidimensional Assessment of Parenting: An application of item response theory. Psychol Assess. 2021 Sep;33(9):803-815. doi: 10.1037/pas0001019. Epub 2021 Apr 26. PubMed 33900099 ↗
  • Jones DJ, Loiselle R, Zachary C, Georgeson AR, Highlander A, Turner P, Youngstrom JK, Khavjou O, Anton MT, Gonzalez M, Bresland NL, Forehand R. Optimizing Engagement in Behavioral Parent Training: Progress Toward a Technology-Enhanced Treatment Model. Behav Ther. 2021 Mar;52(2):508-521. doi: 10.1016/j.beth.2020.07.001. Epub 2020 Jul 15. PubMed 33622517 ↗
  • Zachary C, Jones DJ, McKee LG, Baucom DH, Forehand RL. The Role of Emotion Regulation and Socialization in Behavioral Parent Training: A Proof-of-Concept Study. Behav Modif. 2019 Jan;43(1):3-25. doi: 10.1177/0145445517735492. Epub 2017 Oct 13. PubMed 29029562 ↗
  • Anton MT, Jones DJ, Youngstrom EA. Socioeconomic status, parenting, and externalizing problems in African American single-mother homes: A person-oriented approach. J Fam Psychol. 2015 Jun;29(3):405-415. doi: 10.1037/fam0000086. PubMed 26053349 ↗
  • Parent J, Jones DJ, Forehand R, Cuellar J, Shoulberg EK. The role of coparents in African American single-mother families: the indirect effect of coparent identity on youth psychosocial adjustment. J Fam Psychol. 2013 Apr;27(2):252-62. doi: 10.1037/a0031477. Epub 2013 Feb 11. PubMed 23398615 ↗
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Timeline

Tracking since Sep 25, 2026
Not marked actual or estimatedDates not marked actual or estimated

The record gives a start of Sep 2010, a primary completion of Oct 2012 and a completion of May 2013. It does not say whether these dates are actual or estimated.

Results were first posted in Sep 2018, 5 years 11 months after primary completion.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 1, 2011
First posted
Jun 7, 2011
Start
Sep 2010
Primary completionActual
Oct 2012
CompletionActual
May 2013
Results first posted
Sep 14, 2018
Last update
Sep 11, 2019
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 11, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01367847
Responsible party
Sponsor
First posted
Jun 7, 2011
Start date
Sep 2010
Primary completion
Oct 2012
Completion
May 2013
Results posted
Sep 14, 2018
Last update
Sep 11, 2019

Study contacts

Deborah J Jones, PhD
principal investigator · UNC Chapel Hill

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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