- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06193382
Parent-Child Interaction Therapy (PCIT) for Children With Traumatic Brain Injury (TBI): A Stepped-Care Model
May 7, 2026 updated by: Dainelys Garcia, University of Miami
The purpose of this study is to understand how a stepped-care model of Parent-Child Interaction Therapy (Step-Up PCIT) addresses child behavioral problems among children between the ages of 2 and 7 with a traumatic brain injury (TBI).
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Dainelys Garcia, PhD
- Phone Number: 3052430234
- Email: ngarcia09@med.miami.edu
Study Locations
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Florida
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Miami, Florida, United States, 33136
- University of Miami
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Contact:
- Dainelys Garcia, PhD
- Phone Number: 305-243-0234
- Email: ngarcia09@med.miami.edu
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Principal Investigator:
- Dainelys Garcia, PhD
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Child Inclusion Criteria:
- Child is between the ages of 2 and 7
- Child has a mild to moderate TBI
Primary Caregiver Inclusion Criteria:
- Primary caregiver is 18 years or older
- Primary caregiver speaks and reads in either English or Spanish
Child Exclusion Criteria:
- Children with major sensory impairments (e.g., deafness, blindness)
Primary Caregiver Exclusion Criteria:
- Primary caregiver with major sensory impairments (e.g., deafness, blindness)
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: PCIT Group
Participants in this group will receive the PCIT intervention for up to 5 weeks.
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Participants will receive the adapted Pocket PCIT Online via a web-based learning platform for up to 5 weeks.
Participants will engage in this intervention weekly for about 1 hour per week.
During engaging with the adapted Pocket PCIT Online version of PCIT, caregivers will learn positive parenting skills to increase the warmth of the parent-child relationship as well as strategies to effectively set limits.
Participants will also participate in 15-minute check-in phone calls with a therapist each week throughout the course of treatment.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in child behavior problem frequency and severity as measured by the Eyberg Child Behavior Inventory (ECBI) intensity scale
Time Frame: Baseline and week 5
|
The ECBI questionnaire will be used to evaluate the number of behavioral problems and the frequency of their occurrence before and after the intervention program.
ECBI provides a list of 36 problem behaviors commonly reported by parents.
The inventory assesses behavior on two dimensions: 1) the frequency of the behavior; 2) whether parents consider it a problem.
The frequency ratings range from 1 (never) to 7 (always), and are summed up to arrive at an overall problem behavior Intensity Score, ranging from 36 to 252.
Higher score means more behavioral problems.
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Baseline and week 5
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Change in caregiver-perceived child behavior problems as measured by the Eyberg Child Behavior Inventory (ECBI) problem scale
Time Frame: Baseline and week 5
|
The ECBI questionnaire will be used to evaluate the number of behavioral problems and the frequency of their occurrence before and after the intervention program.
ECBI provides a list of 36 problem behaviors commonly reported by parents.
The inventory assesses behavior on two dimensions: 1) the frequency of the behavior; 2) whether parents consider it a problem.
The frequency ratings range from 1 (never) to 7 (always), and are summed up to arrive at an overall problem behavior Intensity Score, ranging from 36 to 252.
Higher score means more behavioral problems.
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Baseline and week 5
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Change in parent stress as measured by the Parenting Stress Index Fourth Edition Short Form (PSI-SF) total score
Time Frame: Baseline and week 5
|
PSI-4-SF assesses the parents stress level.
PSI-4-SF contains 36 items: 12 items for Parental Stress (PS), 12 items for Parent-Child Dysfunctional Interaction (P-CDI), and 12 items for Difficult Child (DC).The normal range for scores is within the 16th to 84th percentiles.Scores in the 85th to 89th percentile are considered high, and scores in the 90th percentile or higher are considered clinically significant.
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Baseline and week 5
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Change in parent stress as measured by the Parenting Stress Index Fourth Edition Short Form (PSI-SF) Parent Stress (PS) score
Time Frame: Baseline and week 5
|
PSI-4-SF assesses the parents stress level.PSI-4-SF contains 36 items: 12 items for Parental Stress (PS) , 12 items for Parent-Child Dysfunctional Interaction (P-CDI), and 12 items for Difficult Child (DC).The normal range for scores is within the 16th to 84th percentiles.Scores in the 85th to 89th percentile are considered high, and scores in the 90th percentile or higher are considered clinically significant.
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Baseline and week 5
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Change in parent-child dysfunctional interaction as measured by the Parenting Stress Index Fourth Edition Short Form (PSI-SF) Parent-Child Dysfunctional Interaction (P-CDI) score
Time Frame: Baseline and week 5
|
PSI-4-SF assesses the parents stress level.PSI-4-SF contains 36 items: 12 items for Parental Stress (PS) , 12 items for Parent-Child Dysfunctional Interaction (P-CDI), and 12 items for Difficult Child (DC).The normal range for scores is within the 16th to 84th percentiles.Scores in the 85th to 89th percentile are considered high, and scores in the 90th percentile or higher are considered clinically significant.
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Baseline and week 5
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Change in how the caregiver perceptions about how it is to care for the child as measured by the Parenting Stress Index Fourth Edition Short Form (PSI-SF) Difficult Child (DC) score
Time Frame: Baseline and week 5
|
PSI-4-SF assesses the parents stress level.PSI-4-SF contains 36 items: 12 items for Parental Stress (PS) , 12 items for Parent-Child dysfunctional Interaction (P-CDI), and 12 items for Difficult Child (DC).The normal range for scores is within the 16th to 84th percentiles.Scores in the 85th to 89th percentile are considered high,and scores in the 90th percentile or higher are considered clinically significant.
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Baseline and week 5
|
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Change in parenting skills as measured by the Dyadic Parent-Child Interaction Coding System-Fourth Edition (DPIC-IV)
Time Frame: Baseline and week 5
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The Dyadic Parent-Child Interaction Coding System-4th Ed is a structured behavioral observation coding system assessing caregiver-child interactions.
Observed parenting behaviors will be coded during a 5-min parent-child play session with a tablet with educational apps and combined into two categories of positive (praises, behavior descriptions, and reflections) and negative (questions, commands, and negative talk) verbalizations, reflecting behaviors caregivers are taught to use and avoid in PCIT.
The higher the score the higher quality the parenting behavior.
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Baseline and week 5
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Treatment satisfaction as measured by the Therapist Attitude Inventory (TAI)
Time Frame: Up to 5 weeks
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TAI is a valid index of consumer satisfaction for participants in behavioral parent training (BPT).
Items are rated on a scale from one (indicating treatment dissatisfaction or lack of improvement) to five (indicating satisfaction with treatment and improvement).
Parents will complete this form after the last session of the BPT program.
BPT consists of 11 items that are scored on a 5-point Likert scale.
The total score range is 11-55; the higher the score, the greater the satisfaction
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Up to 5 weeks
|
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Number of modules completed by the caregiver
Time Frame: Up to 5 weeks
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Number of modules completed by the caregiver
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Up to 5 weeks
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Number of week homework was completed by the caregiver
Time Frame: Up to 5 weeks
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Number of week homework was completed by the caregiver
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Up to 5 weeks
|
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Acceptability of Intervention Measure (AIM)
Time Frame: Up to 5 weeks
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The Likert scale has 4 items.
The scores will be summed to provide a total score.
Scores range from completely disagree to completely agree.
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Up to 5 weeks
|
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Intervention Appropriateness Measure (IAM)
Time Frame: Up to 5 weeks
|
The Likert scale has 4 items.
The scores will be summed to provide a total score.
Scores range from completely disagree to completely agree.
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Up to 5 weeks
|
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Feasibility of Intervention Measure (FIM)
Time Frame: Up to 5 weeks
|
The Likert scale has 4 items.
The scores will be summed to provide a total score.
Scores range from completely disagree to completely agree.
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Up to 5 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in family functioning as measure by the General Functioning (GF) Scale
Time Frame: Baseline and week 5
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The general functioning scale is made up of 12 items with six items that reflect healthy family functioning and the other six items reflecting unhealthy functioning.
Scoring is on a 4-point scale (from 1 for strongly agree to 4 for strongly disagree) with the scoring for the negatively worded items reversed.
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Baseline and week 5
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Change in child's functioning as measured by the Strengths and Difficulties Questionnaire (SDQ)
Time Frame: Baseline and week 5
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SDQ is a brief emotional and behavioral screening questionnaire for children and young people.
Scores range from minimal value (not true) to maximum value (certainly true).The scores will be summed to provide a total score.
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Baseline and week 5
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Change in child's emotional symptoms as measured by the Strengths and Difficulties Questionnaire (SDQ) emotional symptoms scale
Time Frame: Baseline and week 5
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SDQ is a brief emotional and behavioral screening questionnaire for children and young people.
Scores range from minimal value (not true) to maximum value (certainly true).The scores will be summed to provide a total score.
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Baseline and week 5
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Change in child's conduct problems as measured by the Strengths and Difficulties Questionnaire (SDQ) conduct problems scale
Time Frame: Baseline and week 5
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SDQ is a brief emotional and behavioral screening questionnaire for children and young people.
Scores range from minimal value (not true) to maximum value (certainly true).The scores will be summed to provide a total score.
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Baseline and week 5
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Change in child's hyperactivity/inattention as measured by the Strengths and Difficulties Questionnaire (SDQ) hyperactivity/inattention scale
Time Frame: Baseline and week 5
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SDQ is a brief emotional and behavioral screening questionnaire for children and young people.
Scores range from minimal value (not true) to maximum value (certainly true).The scores will be summed to provide a total score.
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Baseline and week 5
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Change in child's peer relationship problems as measured by the Strengths and Difficulties Questionnaire (SDQ) peer relationship problems scale
Time Frame: Baseline and week 5
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SDQ is a brief emotional and behavioral screening questionnaire for children and young people.
Scores range from minimal value (not true) to maximum value (certainly true).The scores will be summed to provide a total score.
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Baseline and week 5
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Change in child's prosocial behaviors as measured by the Strengths and Difficulties Questionnaire (SDQ) prosocial behavior scale
Time Frame: Baseline and week 5
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SDQ is a brief emotional and behavioral screening questionnaire for children and young people.
Scores range from minimal value (not true) to maximum value (certainly true).The scores will be summed to provide a total score.
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Baseline and week 5
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Dainelys Garcia, PhD, University of Miami
- Principal Investigator: Jason F Jent, PhD, University of Miami
- Principal Investigator: Jennifer Coto, PhD, University of Miami
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
November 1, 2026
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
January 30, 2027
Study Registration Dates
First Submitted
December 21, 2023
First Submitted That Met QC Criteria
December 21, 2023
First Posted (Actual)
January 5, 2024
Study Record Updates
Last Update Posted (Actual)
May 12, 2026
Last Update Submitted That Met QC Criteria
May 7, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20230405
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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