- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05400434
Natural Helpers and PCIT
January 11, 2026 updated by: Jason Jent, University of Miami
The Development and Implementation of a Natural Helpers Program to Increase the Recruitment, Retention, and Engagement of Underserved Families in Parent-Child Interaction Therapy (PCIT)
The purpose of the study is to evaluate the effect of a time-limited (i.e., 18 weeks) community health worker (CHW) intervention, referred to as the Parent Child Interaction Therapy (PCIT) plus natural helper (NH) model, on treatment engagement, retention, and child and caregiver outcomes.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Estimated)
300
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 Contact Backup
- Name: Natalie Espinosa, PsyD
- Phone Number: 3052430234
- Email: nae30@med.miami.edu
Study Locations
-
-
Florida
-
Miami, Florida, United States, 33136
- Recruiting
- ConnectFamilias
-
Principal Investigator:
- Jason Jent, PhD
-
Contact:
- Betty Alonso
- Phone Number: 3058542973
- Email: betty@connectfamilias.org
-
Miami, Florida, United States, 33136
- Recruiting
- Mailman Center for Child Development
-
Contact:
- Dainelys Garcia, PhD
- Phone Number: 3052430234
- Email: ngarcia09@med.miami.edu
-
Principal Investigator:
- Jason Jent, PhD
-
-
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
2 years to 12 years (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Families of children 2 years of age to 12 years of age.
- Children 2 to 7 years of age with a history of child abuse or neglect and/or child behavior problems or children ages 8 years to 12 years of age with history of or risk for abuse and the child does not exhibit clinically significant behavior problems.
- At the time of enrollment, participants must agree that, within the upcoming six months, they will not move away to a location where they would no longer be able to regularly attend weekly sessions (i.e., moving out of Miami Dade County).
Exclusion Criteria:
- Families with child younger than 2 years of age or older than 7 years of age with clinically significant behavior problems
- Adults who are unable to consent and prisoners
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Randomized Standard-PCIT group
Participants enrolled in the randomized portion of the study and randomized to receive only Standard PCIT for a maximum of 18 weeks.
|
PCIT is an evidence-based behavioral parenting intervention.
It is administered as weekly, one-hour sessions with a bilingual PCIT therapist for 18 weeks in one of three PCIT clinics embedded within neighborhood community agencies or virtually.
|
|
Experimental: Randomized PCIT plus Natural Helper group
Participants enrolled in the randomized portion of the study and randomized to receive PCIT plus Natural Helper for a maximum of 18 weeks.
|
PCIT is an evidence-based behavioral parenting intervention.
It is administered as weekly, one-hour sessions with a bilingual PCIT therapist for 18 weeks in one of three PCIT clinics embedded within neighborhood community agencies or virtually.
Natural helpers are lay people to whom others naturally turn for advice, emotional support, and tangible aid.
Families received weekly sessions with a natural helpers in their home or virtually for 30-45 minutes for a maximum of 18 weeks.
During sessions, natural helpers work with families to (1) explain parenting principles in a culturally and responsive manner; (2) support them in their skill acquisition; and (3) troubleshoot structural barriers to service and other basic life needs.
|
|
Experimental: Opt-out Only Standard PCIT group
Participants enrolled in the non-randomized portion of the study and opted in to receive only Standard PCIT for a maximum of 18 weeks.
|
PCIT is an evidence-based behavioral parenting intervention.
It is administered as weekly, one-hour sessions with a bilingual PCIT therapist for 18 weeks in one of three PCIT clinics embedded within neighborhood community agencies or virtually.
|
|
Experimental: Opt-in PCIT plus Natural Helper group
Participants enrolled in the non-randomized portion of the study and opted in to receive PCIT plus Natural Helper for a maximum of 18 weeks.
|
PCIT is an evidence-based behavioral parenting intervention.
It is administered as weekly, one-hour sessions with a bilingual PCIT therapist for 18 weeks in one of three PCIT clinics embedded within neighborhood community agencies or virtually.
Natural helpers are lay people to whom others naturally turn for advice, emotional support, and tangible aid.
Families received weekly sessions with a natural helpers in their home or virtually for 30-45 minutes for a maximum of 18 weeks.
During sessions, natural helpers work with families to (1) explain parenting principles in a culturally and responsive manner; (2) support them in their skill acquisition; and (3) troubleshoot structural barriers to service and other basic life needs.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Child externalizing behavior as measured by ECBI Intensity Scale
Time Frame: Up to 26 weeks
|
The Eyberg Child Behavior Inventory (ECBI) is a 36-item caregiver report measure of disruptive behaviors in children ages 2-16 .
The Intensity Scale assesses the frequency of behavior problems (1=never to 7=always) with total scores ranging from 36 to 252.
A raw score of 131 or higher on the Intensity Scale is considered clinically significant child externalizing behavior.
|
Up to 26 weeks
|
|
Child externalizing behavior as measured by ECBI Problem Scale
Time Frame: Up to 26 weeks
|
The Eyberg Child Behavior Inventory (ECBI) is a 36-item caregiver report measure of disruptive behaviors in children ages 2-16 .
The Problem Scale assesses caregiver perceived behavior problems (1 = yes, 0 = no) with total scores ranging from 0 to 36.
A raw score of 15 or higher on the Problem Scale is considered clinically significant child externalizing behavior.
|
Up to 26 weeks
|
|
Parenting Skills as measured by the Dyadic Parent-Child Interaction Coding System (DPICS-IV)
Time Frame: Up to 26 weeks
|
The DPICS-IV is a behavioral observation tool used to code and assess caregiver behaviors and the quality of caregiver and child interactions.
PCIT therapists code the three 5-minute DPICS-IV observations: (1) child-led play (CLP), (2) parent-led play (PLP), and (3) clean-up (CU).
The number of positive parenting practices (e.g., labeled praises, reflections, and behavior descriptions) and negative parenting practices are tallied (e.g., questions, commands, and criticisms) are coded during CLP observations.
During PLP and CU observations, caregiver verbalizations were coded to generate rates of: (1) caregiver effective commands, (2) caregiver correct follow-through on effective commands, and (3) child compliance to effective commands.
The higher the score the higher the parenting behavior and child compliance.
|
Up to 26 weeks
|
|
Parenting Stress as measured by Parenting Stress Index Short Form (PSI-SF-4)
Time Frame: Up to 26 weeks
|
The PSI-SF-4 is a 36-item self-report questionnaire used to measure caregiver stress and difficulties in the caregiver-child relationship for caregivers of youth between ages 0-12.
The PSI-SF-4 yields a Total Stress percentile score (0-100) with higher scores indicating higher stress.
|
Up to 26 weeks
|
|
Family conflict as measured by Bloom's Family Processes Scale
Time Frame: Up to 26 weeks
|
The Bloom's Family Processes Scale assesses family conflict and cohesion using a 5-item conflict subscale (e.g.
"we fight a lot in our family").
Caregivers rate their level of agreement on a five-point Likert scale (1=strongly agree to 5=strongly disagree).
Total score ranges from 5-25 with the higher scores indicating greater conflict.
|
Up to 26 weeks
|
|
Family cohesion as measured by Bloom's Family Processes Scale
Time Frame: Up to 26 weeks
|
The Bloom's Family Processes Scale assesses family cohesion using a 5-item cohesion subscale (e.g., "there is a feeling of togetherness in our family").
Caregivers rate their level of agreement on a five-point Likert scale (1=strongly agree to 5=strongly disagree).
Total score ranges from 5-25 with the higher scores indicating greater cohesion.
|
Up to 26 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jason Jent, 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 (Actual)
December 3, 2018
Primary Completion (Estimated)
December 27, 2026
Study Completion (Estimated)
December 27, 2026
Study Registration Dates
First Submitted
May 27, 2022
First Submitted That Met QC Criteria
May 27, 2022
First Posted (Actual)
June 1, 2022
Study Record Updates
Last Update Posted (Estimated)
January 13, 2026
Last Update Submitted That Met QC Criteria
January 11, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20140839
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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