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I-InTERACT Preterm

I-InTERACT Preterm

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05282628
Enrollment
19
Registered
2022-03-16
Start date
2021-09-01
Completion date
2026-08-31
Last updated
2024-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pre-Term

Brief summary

Open pilot of a brief online parenting-skills intervention for young children ages 3-8 who were born very preterm (\< 32 weeks gestational age). Parent-child interactions, child behavior, parent functioning, and child white matter connectivity will be assessed pre- and post-intervention 10 weeks later.

Detailed description

The investigators will modify I-InTERACT North to reflect United States language and culture and emphasize our focus on neural plasticity and development. The modified intervention will be renamed Building Better Brains and Behavior (B4 Preterm). Then, investigators will conduct a single-arm clinical trial to establish B4 Preterm's feasibility, acceptability and preliminary efficacy in improving child and family outcomes. Additionally, neuroimaging (MRI/DTI) will be collected pre- and post-intervention. The primary neuroimaging sequence will allow the investigators to examine associations between white matter injury and treatment response as well as changes in neural activation and connectivity pre- to post-treatment. An exploratory neuroimaging sequence will also be collected pre- and post-intervention. This exploratory sequence will serve as a backup for the primary sequence in case it is affected by significant motion and allow the investigators to test this sequence in young children.

Interventions

BEHAVIORALBuilding Better Brains and Behavior program (B4 Preterm)

The program couples online learning modules with video conferencing sessions with a trained therapist to review skills and practice implementing the skills with live coaching. Online modules include didactic content, video clips of parents modeling the skills, and exercises. Parents will complete intervention modules sequentially in conjunction with scheduled 1:1 videoconference sessions with a trained therapist. Videoconference sessions with the therapist will be scheduled weekly, once parents have completed their modules. During these sessions, the therapist will review the online materials and provide active coaching to the parent on how to use the skills with their child (e.g., labeled praise, reflective responses). Each session follows a manualized therapy protocol to optimize content fidelity. Parents will be instructed to practice the parenting skills for 5 minutes each day to promote mastery in the home environment.

Sponsors

Children's Hospital Medical Center, Cincinnati
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
36 Months to 96 Months
Healthy volunteers
No

Inclusion criteria

* Age at enrollment: ages 3-8, inclusive * Born at \< 32 weeks gestational age * Total T score of \> 55 on the Child Behavior Checklist Total or Externalizing Behavior Scales OR Total T score of \> 55 on the Eyberg Child Behavior Inventory total problem- or total intensity-scale OR documented behavioral problems noted in medical chart and parent endorses current concerns about child's behaviors * Language: English must be the primary spoken language in the home

Exclusion criteria

Caregiver must be 18 years or older to participate in the intervention. Participant will be excluded from the study if the child does not reside with the caregiver at least half-time; the caregiving situation is not stable (i.e., there must be no scheduled custody hearings); English is not the primary language spoken in the home. Additionally, caregivers with a psychiatric hospitalization in the past year will be ineligible to participate. Children with certain types of metal in their heads will be unable to participate in the MRI portion but will be able to participate in the intervention and complete pre- and post-intervention questionnaires.

Design outcomes

Primary

MeasureTime frameDescription
Satisfaction SurveyWeek 10Satisfaction with Intervention
Center for Epidemiologic Studies Depression Scale (CES-D)Week 1Caregiver Depression; Scores range from 0 to 60, with high scores indicating greater depressive symptoms.
Adverse Childhood Experiences Scales (ACES)Week 1Caregiver Stress; Scores range from 0 to 10, with higher scores indicating a higher risks for developing later health problems.
Pediatric Quality of Life Inventory (PedsQL)Week 1Child functioning and quality of life
Dyadic Parent Child Interaction Coding System (DPICS)Week 1Parenting Behaviors
Eyberg Child Behavior Inventory (ECBI)Week 1Child Behavior
Child Behavior ChecklistWeek 1Child Behavior
Behavior Rating Inventory of Executive Functions-2Week 1Executive Function Behaviors

Secondary

MeasureTime frameDescription
3D-T1 weighted sequencesWeek 1Neuroimaging-MRI/DTI
3D T2- weighted sequenceWeek 1Neuroimaging-MRI/DTI
Resting state fMRI sequenceWeek 1Neuroimaging-MRI/DTI
Multi-shell diffusion sequenceWeek 1Neuroimaging-MRI/DTI

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026