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Longitudinal, Multi-Dimensional Assessment of Recovery and Added Benefit of a Behavioral Health Intervention for Children With Abusive Head Trauma

University of Colorado Denver (CU Denver) logo

University of Colorado Denver (CU Denver)

Status

Completed

Conditions

Non-Accidental Traumatic Head Injury to Child

Treatments

Behavioral: Attachment and Biobehavioral Catch-up (ABC)

Study type

Interventional

Funder types

Other

Identifiers

NCT03447899
IHEA101376 (Other Grant/Funding Number)
17-1221

Details and patient eligibility

About

Family dynamics and caregiver responses to a child with traumatic brain injury are implicated both as precipitating events as well as factors influencing outcomes of abusive head trauma (AHT). However, no family behavioral health intervention exists to meet the unique needs of families with infants and very young children with AHT. The study was initially designed as a randomized controlled trial (RCT) to assess the efficacy of an evidence-based behavioral intervention to improve outcomes for families and children with AHT. However, rates of recruitment were so low that the investigators and funder amended the study to be intervention only (with IRB approval). At that time, there were five participants and only one had been assigned to the intervention arm. Only one additional family was recruited, and that family did not complete study measures prior to the time at which the intervention would start and did not receive the intervention. The investigators did examine outcomes in multiple dimensions, including clinical, cognitive, family, caregiver, child behavior, and service usage over time but connot compare to patients not receiving the intervention. The investigators were not able to examine characteristics of patients and families best suited for this behavioral health intervention.

Full description

27 children (ages 3 months to 2 years) and their caregiver referred to the Non-Accidental Brain Injury Care Clinic at the Children's Hospital Colorado (CHCO) were recruited for participation in the study, 7 families consented. One family received the Attachment and Biobehavioral (ABC) intervention. One family discontinued participation. The data collection schedule was 1 month post-injury, 3 months, 6 months, 9 months, and 12 months. Outcomes in multiple dimensions, were assessed including clinical recovery, cognitive, language, and motor functioning, family functioning, caregiver mental health including anxiety, depression, competency, and stress. The investigators also examined service use over time. Analyses will assess trajectories of recovery for both groups using data for all time points.

Enrollment

7 patients

Sex

All

Ages

3 months to 2 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children who have experienced AHT as determined by the CHCO Child Protection Team
  • Caregivers who speak English
  • Families who live in the Denver Metro area and,
  • Child-victim age between 3 months and 2 years of age

Exclusion criteria

  • Those with significant disability that would inhibit participation in the intervention,
  • Those scoring below 6 months on developmental measures will not be eligible.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

7 participants in 2 patient groups

ABC Intervention
Experimental group
Description:
The investigators will deliver the "Attachment and Biobehavioral Catch-up (ABC)" in the home weekly using live, in-room coaching, to give caregivers feedback as they use targeted skills during interactions with the child. The intervention will last 10 sessions. Study participants in both groups will complete study measures at baseline, 1 month, 3 months, post-intervention, 6 months, and 12 months.
Treatment:
Behavioral: Attachment and Biobehavioral Catch-up (ABC)
Standard of Care
No Intervention group
Description:
Subjects will receive normal standard of care without the "Attachment and Biobehavioral Catch-up (ABC)".

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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