Actively Recruiting
Feasibility and Acceptability of Internet-based Parent-child Interaction Therapy (I-PCIT) in Pediatric Cancer
Led by Johns Hopkins All Children's Hospital · Updated on 2026-04-30
300
Participants Needed
1
Research Sites
232 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is being done to learn whether a telehealth intervention called "Internet-Based Parent Child Interaction Therapy," or I-PCIT," can help parents improve the child's behavior if the child currently or previously went through cancer treatment. Parents who choose to be in this study will complete a survey to help researchers figure out if the parent is eligible for the larger study. If a parent is eligible for the larger study and chooses to participate, if so, the participants will be randomly assigned to either receive the I-PCIT intervention now or to be on a waitlist and begin I-PCIT in 5-6 months. The whole study consists of completing I-PCIT sessions with a clinician and completing 3-4 follow-up surveys after the initial screener survey.
CONDITIONS
Official Title
Feasibility and Acceptability of Internet-based Parent-child Interaction Therapy (I-PCIT) in Pediatric Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Parents of children aged 2 to 12 years who currently or previously received cancer treatment or long-term follow-up at Johns Hopkins All Children's Hospital
- Child's cancer treatment included or will include chemotherapy and/or radiation
- Child's cancer diagnosis was made at least 6 weeks before enrolling in the study
- If the child's cancer relapses during the study, the oncologist must approve continued participation
- Parent has reliable internet access and owns a smartphone, tablet, or computer for telehealth sessions
You will not qualify if you...
- Parent or child has cognitive, motor, or language delays that prevent participation as noted by staff or medical records
- Parent is hearing impaired since verbal coaching via bug-in-ear is required
- Child is expected to undergo bone marrow transplant during the study or had one within 2 months before enrolling
- Child is receiving end of life care as determined by medical review or medical team consultation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Johns Hopkins All Children's Hospital
St. Petersburg, Florida, United States, 33701
Actively Recruiting
Research Team
M
Melissa Faith, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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