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Trial Title:
Feasibility and Acceptability of Internet-based Parent-child Interaction Therapy (I-PCIT) in Pediatric Cancer
NCT ID:
NCT06346782
Condition:
Pediatric Cancer
Oncology
Disruptive Behavior
Conditions: Official terms:
Problem Behavior
Conditions: Keywords:
Pediatric Cancer
Oncology
Parent
Parenting
Disruptive Behavior
Study type:
Interventional
Study phase:
N/A
Overall status:
Recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Intervention model description:
This is a pilot feasibility trial. We are using a 2:1 (intervention: waitlist control)
randomized controlled design.
Primary purpose:
Supportive Care
Masking:
None (Open Label)
Intervention:
Intervention type:
Behavioral
Intervention name:
Internet-Based Parent-Child Interaction Therapy
Description:
I-PCIT consists of two phases. The first phase is designed to enhance positive
parent-child interactions. The second phase is designed to enhance parents' behavior
management parenting behaviors.
Arm group label:
I-PCIT
Arm group label:
Waitlist Control
Other name:
I-PCIT
Summary:
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.
Detailed description:
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, the investigators will randomly assign the
participants 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.
I-PCIT is language-dependent. The investigators will make every effort to recruit a
Spanish-speaking fellow clinician for this study. However, if unable to recruit a
Spanish-speaking fellow, a licensed clinical social worker and certified Spanish
interpreter, will provide I-PCIT services to Spanish-speaking families. Children may
participate even if the child cannot produce spoken language. Participants may request
that research personnel read all assessment materials aloud in a structured interview
format, in which case participants could provide verbal item responses. Because of this
option, participants' ability to read and write are not requirements for participation.
The I-PCIT intervention will consist of 13 weekly telehealth sessions with a clinician
who is certified in PCIT. The first telehealth session will take about 60-75 minutes. The
rest of the telehealth sessions will take about 40-60 minutes. I-PCIT teaches parents how
to build more positive interactions with the child and how to improve management of the
child's behavior challenges.
Parents who receive I-PCIT in this study will not be charged for any I-PCIT services.
Parents who are assigned to the waitlist until I-PCIT begins and may continue receiving
any other services to help manage the child's behavior while waiting to start I-PCIT.
The study will last about 5-5 ½ months for parents who are assigned to start I-PCIT right
away. For parents who are assigned to the waitlist to start I-PCIT in 5-6 months, parents
will complete the study, including I-PCIT sessions, in about 8-9 months.
In addition to the initial survey to see if parents are eligible for I-PCIT, parents who
are assigned to I-PCIT or the waitlist will also be asked to complete follow-up surveys
3-4 times during the study.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Participants will be parents of 2-12 year-old children who (1) currently or
previously received cancer treatment and/or long-term cancer follow-up care at Johns
Hopkins All Children's Hospital (JHACH).
- The child's cancer treatment must have included or plan to include chemotherapy
and/or radiation.
- The child's cancer diagnosis must have been conferred at least 6 weeks prior to
study enrollment. If a patient's cancer relapses during the study period, the
patient's oncologist must agree to the patient continuing in this intervention.
- The parent must have access to reliable internet service (e.g., in their own home,
in a friend or family member's home, via cell phone carrier) and their own
smartphone, tablet, or computer to participate in telehealth intervention sessions.
Exclusion Criteria:
- Parents will be excluded if they or their child have cognitive, motor, or language
delays that would preclude participation, as observed by research staff or listed in
the child's medical record. Hearing impaired parents will also be excluded because
I-PCIT requires the coach to verbally coach parents via bug-in-ear.
- Parents will be excluded if their child is expected to undergo bone marrow
transplant (BMT) during the study or has received BMT within 2 months of study
enrollment.
- The child must not be receiving end of life care, as determined by medical chart
review and/or consultation with the patient's medical team.
Gender:
All
Minimum age:
N/A
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Johns Hopkins All Children's Hospital
Address:
City:
Saint Petersburg
Zip:
33701
Country:
United States
Status:
Recruiting
Contact:
Last name:
Melissa Faith, Ph.D.
Phone:
727-295-8477
Email:
mfaith1@jhmi.edu
Start date:
February 19, 2024
Completion date:
August 1, 2028
Lead sponsor:
Agency:
Johns Hopkins All Children's Hospital
Agency class:
Other
Source:
Johns Hopkins All Children's Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06346782