NCT06630000 Focused Acceptance and Commitment Therapy (FACT)
| NCT ID | NCT06630000 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Children's Mercy Hospital Kansas City |
| Condition | Pediatric Feeding Disorders |
| Study Type | INTERVENTIONAL |
| Enrollment | 80 participants |
| Start Date | 2024-10-14 |
| Primary Completion | 2027-01-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 80 participants in total. It began in 2024-10-14 with a primary completion date of 2027-01-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This is a randomized clinical trial of Focused Acceptance and Commitment Therapy (FACT) vs. an attention-control condition (placebo) for improving the mental health of parents of children with pediatric feeding disorder. The goal of this clinical trial is to compare two programs in parents of children with pediatric feeding disorders. The main question\[s\] it aims to answer are: FACT will result in clinically meaningful reductions in Mental Health(MH) problems among parents of children with Pediatric Feed Disorder (PFD) Identify factors that impact the feasibility of FACT delivery Participants will asked to participate in one of two programs focused on parents of children with pediatric feeding disorders. The participants will also be asked to complete a battery of questionnaires at four timepoints during the study. The parents will be asked to video record a meal time three times during study. Researchers will compare the FACT group with a control group to see if FACT will result in clinically meaningful change in parent stress and anxiety, and parent use of positive mealtime behaviors.
Eligibility Criteria
Inclusion Criteria: * 1\) Must be a parent aged 18+ (primary caregiver) of 2-6-year-old child with PFD * 2\) Child must be receiving outpatient PFD treatment at CMH * 3\) The parent must have a clinically significant elevation on at least one measure of parent MH (using established clinical cutoffs). Parents will be included regardless of whether the child has a new diagnosis or established diagnoses Exclusion Criteria: * 1\) Parent has significant cognitive impairments * 2\) Parent does not speak English * 3\) Parent unable to obtain high speed internet at home
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06630000 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Pediatric Feeding Disorders. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06630000 currently recruiting?
Yes, NCT06630000 is actively recruiting participants. Contact the research team at crschurman@cmh.edu for enrollment information.
Where is the NCT06630000 trial being conducted?
This trial is being conducted at Kansas City, United States.
Who is sponsoring the NCT06630000 clinical trial?
NCT06630000 is sponsored by Children's Mercy Hospital Kansas City. The trial plans to enroll 80 participants.