Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2026-03-26 @ 3:17 PM
Ignite Modification Date: 2026-03-26 @ 3:17 PM
NCT ID: NCT07385469
Eligibility Criteria: Inclusion Criteria: * Inclusion Criteria (for the child): * Having been diagnosed with ARFID according to the DSM-5 by a Child and Adolescent Mental Health and Diseases psychiatrist (Assoc. Prof. Dr. Hakan ÖĞÜTLÜ). * Being between the ages of 3 and 8. * Being medically stable for outpatient treatment. * Having no conditions (visual, auditory, cognitive, or chewing) that would prevent participation in treatment. Inclusion Criteria (for the mother): * Being the child's primary caregiver and living with the mother. * Having at least a primary school diploma and possessing Turkish reading and comprehension proficiency. * Agreeing to take an active role in the intervention process and participate in research evaluations. * Being a regular participant in the child's feeding process. * Not having another child with special needs. Exclusion Criteria: * Exclusion Criteria (Child): * History of comorbid neurological, genetic, psychiatric, or metabolic disease * Child and family receiving other individual or family-based education and/or psychotherapy during the intervention * Taking medication for comorbid disorders affecting appetite and/or weight * Active psychiatric crisis (e.g., severe anxiety disorder, post-traumatic stress disorder) * Significant family or environmental constraints that would prevent regular attendance Exclusion Criteria (Mother): * Severe hearing, vision, or cognitive impairment * Child concurrent participation in another intervention program (dietician, psychotherapy, group education, etc.) related to feeding behaviors * Presence of a chronic health condition (e.g., neurological, psychiatric, orthopedic, oncological, etc.) that would prevent regular attendance at the intervention
Healthy Volunteers: False
Sex: ALL
Minimum Age: 3 Years
Maximum Age: 8 Years
Study: NCT07385469
Study Brief:
Protocol Section: NCT07385469