SOS OPC ARFIDSOS Feeding Approach and Occupational Performance Coaching for Children with ARFID
This study aims to evaluate the effectiveness of the SOS Feeding Approach and Occupational Performance Coaching in improving feeding behaviors and sensory processing abilities in children with Avoidant/Restrictive Food Intake Disorder (ARFID).
Sequential Oral Sensory (SOS) Feeding Approach
+ SOS + Occupational Performance Coaching (OPC)
Avoidant Restrictive Food Intake Disorder+3
+ Feeding and Eating Disorders
+ Mental Disorders
Supportive Care Study
Summary
Study start date: January 15, 2026
Actual date on which the first participant was enrolled.This study focuses on Avoidant/Restrictive Food Intake Disorder (ARFID), a serious condition related to feeding behavior. ARFID is characterized by significant weight loss, marked nutritional deficiencies, dependence on feeding tubes or supplements, and impaired psychosocial functioning. It affects approximately 3.2% of the general pediatric population and is often associated with comorbid psychiatric and/or medical conditions. This study seeks to address the lack of sensory- and behaviorally-oriented feeding interventions for ARFID by evaluating the effects of the Sequential Oral Sensory (SOS) Feeding Approach and Occupational Performance Coaching (OPC) on feeding problems and behaviors of children with ARFID, as well as on parental feeding attitudes and mealtime behaviors. The Sequential Oral Sensory (SOS) Feeding Approach is a structured intervention that supports sensory-motor skills related to feeding and aims to develop a positive relationship with food. By gradually increasing interaction with food, the SOS approach aims to reduce sensory sensitivities and improve feeding behaviors. Occupational Performance Coaching (OPC) is a structured, problem-solving, guidance, and empowerment-based approach designed to help parents support their children's daily life performance. This randomized controlled single-blind study will measure the effects of these interventions using the Behavioral Pediatric Feeding Scale, Children's Eating Behaviour Questionnaire, Goal Attainment Scaling (GAS), Sensory Eating Problems Scale, and Sensory Profile. The study aims to make an original contribution to the development of applicable and effective intervention models for children and families dealing with ARFID.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.45 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 3 to 8 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
Active ComparatorGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Hacettepe University, Department of Occupational Therapy, Pediatric Unit
Ankara, Turkey (Türkiye)Open Hacettepe University, Department of Occupational Therapy, Pediatric Unit in Google Maps