Actively Recruiting

Phase Not Applicable
Age: 12Years - 25Years
All Genders
Healthy Volunteers
NCT06463470

Cognitive Behavioural Therapy for Avoidant/Restrictive Food Intake Disorder (CBT-AR)

Led by Orygen · Updated on 2025-07-11

20

Participants Needed

2

Research Sites

156 weeks

Total Duration

On this page

Sponsors

O

Orygen

Lead Sponsor

U

University of Melbourne

Collaborating Sponsor

AI-Summary

What this Trial Is About

CBT-AR describes an adaption of cognitive behavioural therapy for use with individuals diagnosed with Avoidant/Restrictive Food Intake Disorder (ARFID). The purpose of this evaluation is to determine the feasibility, acceptability and effectiveness of this treatment. It is hypothesised that this treatment will be feasible and acceptable to clinicians, carers and patients and will be effective in reducing symptoms of ARFID for patients.

CONDITIONS

Official Title

Cognitive Behavioural Therapy for Avoidant/Restrictive Food Intake Disorder (CBT-AR)

Who Can Participate

Age: 12Years - 25Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Current primary diagnosis of Avoidant/Restrictive Food Intake Disorder (ARFID) according to DSM-5 criteria as determined by the treating team
  • Presenting for treatment in the eating disorders Orygen Specialist Program
  • If under 16 years old, or over 16 but underweight (BMI less than 18.5) and living with parents or guardian, a parent or guardian must be involved in treatment
Not Eligible

You will not qualify if you...

  • Current tube feeding
  • Inappropriateness for CBT-AR as determined by clinicians, such as urgent issues like high suicidal ideation or inadequate comprehension capability

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 2 locations

1

Orygen Youth Health - Sunshine - Sunshine

Melbourne, Victoria, Australia, 3020

Actively Recruiting

2

Orygen Youth Health - Parkville - Parkville

Melbourne, Victoria, Australia, 3052

Actively Recruiting

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Research Team

A

Andrea Phillipou

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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