UnknownNot Applicable

A Two-Session Exposure Treatment and Parent Training for ARFID

United States40 participantsStarted 2021-02-15

Plain-language summary

This study aims to assess the acceptability, feasibility, and preliminary efficacy of a two-session, virtual parent-training exposure protocol for children ages 5-12 who experience picky eating consistent with an Avoidant-Restrictive Food Intake Disorder (ARFID) diagnosis.

Who can participate

Age range5 Years – 12 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Children ages 5-12 * Child meets criteria for ARFID using the Pica, ARFID, Rumination Disorder Interview * Established care with a primary care provider * Not engaging in other medication or psychotherapy for ARFID during this treatment trial * Fluently speak and read English Exclusion Criteria: * Child or parent experiencing suicidal thoughts * Child or parent experiencing psychotic symptoms * Child has a cognitive functioning disability

What they're measuring

Recruitment Feasibility

Timeframe: Enrollment

Retention Feasibility

Timeframe: Through study completion, up to 9 months

Acceptability of exposure protocol

Timeframe: Through study completion, up to 9 months

Credibility of treatment

Timeframe: After week 2 of treatment

Acceptability of treatment

Timeframe: After week 2 of treatment

Acceptability of treatment at 1-month follow-up

Timeframe: 1 month

Trial details

NCT IDNCT04913194

SponsorUniversity at Albany

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-12-31

Contact for this trial

Courtney E Breiner, MA

518-376-2543 cbreiner@albany.edu

View on ClinicalTrials.gov More Avoidant Restrictive Food Intake Disorder trials