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. Author manuscript; available in PMC: 2024 Mar 1.
Published in final edited form as: Int J Eat Disord. 2022 Dec 22;56(3):616–627. doi: 10.1002/eat.23874

Table 1.

Overview of Quantitative Measures.

Primary Outcomes Part 1 Study Part 2 Study Pre-treatment sample size Mid-treatment sample sizea Post-treatment sample sizeb
Primary Outcomes
NIAS X X 14 10 11
PAGI-SYM c X X 13 8 11
VSI X X 14 9 11
Weight X X 10 10 9
Secondary Outcomes
PARDI-ARQ X 5 5 4
SF-NDI Quality of Life X 5 5 4
PAGI-QOL X 5 5 4
Fear of Food Questionnaire X 5 5 4
Food Neophobia Scale X 5 5 4

Note.NIAS=Nine Item AFRID Screen; PAGI-SYM=Patient Assessment of Gastrointestinal Disorders Symptom Severity Index; VSI=Visceral Sensitivity Index; ARFID=Avoidant/Restrictive Food Intake Disorder; GI=gastrointestinal; PARDI=Pica, ARFID, and Rumination Disorder Interview; SF-NDI=Short Form Nepean Dyspepsia Index; PAGI-QOL=Patient Assessment of Upper Gastrointestinal Disorders Quality of Life.

a

Missing mid-treatment data for the NIAS, PAGI-SYM, and VSI if they were not administered at mid-treatment in clinical care (in Part 1 retrospective study).

b

Missing data for n=1 because the participant dropped out of treatment at Session 4 (in Part 2 observational prospective study) and n=2 participants because the NIAS, PAGI-SYM, and VSI were not administered in clinical care (in Part 1 retrospective study).

c

Missing data n=1 participant because the PAGI-SYM was not administered in clinical care (in Part 1 retrospective study).