Cognitive-behavioral therapy for adults with avoidant/restrictive food intake disorder
Open accessAbstract
There are currently no evidence-based treatments for adults with avoidant/restrictive food intake disorder (ARFID). The purpose of this study was to evaluate the acceptability, feasibility, and proof-of-concept of cognitive-behavioral therapy for ARFID (CBT-AR) for adults. Males and females (ages 18–55 years) were offered 20-30 outpatient sessions of CBT-AR delivered by one of five therapists. Of 18 eligible adults offered CBT-AR, 15 chose to participate and 14 completed treatment. All patients endorsed high ratings of treatment credibility and expected improvement after the first session, and 93% of completers provided high ratings of satisfaction at the conclusion of treatment. Therapists rated the majority (80%) of patients as “much improved” or “very much improved.” Based on intent-to-treat analyses, ARFID severity on the Pica, ARFID, and Rumination Disorder Interview (PARDI) showed a large and significant decrease from pre- to post-treatment; and patients incorporated a mean of 18.0 novel foods. The underweight subgroup (n = 4) gained an average of 11.38 pounds, showing a large and significant increase in mean BMI from the underweight to the normal-weight range. At post-treatment, 47% of patients no longer met criteria for ARFID. To our knowledge, this is the first prospective treatment study of ARFID in adults. The findings of this study provide preliminary evidence of feasibility, acceptability, and proof-of-concept of CBT-AR for heterogeneous presentations of ARFID in adults. Randomized controlled trials are needed to confirm these findings. ClinicalTrials.gov Identifier: NCT02963220.
AI snapshot
Written from the paper’s full text.
TL;DR
This first prospective treatment study of adults with avoidant/restrictive food intake disorder (ARFID) found that cognitive-behavioral therapy for ARFID (CBT-AR) was feasible, acceptable, and showed preliminary proof-of-concept. Of 15 adults who initiated treatment, 14 completed, with significant reductions in ARFID severity and 47% no longer meeting ARFID criteria at post-treatment.
Key findings
- Of 18 eligible adults offered CBT-AR, 15 chose to participate and 14 completed treatment; 93% of completers rated high satisfaction on the CSQ.
- Therapists rated 80% of patients as “much improved” or “very much improved” on the CGI.
- Intent-to-treat analyses showed a large and significant decrease in PARDI ARFID overall severity (p < .001); patients incorporated a mean of 18.0 (SD = 13.2) novel foods.
- The underweight subgroup (n = 4) gained an average of 11.38 (SD = 7.47) pounds, with a significant increase in mean BMI (p = .04) and all four achieving BMI > 18.5; 47% (n = 7) no longer met ARFID criteria at post-treatment (p = .01). Anxiety (p = .78) and depression (p = .26) did not change.
Methods
- Open pilot/proof-of-concept study of adults ages 18–55 years recruited from an observational neurobiology study (ages 18–23) and consecutive clinical referrals for ARFID treatment at Massachusetts General Hospital.
- Patients received 20–30 outpatient CBT-AR sessions delivered by one of five doctoral or master’s level therapists; treatment was manualized, with high fidelity (M = 6.96, SD = 0.21 on a 7-point scale) and competence (M = 4.99, SD = 0.11 on a 5-point scale).
- Intent-to-treat analyses used paired t-tests, McNemar’s chi squared tests, and Cohen’s d; post-treatment assessments were conducted on all patients except one dropout, for whom baseline assessment was carried forward.
Limitations
- The authors state the sample size was small, effect size estimates may be unstable, and p-values require cautious interpretation.
- The authors state there was no control group, so alternative explanations such as therapist attention or passage of time cannot be ruled out.
- The authors also state possible recruitment/payment effects on low dropout, a mostly non-Hispanic white sample, use of the KSADS with a subset of young adults, and limited ability to draw conclusions about family-supported CBT-AR for adults.
Model-written summary. Check it against the paper before relying on it.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
0 of 25 cited sources checked · 0 supported · 0 flagged
- Findingown data
All patients endorsed high ratings of treatment credibility and expected improvement after the first session.
“All patients endorsed high ratings of treatment credibility and expected improvement after the first session”
Quote in the paperSubstantial claim - Findingown data
Of 18 eligible adults offered CBT-AR, 15 chose to participate.
“Of the 18 patients offered CBT-AR, 15 chose to participate.”
Quote in the paperSubstantial claim - Findingown data
PARDI fear of aversive consequences decreased at trend level (p = .06) with a small effect size.
“PARDI fear of aversive consequences decreased at trend level with a small effect size (p = .06).”
Quote in the paperNot a substantial claim - Findingown data
The underweight subgroup (n = 4) gained an average of 11.38 (SD = 7.47) pounds.
“The underweight subgroup (n = 4) gained an average of 11.38 (SD = 7.47) pounds”
Quote in the paperSubstantial claim - Findingown data
Approximately half of the sample received some or all CBT-AR sessions via video.
“Approximately half of our sample received some or all CBT-AR sessions via video.”
Quote in the paperNot a substantial claim
- Findingown data
Anxiety did not change significantly (p = .78).
“though anxiety (p = .78) and depression (p = .26) did not change.”
Quote in the paperNot a substantial claim - Findingown data
93% of completers provided high ratings of satisfaction at the conclusion of treatment.
“93% of completers provided high ratings of satisfaction at the conclusion of treatment.”
Quote in the paperSubstantial claim - Findingown data
All four underweight patients achieved a BMI > 18.5 at post-treatment.
“All four patients who were underweight at pre-treatment achieved a BMI > 18.5 at post-treatment.”
Quote in the paperSubstantial claim - Findingown data
PARDI lack of interest decreased significantly (p = .03) with a small effect size.
“PARDI lack of interest decreased significantly (p = .03) with a small effect size”
Quote in the paperNot a substantial claim - Findingown data
Depression did not change significantly (p = .26).
“though anxiety (p = .78) and depression (p = .26) did not change.”
Quote in the paperNot a substantial claim - Findingown data
Therapists rated 80% of patients as "much improved" or "very much improved" on the CGI.
“Therapists rated 80% of patients as “much improved” or “very much improved” on the CGI.”
Quote in the paperSubstantial claim - Findingown data
ARFID overall severity on the PARDI decreased significantly from pre- to post-treatment with a large effect size.
“patient PARDI ratings of ARFID overall severity (p < .001) and sensory sensitivity (p < .001) decreased significantly with large effect sizes.”
Quote in the paperSubstantial claim - Findingown data
PARDI sensory sensitivity decreased significantly from pre- to post-treatment with a large effect size.
“patient PARDI ratings of ARFID overall severity (p < .001) and sensory sensitivity (p < .001) decreased significantly with large effect sizes.”
Quote in the paperSubstantial claim - Findingown data
Food neophobia decreased significantly (p < .001) with a large effect size.
“Food neophobia decreased significantly (p < .001) with a large effect size.”
Quote in the paperSubstantial claim - Findingown data
Patients incorporated a mean of 18.0 (SD = 13.2) new foods from pre- to post-treatment.
“Patients incorporated a mean of 18.0 (SD = 13.2) new foods from pre- to post-treatment, primarily from groups underrepresented in their diets including fruits, vegetables, and proteins.”
Quote in the paperSubstantial claim - Findingown data
14 patients completed treatment.
“Fourteen patients completed treatment.”
Quote in the paperSubstantial claim - Findingown data
Clinical impairment decreased significantly (p = .02) with a medium effect size.
“Clinical impairment also decreased significantly (p = .02) with a medium effect size”
Quote in the paperSubstantial claim- Rests on an assumption: The Clinical Impairment Assessment (CIA) measures functional impairment related to eating, shape, and weight in adults with eating disorders.
- Premisecitation
There are currently no evidence-based treatments for adults with avoidant/restrictive food intake disorder (ARFID).
“There are currently no evidence-based treatments for adults with avoidant/restrictive food intake disorder (ARFID).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Dalle Grave & Sapuppo, 2020
Not checked in the free run.
- Premisecitation
In a prior study of CBT-AR in children and adolescents, patients added an average of 16.7 novel foods.
“In that study, the majority of patients (85%) completed treatment, and completers reported high levels of treatment satisfaction. Furthermore, patients demonstrated significant decreases in ARFID severity from pre- to post-treatment, added an average of 16.7 novel foods to their diet, and—at the conclusion of treatment—70% no longer met criteria for ARFID (Thomas et al., 2020).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Thomas et al., 2020 source
Not checked in the free run.
- Premisecitation
A handful of recent case reports have highlighted the potential of cognitive-behavioral therapy (CBT) for adults with ARFID.
“A handful of recent case reports have highlighted the potential of cognitive-behavioral therapy (CBT) for adults (e.g., Aloi, Sinopoli, & Segura-Garcia, 2018; Görmez, Kılıç, & Kırpınar, 2018; Steen & Wade, 2018).”
Quote in the paperSubstantial claim0 of 3 sources checked - Premisecitation
No published studies have evaluated the efficacy of any intervention for ARFID in adults.
“However, no published studies have evaluated the efficacy of any intervention for ARFID in adults (for review, see Dalle Grave & Sapuppo, 2020).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Dalle Grave & Sapuppo, 2020
Not checked in the free run.
- Rests on an assumption: The majority of research on ARFID has focused on children.
- Premisecitation
In a prior study of CBT-AR in children and adolescents, completers reported high levels of treatment satisfaction.
“In that study, the majority of patients (85%) completed treatment, and completers reported high levels of treatment satisfaction. Furthermore, patients demonstrated significant decreases in ARFID severity from pre- to post-treatment, added an average of 16.7 novel foods to their diet, and—at the conclusion of treatment—70% no longer met criteria for ARFID (Thomas et al., 2020).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Thomas et al., 2020 source
Not checked in the free run.
- Interpretationown data
The spread of COVID-19 mid-way through the trial enabled observations about the potential feasibility of conducting CBT-AR via telehealth.
“The spread of COVID-19 mid-way through the trial enabled us to make observations about the potential feasibility of conducting CBT-AR via telehealth.”
Quote in the paperSubstantial claim - Study design and conductown data
Treatment fidelity was high (M = 6.96, SD = 0.21 on a 7-point scale).
“Ratings of two randomly selected sessions for each of 15 patients indicated high levels of fidelity (M = 6.96, SD = 0.21, on a 7-point scale) and competence (M = 4.99, SD = 0.11, on a 5-point scale).”
Quote in the paperNot a substantial claim - Study design and conductown data
There is limited ability to draw conclusions about proof-of-concept for family-supported CBT-AR for adults given most patients received the individual version.
“Lastly, we have limited ability to draw conclusions about proof-of-concept for family-supported CBT-AR for adults given that most patients received the individual version.”
Quote in the paperSubstantial claim - Premisecitation
There are promising psychosocial treatments for ARFID in children and adolescents.
“There are currently a number of promising psychosocial treatments for ARFID in children and adolescents (e.g., Dumont, Jansen, Kroes, de Haan, & Mulkens, 2019); Lock, Sadeh-Sharvit, & L’Insalata, 2019; Sharp et al., 2016; Thomas et al., in press).”
Quote in the paperNot a substantial claim0 of 3 sources checked - Premisecitation
In a prior study of CBT-AR in children and adolescents, patients demonstrated significant decreases in ARFID severity from pre- to post-treatment.
“In that study, the majority of patients (85%) completed treatment, and completers reported high levels of treatment satisfaction. Furthermore, patients demonstrated significant decreases in ARFID severity from pre- to post-treatment, added an average of 16.7 novel foods to their diet, and—at the conclusion of treatment—70% no longer met criteria for ARFID (Thomas et al., 2020).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Thomas et al., 2020 source
Not checked in the free run.
- Study design and conductown data
Inter-rater reliability for comorbid diagnoses for 20% randomly selected cases was 100% (kappa = 1.0).
“Inter-rater reliability for 20% of randomly selected cases (including two KSADS and one MINI) was 100% (kappa = 1.0) for comorbid diagnoses.”
Quote in the paperNot a substantial claim - Premisecitation
In a prior study of CBT-AR in children and adolescents (ages 10-17), 85% completed treatment.
“In that study, the majority of patients (85%) completed treatment, and completers reported high levels of treatment satisfaction. Furthermore, patients demonstrated significant decreases in ARFID severity from pre- to post-treatment, added an average of 16.7 novel foods to their diet, and—at the conclusion of treatment—70% no longer met criteria for ARFID (Thomas et al., 2020).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Thomas et al., 2020 source
Not checked in the free run.
- Interpretationcitation
Findings are consistent with positive outcomes of single case reports of CBT for ARFID in adults.
“Our findings are consistent with positive outcomes of single case reports of CBT for ARFID in adults (e.g., Aloi et al., 2018; Görmez et al., 2018; Steen & Wade, 2018)”
Quote in the paperNot a substantial claim0 of 3 sources checked - Interpretationcitation
The post-treatment remission rate of 47% was somewhat lower than the 70% reported for children and adolescents in a previous trial.
“Although adults in this study made significant improvements with CBT-AR, the post-treatment remission rate of 47% was somewhat lower than the 70% we reported for our previous trial of CBT-AR in children and adolescents (Thomas et al., 2020).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Thomas et al., 2020 source
Not checked in the free run.
- Study design and conductown data
Internal consistency for PARDI severity and profile ratings ranged from 0.89 to 1.0 in the current sample.
“Internal consistency (measured via McDonald’s omega to account for skewed data) for the severity and profile ratings ranged from 0.89 to 1.0 in the current sample.”
Quote in the paperNot a substantial claim - Study design and conductown data
Inter-rater reliability of the ARFID diagnosis for 20% randomly selected cases at both pre- and post-treatment was excellent (100% agreement; kappa = 1.0).
“Inter-rater reliability of the ARFID diagnosis (yes/no) for 20% of randomly selected cases at both pre- and post-treatment was excellent (100% agreement; kappa = 1.0).”
Quote in the paperNot a substantial claim - Premisecitation
In a prior study of CBT-AR in children and adolescents, 70% no longer met criteria for ARFID at conclusion.
“In that study, the majority of patients (85%) completed treatment, and completers reported high levels of treatment satisfaction. Furthermore, patients demonstrated significant decreases in ARFID severity from pre- to post-treatment, added an average of 16.7 novel foods to their diet, and—at the conclusion of treatment—70% no longer met criteria for ARFID (Thomas et al., 2020).”
Quote in the paperSubstantial claim0 of 1 sources checked- cites Thomas et al., 2020 source
Not checked in the free run.
- Interpretationnone given
This is the first prospective treatment study of ARFID in adults.
“To our knowledge, this is the first prospective treatment study of ARFID in adults.”
Quote in the paperNot a substantial claim - Study design and conductown data
Therapist competence was high (M = 4.99, SD = 0.11 on a 5-point scale).
“Ratings of two randomly selected sessions for each of 15 patients indicated high levels of fidelity (M = 6.96, SD = 0.21, on a 7-point scale) and competence (M = 4.99, SD = 0.11, on a 5-point scale).”
Quote in the paperNot a substantial claim - Study design and conductreasoning
With no control group, alternative rival hypotheses for the observed improvements cannot be ruled out.
“Second, with no control group we cannot rule out alternative rival hypotheses for the observed improvements (e.g., therapist attention, passage of time).”
Quote in the paperSubstantial claim
- May combine two claims. 11
- Classified as probably not a substantial claim. 12
May combine two claims.
Findingown dataThe underweight subgroup showed a trend-level increase in weight (p = .06) with a large effect size.
“representing a trend-level increase in weight (p = .06) and a significant increase in BMI (p = .04), both with large effect sizes.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
Findingown dataOne patient dropped out after two sessions.
“One patient dropped out after two sessions in the setting of flu-like and gastrointestinal symptoms.”
Quote in the paperNot a substantial claimMay combine two claims.
Findingown data47% (n = 7) of patients no longer met criteria for ARFID at post-treatment, a significant change from pre-treatment when 100% met criteria (p = .01).
“Using the PARDI diagnostic algorithm, 47% (n = 7) of patients no longer met criteria for ARFID at post-treatment, representing a significant change from pre-treatment when 100% met criteria (p = .01).”
Quote in the paperSubstantial claimMay combine two claims.
Findingown dataThe underweight subgroup showed a significant increase in BMI (p = .04) with a large effect size, moving from the underweight to the normal-weight range.
“moving from an average BMI in the underweight range to an average BMI in the normal-weight range, representing a trend-level increase in weight (p = .06) and a significant increase in BMI (p = .04), both with large effect sizes.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing). May combine two claims.
PremisecitationIn a 2014 Australian sample of 3005 people ages 15 and older, the point prevalence of ARFID was 0.3%, compared to 0.4% for anorexia nervosa.
“In a recent study of 3005 Australians ages 15 and older, the point prevalence of ARFID in 2014 was 0.3%, compared to 0.4% for anorexia nervosa (Hay et al., 2017).”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Hay et al., 2017
Not checked in the free run.
May combine two claims.
Study design and conductnone givenThe sample size was small, rendering effect size estimates potentially unstable and requiring cautious interpretation of p-values.
“First and most importantly, the sample size was small, rendering effect size estimates potentially unstable and requiring cautious interpretation of p-values.”
Quote in the paperSubstantial claimMay combine two claims.
Interpretationown dataCBT-AR showed preliminary evidence of feasibility, acceptability, and proof-of-concept for adults with ARFID.
“In our initial study of 15 patients, CBT-AR showed preliminary evidence of feasibility, acceptability, and proof-of-concept.”
Quote in the paperSubstantial claim- Rests on an assumption: The Clinical Impairment Assessment (CIA) measures functional impairment related to eating, shape, and weight in adults with eating disorders.
May combine two claims.
Interpretationown dataChildren and adolescents may respond more fully than adults to ARFID treatment, or perhaps have a better overall prognosis.
“The finding that children and adolescents may respond more fully than adults to ARFID treatment, or perhaps have a better overall prognosis, mirrors the literature for anorexia nervosa (e.g., Jagielska & Kacperska, 2017; Kass, Kolko & Wilfley, 2013).”
Quote in the paperSubstantial claim0 of 2 sources checked- cites Jagielska & Kacperska, 2017
Not checked in the free run.
- cites Kass et al., 2013 source
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataThe trial was registered at ClinicalTrials.gov prior to data collection.
“The trial was registered at ClinicalTrials.gov (Identifier: NCT02963220) prior to data collection.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim. May combine two claims.
Study design and conductreasoningSignificance level was set at p < .05 and no correction for family-wise error was made given the preliminary nature of the study.
“We set the significance level at p < .05 and did not correct for family-wise error given the preliminary nature of the study.”
Quote in the paperSubstantial claimClassified as probably not a substantial claim.
Study design and conductown dataIntent-to-treat analyses were used.
“To test our proof-of-concept hypotheses, we considered responses from both therapists and patients using intent-to-treat analyses.”
Quote in the paperSubstantial claimMay combine two claims.
PremisecitationARFID symptoms in adults are severe and impairing.
“The few studies that have examined ARFID and associated psychopathology in adults suggest that its symptoms are severe and impairing (e.g., Nakai, Nin, Noma, Teramukai, & Wonderlich, 2016); Zickgraf, Franklin, & Rozin, 2016)”
Quote in the paperNot a substantial claim0 of 2 sources checkedProbably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductown dataThe KSADS (originally designed for children and adolescents) was used with a subset of young adults.
“Fifth, we used the KSADS (originally designed for use with children and adolescents) with a subset of young adults in the current study who were drawn from a neurobiology study with a younger age range.”
Quote in the paperNot a substantial claimMay combine two claims.
InterpretationcitationVideo delivery had benefits including immediate accessibility of food in the home and increased convenience of attending sessions.
“However, video delivery had many of the benefits previously noted for other forms of behavioral treatment for eating disorders (Matheson et al., 2020; Waller et al., 2020), including the immediate accessibility of food in the home (which facilitated the completion of in-session food preparation and exposures), and the increased convenience of attending sessions (which may have contributed to low”
Quote in the paperSubstantial claim0 of 2 sources checkedClassified as probably not a substantial claim.
Study design and conductnone givenIndependent assessors who were not study therapists conducted all PARDIs.
“Independent assessors who were not study therapists conducted all PARDIs.”
Quote in the paperSubstantial claimProbably not a substantial claim: may not pass S3 (load-bearing).
PremisecitationARFID may be just as common as the better-known eating disorders.
“and that ARFID may be just as common as the better-known eating disorders.”
Quote in the paperNot a substantial claim0 of 1 sources checked- cites Hay et al., 2017
Not checked in the free run.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenRecruiting participants from those already willing to take part in an intensive longitudinal neurobiology study and paying them for completing assessments may have contributed to the low rate of treatment dropout.
“Third, it is possible that recruiting participants from those who were already willing to take part in an intensive longitudinal neurobiology study, and then paying them for completing assessments, may have contributed to the low rate of treatment dropout.”
Quote in the paperNot a substantial claimProbably not a substantial claim: may not pass S2 (checkable).
Interpretationown dataCBT-AR is a promising new treatment worthy of further evaluation for adults with ARFID.
“suggest that CBT-AR is a promising new treatment worthy of further evaluation for adults with ARFID.”
Quote in the paperNot a substantial claimMay combine two claims.
Interpretationown dataFindings suggest that CBT-AR is a potentially efficacious treatment for adults with ARFID that requires more rigorous evaluation.
“Taken together, findings suggest that CBT-AR is a potentially efficacious treatment for adults with ARFID that requires more rigorous evaluation.”
Quote in the paperSubstantial claim- Rests on an assumption: The Clinical Impairment Assessment (CIA) measures functional impairment related to eating, shape, and weight in adults with eating disorders.
Probably not a substantial claim: may not pass S3 (load-bearing).
Study design and conductnone givenMost of the sample was non-Hispanic white.
“Fourth, most of the sample was non-Hispanic white.”
Quote in the paperNot a substantial claimClassified as probably not a substantial claim.
Study design and conductown dataPost-treatment assessments were conducted on all patients except one dropout, for whom baseline assessment was carried forward.
“We conducted post-treatment assessments on all patients, except for our one dropout, for whom we used baseline assessment carried forward.”
Quote in the paperSubstantial claim
The paper relies on this without support.
The majority of research on ARFID has focused on children.
“However, the majority of research has focused on children.”
The paper relies on this without support.
The Clinical Impairment Assessment (CIA) measures functional impairment related to eating, shape, and weight in adults with eating disorders.
“The CIA is a self-report questionnaire that measures functional impairment related to eating, shape, and weight in adults with eating disorders.”
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Preliminary evidence has supported cognitive behavioural therapy for ARFID as an effective treatment for heterogeneous presentations of ARFID in children, adolescents, and adults.
“In particular, preliminary evidence has supported cognitive behavioural therapy for ARFID as an effective treatment for heterogeneous presentations of ARFID in children, adolescents, and adults.[90][91][92]”
From Avoidant/Restrictive Food Intake Disorder and Severe Food Selectivity in Children and Young People with Autism: A Scoping Review (2022) · cites this paper as [92]
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Department of Health Sciences, U. M. G. O. C., Aloi, M., Sinopoli, F., Dietetic Service, U. H. M. D., Segura-Garcia, C., & Department of Health Sciences, U. M. G. O. C. (2108) · Psychiatria Danubina · doi:10.24869/psyd.2018.370 · Cited by 18 · see citing works
Treatment of avoidant/restrictive food intake disorder: a systematic review
Grave, A. D. (2020) · IJEDO · doi:10.32044/ijedo.2020.04 · Cited by 18 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Sheehan, 1998, The Mini International Neuropsychiatric Interview (M.I.N.I.): The development and validation of a structured diagnostic psychiatric interview, Journal of Clinical Psychiatry, 59, 22
Cited by
Sorted by citations
Bourne, L., Mandy, W., & Bryant‐Waugh, R. (2022) · Developmental Medicine & Child Neurology · doi:10.1111/dmcn.15139 · Cited by 110 · see citing works
Eating Problems in Autistic Females and Males: A Co-twin Control Study
Lundin Remnélius, K., Neufeld, J., Isaksson, J., & Bölte, S. (2022) · Journal of Autism and Developmental Disorders · doi:10.1007/s10803-021-05198-z · Cited by 25 · see citing works
Kennedy, H. L., Dinkler, L., Kennedy, M. A., Bulik, C. M., & Jordan, J. (2022) · Journal of Eating Disorders · doi:10.1186/s40337-022-00578-x · Cited by 29 · see citing works
- Authors
- Thomas, J. J., Becker, K. R., Breithaupt, L., Murray, H. B., Jo, J. H., Kuhnle, M. C., Dreier, M. J., Harshman, S., Kahn, D. L., Hauser, K., Slattery, M., Misra, M., Lawson, E. A., & Eddy, K. T.
- Affiliations
- Harvard University (US)
- Massachusetts General Hospital (US)
- Corresponding author
- Thomas, Jennifer J.
- ORCID
- Venue
- Journal of Behavioral and Cognitive Therapy
- Publisher
- Elsevier BV
- Published
- 2021-03
- Volume
- 31
- Issue
- 1
- Pages
- 47-55
- ISSN
- 2589-9791 (ISSN-L)
- PMC
- PMC8375627
- OpenAlex
- W3135691280
- Semantic Scholar
- 9a69a37bf1912771611b54af400743b1fd3e315e
- Cited by
- 88
- References
- 27
- Citations by year
- 2026: 15 · 2025: 18 · 2024: 25 · 2023: 16 · 2022: 11 · 2021: 3
- FWCI
- 9.38
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Behavioral and Cognitive Therapy (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion, cc-by-nc-nd)
- Funders
- Hilda and Preston Davis Foundation
- Massachusetts General Hospital (K24 MH120568, R01 MH108595)
- Global Foundation for Eating Disorders
- National Institute of Mental Health
- American Psychological Foundation
- Topics
- Social Sciences › Psychology › Clinical Psychology › Eating Disorders and Behaviors
- Health Sciences › Medicine › Psychiatry and Mental health › Child Nutrition and Feeding Issues
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
- Keywords
- avoidant/restrictive food intake disorder, cognitive behavioral therapy, adults, treatment acceptability, treatment feasibility, proof of concept, weight gain, underweight, eating disorders
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Claims read by deepseek-v4.1-flash under definition version 3 (extract-v3) on 2026-10-10.
Classified by jev-1.13-20260917 (gold-guideline-v0.2) on 2026-10-10.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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