- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07610694
Eating Disorders in Patients With IBD
Prevalence of Eating Disorders in Patients With Inflammatory Bowel Disease
Inflammatory bowel diseases (IBD) may influence eating habits and lead some patients to adopt restrictive dietary behaviours to control gastrointestinal symptoms. In some cases, these behaviours may become maladaptive and resemble eating disorders, including avoidant/restrictive food intake disorder (ARFID).
This observational cross-sectional study assesses the prevalence of eating disorder risk and ARFID risk among adult patients with IBD. Participants complete validated questionnaires evaluating eating behaviours, nutritional status, and IBD-related disability. Clinical and demographic data are also collected.
Studienübersicht
Status
Detaillierte Beschreibung
Inflammatory bowel diseases (IBD), including Crohn's disease and ulcerative colitis, are chronic relapsing conditions characterized by persistent inflammatory activity, unpredictable disease course, and recurrent gastrointestinal symptoms. These factors may substantially influence patients' dietary habits. Many patients with IBD modify or restrict their diet in an attempt to prevent symptom exacerbation or disease flares. Although dietary restriction may represent an adaptive behaviour during active disease, it may persist over time and become maladaptive.
Restrictive eating behaviours in IBD may overlap with eating disorders, including avoidant/restrictive food intake disorder (ARFID). ARFID is characterized by restrictive food intake that is not primarily driven by body image concerns, but rather by mechanisms such as fear of adverse gastrointestinal consequences, low appetite or reduced interest in eating, and avoidance of specific foods. In patients with IBD, these behaviours may contribute to nutritional impairment, psychological distress, and disability.
This observational cross-sectional study assesses the prevalence of eating disorder risk and ARFID risk among adult patients with a confirmed diagnosis of IBD. Consecutive eligible patients are enrolled during routine outpatient visits. Demographic and clinical data are collected at enrolment, including disease type, age at diagnosis, disease duration, disease phenotype, previous treatments, previous surgery, extraintestinal manifestations, current therapy, laboratory markers, and disease activity.
Eating disorder risk is assessed using the Eating Attitudes Test-26 (EAT-26). ARFID risk is evaluated using the Nine-Item Avoidant/Restrictive Food Intake Disorder Screen (NIAS-9), including its subdomains related to picky eating, low appetite or limited interest in eating, and fear of adverse consequences. Nutritional status is assessed using the Patient-Generated Subjective Global Assessment (PG-SGA). IBD-related disability is evaluated using the IBD-Disk and a modified IBD-Disk including a diet-related item.
Clinical disease activity is assessed using validated disease-specific indices, including the partial Mayo score for ulcerative colitis and the Harvey-Bradshaw Index for Crohn's disease. Endoscopic activity, when available, is evaluated using the Mayo Endoscopic Subscore for ulcerative colitis and the Simple Endoscopic Score for Crohn's Disease for Crohn's disease. The study also evaluates associations between altered eating behaviours, disease activity, malnutrition risk, dietary impairment, and IBD-related disability.
The study aims to improve the identification of patients with IBD who are at risk of maladaptive restrictive eating behaviours and who may benefit from structured nutritional or psychological assessment as part of routine IBD care. The uploaded study describes the same core design elements: adult IBD patients enrolled during routine outpatient visits, ARFID risk assessed with NIAS-9, eating disorder risk with EAT-26, nutritional status with PG-SGA, and disability with IBD-Disk/mDISK. 
Studientyp
Einschreibung (Tatsächlich)
Kontakte und Standorte
Studienorte
-
-
-
Naples, Italien, 80131
- University of Naples Federico II
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Probenahmeverfahren
Studienpopulation
Beschreibung
Inclusion Criteria:
- Adult patients aged 18 years or older.
- Confirmed diagnosis of inflammatory bowel disease, including Crohn's disease or ulcerative colitis.
- Patients evaluated during routine outpatient IBD visits.
- Ability to understand and complete the study questionnaires.
Exclusion Criteria:
- Previous diagnosis or known history of eating disorders.
- Severe unmanaged psychiatric conditions.
- Pregnancy.
- Inability to complete the questionnaires or provide reliable study information.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
Kohorten und Interventionen
Gruppe / Kohorte |
|---|
|
Adult patients diagnosed with Inflammatory Bowel Disease
Adult patients with a confirmed diagnosis of inflammatory bowel disease, including Crohn's disease or ulcerative colitis, enrolled during routine outpatient visits.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Prevalence of avoidant/restrictive food intake disorder risk among adult patients with inflammatory bowel disease
Zeitfenster: Single time point at enrolment
|
The primary outcome is the proportion of adult patients with inflammatory bowel disease who screen positive for avoidant/restrictive food intake disorder risk.
ARFID risk is assessed using the validated Nine-Item Avoidant/Restrictive Food Intake Disorder Screen (NIAS-9), which evaluates restrictive eating behaviours across three domains: picky eating, low appetite or limited interest in eating, and fear of adverse consequences.
A NIAS-9 total score of 24 or higher identifies participants at risk for ARFID.
|
Single time point at enrolment
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Prevalence of eating disorder risk among adult patients with inflammatory bowel disease
Zeitfenster: Single time point at enrolment
|
The proportion of adult patients with inflammatory bowel disease who screen positive for eating disorder risk.
Eating disorder risk is assessed using the validated Eating Attitudes Test-26 (EAT-26).
A total EAT-26 score of 20 or higher identifies participants at risk for eating disorders and indicates the need for further clinical evaluation.
|
Single time point at enrolment
|
|
Association between ARFID risk and malnutrition risk
Zeitfenster: Single time point at enrolment
|
The association between avoidant/restrictive food intake disorder risk and malnutrition risk among adult patients with inflammatory bowel disease.
ARFID risk is assessed using the Nine-Item Avoidant/Restrictive Food Intake Disorder Screen (NIAS-9), while nutritional status is evaluated using the Patient-Generated Subjective Global Assessment (PG-SGA).
A PG-SGA (ranging 0-36) score of 6 or higher identifies participants at high risk of malnutrition.
|
Single time point at enrolment
|
|
Association between avoidant/restrictive food intake disorder risk and IBD-related disability
Zeitfenster: Single time point at enrolment
|
This outcome assesses the association between avoidant/restrictive food intake disorder risk and inflammatory bowel disease-related disability.
ARFID risk is assessed using the Nine-Item Avoidant/Restrictive Food Intake Disorder Screen (NIAS-9).
IBD-related disability is assessed using the IBD-Disk (score ranging 0-100), a patient-reported instrument evaluating the impact of IBD on symptoms, daily functioning, and psychosocial well-being.
Moderate-to-severe disability is defined as an IBD-Disk score of 40 or higher.
|
Single time point at enrolment
|
Mitarbeiter und Ermittler
Sponsor
Mitarbeiter
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Psychische Störungen
- Ernährungsstörungen
- Anzeichen und Symptome, Verdauungstrakt
- Darmerkrankungen
- Erkrankungen des Verdauungssystems
- Magen-Darm-Erkrankungen
- Darmerkrankungen
- Gastroenteritis
- Colitis
- Pathologische Zustände, Anzeichen und Symptome
- Ernährungs- und Stoffwechselerkrankungen
- Anzeichen und Symptome
- Vermeidende restriktive Nahrungsaufnahmestörung
- Unterernährung
- Kolitis, Geschwür
- Morbus Crohn
- Entzündliche Darmerkrankungen
- Ernährungs- und Essstörungen
Andere Studien-ID-Nummern
- 117/2025
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Essstörungen
-
Western University, CanadaNoch keine RekrutierungeTRE (Early Time Restricted Eating) mit BCAA | eTRE (Early Time Restricted Eating)Kanada
-
Western University, CanadaUnbekannteTRE (Early Time Restricted Eating) | lTRE (Late Time Restricted Eating)Kanada
-
Shalvata Mental Health CenterUniversity of Haifa; The Touro College and University SystemUnbekanntBinge-Eating-Störung | Bulimie | Night-Eating-Syndrom
-
BTL Industries Ltd.Aktiv, nicht rekrutierendBinge-Eating-Verhalten | Verlangen nach Nahrung | Essattacken/Kontrollverlust beim EssenTschechien
-
Axsome Therapeutics, Inc.Anmeldung auf EinladungBinge-Eating-StörungVereinigte Staaten
-
BioprojetAbgeschlossen
-
Taylor RezeppaOhio UniversityNoch keine RekrutierungKörperbildstörung | Binge Eating | Körperbild | Binge-Eating-Verhalten | Essattacken/Kontrollverlust beim EssenVereinigte Staaten
-
Universiti Kebangsaan Malaysia Medical CentreAbgeschlossenBinge-Eating-VerhaltenMalaysia
-
Axsome Therapeutics, Inc.RekrutierungBinge-Eating-StörungVereinigte Staaten
-
Otsuka Pharmaceutical Development & Commercialization...AbgeschlossenBinge-Eating-StörungVereinigte Staaten