- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03565263
Functional Gastrointestinal Disorders in Pediatric IBD (TFI-MICI)
Functional Gastrointestinal Disorders in Children and Adolescents With Inflammatory Bowel Disease in Remission: Prevalence and Identification of Clinical and Psychosocial Risk Factors
Background: Persistent gastrointestinal symptoms have been described in patients who are considered in remission of their inflammatory bowel disease (IBD). These symptoms, attributed to Functional gastrointestinal disorders (FGID) in IBD, may have a significant impact of quality of life, and may be associated with fatigue, anxiety and depression. There is very little data regarding pediatric specificities of these FGID.
Aims: The aim of the study is to evaluate the prevalence of FGID in pediatric patients with IBD in remission. Secondary aims are to investigate a possible association of FGID with fatigue, anxiety, depression and impacted quality of life in the patients, as well as anxiety and depression in the parents.
Methods: This will be an observational, case-control study. All patients between 9 and 18 years old , with IBD in remission will be invited to participate. Questionnaires will be web-based and will evaluate: presence of FGID (Fr-qPGS), fatigue (FACIT-F), anxiety (SCARED-R), depression (CDI), quality of life (IMPACT-III). Parents will be invited to fill in web-based questionnaires on their symptoms of anxiety (STAI/Y-A and STAI/Y-B) and depression (BDI). Clinical parameters will be retrieved retrospectively from the chart. Level of remission will be confirmed by most recent blood tests and fecal calprotectin. Patients with FGID will be compared to patients without FGID in terms of clinical characteristics, disease phenotype and associated psychological comorbidities.
Studieöversikt
Status
Studietyp
Inskrivning (Faktisk)
Kontakter och platser
Studieorter
-
-
-
Caen, Frankrike
- Caen University hospital
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
In the aim of recruiting a sample that will be the most representative possible of the population of pediatric IBD patients in remission in France, patients will be recruited for the study through different procedures:
- either during a routine visit to the pediatric gastroenterology clinic (all French pediatric gastroenterology clinics will be study centers)
- or during a routine visit to the adult gastroenterology clinic (the French adult gastroenterologists will be informed of the study and will be able to apply to be a study center)
- finally, the patient will be able to find information on the study through the French IBD patient Foundation (association Francois Aupetit) and contact the investigators in order to participate.
Beskrivning
Inclusion Criteria:
- IBD (Crohns disease, Ulcerative colitis or IBD-U)
- in remission (defined as: Physician's global assessment = remission, no nocturnal stools, no blood in stools, < or = 3 stools/day, C reactive protein < 10 mg/L, erythrocyte sedimentation rate < 20 mm, no flare of disease or change of treatment in the last 3 months, no ongoing corticosteroid therapy
- followed for IBD for at least 1 year
Exclusion Criteria:
- presence of an ileostomy or colostomy
- past history of total colectomy
- unable to understand written French or to answer the questionnaires
Studieplan
Hur är studien utformad?
Designdetaljer
- Observationsmodeller: Case-Control
- Tidsperspektiv: Tvärsnitt
Kohorter och interventioner
Grupp / Kohort |
|---|
|
FGID-IBD
|
|
No FGID-IBD
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Presence of Functional Gastrointestinal Disorder
Tidsram: baseline
|
Rome III criteria for FGID (Fr-qPGS questionnaire)
|
baseline
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Anxiety
Tidsram: baseline
|
SCARED-R questionnaire
|
baseline
|
|
Depression
Tidsram: baseline
|
CDI questionnaire
|
baseline
|
|
Quality of life - disease related
Tidsram: baseline
|
IMPACT-III questionnaire
|
baseline
|
|
Fatigue
Tidsram: baseline
|
peds FACIT-F questionnaire
|
baseline
|
|
Anxiety (parents)
Tidsram: baseline
|
STAI/Y-A and STAI/Y-B questionnaires
|
baseline
|
|
Depression (parents)
Tidsram: baseline
|
BDI questionnaire
|
baseline
|
Samarbetspartners och utredare
Sponsor
Utredare
- Huvudutredare: Claire Dupont-Lucas, Groupe d'Etudes Therapeutiques des Affections Inflammatoires Digestives pediatriques
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 17-160
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
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