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Healthy Approach to Physical and Psychological Problems in Youngsters With IBD (HAPPY-IBD). (HAPPY-IBD)

Primary Purpose

Inflammatory Bowel Disease (IBD), Ulcerative Colitis, Crohn's Disease

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Cognitive behavioral therapy
Sponsored by
Erasmus Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inflammatory Bowel Disease (IBD) focused on measuring Inflammatory bowel disease (IBD), Ulcerative colitis, Crohn's disease, Children, Adolescents, Anxiety, Depression, Cognitive behavioral therapy

Eligibility Criteria

10 Years - 20 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients between 10-25 years with diagnosed IBD
  • Informed consent or assent by patients and (if necessary) parents

Exclusion Criteria:

  • IBD patients with parental report of mental retardation
  • IBD patients receiving psychopharmacological treatment (antidepressants or benzodiazepines) for depression or anxiety
  • No mastery of the Dutch language
  • IBD patients with diagnosed: Bipolar disorder, Schizophrenia/psychotic disorder, Autism spectrum disorders, Obsessive-compulsive disorder, Posttraumatic stress disorder/Acute stress disorder, or Substance use disorder
  • Physician reported substance abuse (alcohol, drugs) in the past month
  • Clinician reported Selective mutism
  • IBD patients already participating in an (psychological of psychopharmacological) intervention study
  • IBD patients who received 8 sessions of manualized cognitive behavioral therapy last year
  • current psychological treatment

Sites / Locations

  • Erasmus Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Care as usual

Cognitive Behavioral Therapy

Arm Description

Care as usual means receiving their regular medical care. This consists of the regular follow up visits at the gastroenterologist every 3 months.

The intervention group receives regular medical care (care as usual) AND a cognitive behavioral therapy program called PASCET-PI. The therapy sessions will be performed by trained psychologist.

Outcomes

Primary Outcome Measures

Reduction in symptoms of depression (change from baseline)
Measured by the Child Depression Inventory (CDI (10-17 years), Beck Depression Inventory (BDI; 18-25 years) and severity rating (interview): the Children's Depression Rating Scale (CDRS;10-12 years) and Adolescent Depression Rating Scale(ADRS;13-20 years), HAM-D: Hamilton Depression Rating Scale (21-25 year)

Secondary Outcome Measures

Reduction in symptoms of anxiety (change from baseline)
Measured by SCARED-NL: Screen for Anxiety Related Emotional Disorders (10-20 years), Hospital Anxiety and Depression Scale (HADS; 21-25 year) and severity rating by Pediatrix Anxiety Rating Scale (PARS) (10-20 years) ,Hamilton Anxiety Rating (HAM-A)(21-25 year)
General Quality of Life
Assessed by the Child Health Related Quality of Life (TACQOL) (10-15 years) Adult Health Related Quality of Life (TAAQOL, 16-25 years)
Social Skills
Assessed by Social Skills Rating System (SSRS) (10-20years) Novotni SSC: Social Skills Checklist (21-25 year)
Social competence
Assessed by Youth Self Report (YSR) / Adult Self Report (ASR)
Disease specific quality of life
Assessed by the IMPACT-III-NL (10-20years) IBDQ: Inflammatory Bowel Disease Questionnaire (21-25 year)
Disease Activity
Assessed by the Pediatric Ulcerative Colitis Activity Index (PUCAI) (10-20 years) Pediatric Crohn's Disease Activity Index (PCDAI) (10-20 years) CDAI: Crohn's Disease Activity Index (21-25 years) Partial Mayo Score (21-25 years) Physician Global Assessment (PGA)
Clinical relapse (number of flares)
10-20 Years: Relapse for CD is defined as PCDAI>30 or an increase of>15 points and intensification of medical treatment. Relapse for UC is defined as PUCAI > 34 or an increase of ≥20 points for UC and intensification of medical treatment. 21-25 years: Partial Mayo score of 3 or higher with intensification of medical treatment Or CDAI≥ 150 and an increase in baseline CDAI score of ≥ 70 points and intensification of medical treatment
Maintaining remission
Remission is defined as PCDAI < 10 for CD and PUCAI < 10 for UC. CDAI < 150 and Mayo score ≤2 with no individual subscore > 1
Medication Usage (change from baseline)
Type and dosage of medication
Necessity of surgical intervention
Description of type and extent of surgical intervention
Adherence to therapy (change from baseline)
Assessed by the Morisky Medical Adherence Scale (MASS-8)
Health care utilization (change from baseline)
Assessed by standardized items derived from the questionnaires and Report of the treating physician.
Inflammatory markers
Inflammatory markers will be measured at all time points (baseline and after 3,6,12 months) Inflammatory markers like BSE, CRP, faecal calprotectin

Full Information

First Posted
October 10, 2014
Last Updated
July 26, 2022
Sponsor
Erasmus Medical Center
Collaborators
Reinier de Graaf Groep, Albert Schweitzer Hospital, Maasstad Hospital, Haga Hospital, Amphia Hospital, Leiden University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02265588
Brief Title
Healthy Approach to Physical and Psychological Problems in Youngsters With IBD (HAPPY-IBD).
Acronym
HAPPY-IBD
Official Title
Reducing Symptoms of Depression and Anxiety in Adolescents With Inflammatory Bowel Disease in Order to Improve Quality of Life and the Clinical Course of Disease.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
September 2014 (Actual)
Primary Completion Date
October 1, 2016 (Actual)
Study Completion Date
August 24, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Erasmus Medical Center
Collaborators
Reinier de Graaf Groep, Albert Schweitzer Hospital, Maasstad Hospital, Haga Hospital, Amphia Hospital, Leiden University Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The presented study aims to reduce symptoms of depression and anxiety in adolescents with inflammatory bowel disease and increased symptoms of anxiety and depression by using the disease specific CBT program (PASCET-PI)in order to improve quality of life and to improve the clinical course of disease.
Detailed Description
Objective: The primary objective is to determine the efficacy of a disease specific cognitive behavioral therapy program in adolescents with IBD and increased symptoms of depression or anxiety on reducing symptoms of depression. Secondary objectives are to assess the effect of the CBT program on a) the clinical course of disease b) reducing symptoms of anxiety, and c) improving quality of life. We also aim to identify psychosocial and medical factors that predict or moderate the treatment response to CBT in adolescent with IBD. Study design: The presented study is a multicenter randomized controlled trial (RCT), involving CBT versus care as usual (CAU), in young IBD patients with increased symptoms of self-reported depression or anxiety. There will be three follow-up moments, after 3 months or after the intervention and after 6 and 12 months. Study population: Patients with IBD between 10-25 years and increased symptoms of depression or anxiety. We aim to include 100 patients, from which 50 patients will be randomized to the treatment condition (CBT and CAU) and 50 to the control group (CAU). Intervention: A disease specific CBT program called PASCET-PI. The control group (CAU),will receive routine medical treatment (thus no additional psychosocial intervention) and will maintain their regular follow up visits at the gastroenterologist every 3 months. Main study endpoints: Main outcome is reduction in symptoms of depression. Important secondary outcomes are the presence of clinical relapse and reduction of symptoms of anxiety. Other secondary outcomes, amongst others, are IBD activity scores, quality of life, psychosocial functioning, and adherence to medical treatment. Nature and extent of the burden and risks associated with participation, benefit and group relatedness: At first, patients with IBD 10 -25 years of age will be screened for symptoms of depression and anxiety at T1. Patients with increased symptoms of self-reported depression or anxiety (scoring above an age and gender specific cut-off score for increased depressive or anxiety symptoms) are asked to participate in the RCT. For all included patients, 4 study visits will take place, these will be combined with regular checkup visits at the gastroenterologist. Questionnaires will need to be filled in online, taking approximately 1.5 hour per assessment for patients and approximately 1 hour per assessment for parents. At baseline a psychiatric assessment interview will be executed by an independent research clinical psychologist by phone (20 minutes). The same research clinical psychologist will conduct a short psychiatric assessment interview at the follow up visits 10minutes). At baseline and after 3 months blood samples (when patients undergo routine venous punctures) will be drawn. For patients in the CBT group, 13 sessions (6 outpatient sessions, 7 by phone) and three parental sessions will take place in a hospital close to their home. Our study population consists of adolescents and young adults with IBD, as this is a specific group with high reported symptoms of depression and anxiety, therefore they will most likely benefit from the intervention. The risks associated with participation can be considered negligible and the burden minimal. For the time investment of completing the questionnaires participants will receive an incentive of 25 euro after the final assessment, which will be communicated at the start.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Disease (IBD), Ulcerative Colitis, Crohn's Disease, Anxiety, Depression
Keywords
Inflammatory bowel disease (IBD), Ulcerative colitis, Crohn's disease, Children, Adolescents, Anxiety, Depression, Cognitive behavioral therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Care as usual
Arm Type
No Intervention
Arm Description
Care as usual means receiving their regular medical care. This consists of the regular follow up visits at the gastroenterologist every 3 months.
Arm Title
Cognitive Behavioral Therapy
Arm Type
Experimental
Arm Description
The intervention group receives regular medical care (care as usual) AND a cognitive behavioral therapy program called PASCET-PI. The therapy sessions will be performed by trained psychologist.
Intervention Type
Behavioral
Intervention Name(s)
Cognitive behavioral therapy
Intervention Description
A disease specific cognitive behavioral therapy program called PASCET-PI: The PASCET-PI model focuses on behavioral activation, cognitive restructuring and problem solving skills to change maladaptive behaviors, cognitions and coping strategies specific for IBD.
Primary Outcome Measure Information:
Title
Reduction in symptoms of depression (change from baseline)
Description
Measured by the Child Depression Inventory (CDI (10-17 years), Beck Depression Inventory (BDI; 18-25 years) and severity rating (interview): the Children's Depression Rating Scale (CDRS;10-12 years) and Adolescent Depression Rating Scale(ADRS;13-20 years), HAM-D: Hamilton Depression Rating Scale (21-25 year)
Time Frame
12 weeks and 52 weeks
Secondary Outcome Measure Information:
Title
Reduction in symptoms of anxiety (change from baseline)
Description
Measured by SCARED-NL: Screen for Anxiety Related Emotional Disorders (10-20 years), Hospital Anxiety and Depression Scale (HADS; 21-25 year) and severity rating by Pediatrix Anxiety Rating Scale (PARS) (10-20 years) ,Hamilton Anxiety Rating (HAM-A)(21-25 year)
Time Frame
12 weeks and 52 weeks
Title
General Quality of Life
Description
Assessed by the Child Health Related Quality of Life (TACQOL) (10-15 years) Adult Health Related Quality of Life (TAAQOL, 16-25 years)
Time Frame
12 weeks and 52 weeks
Title
Social Skills
Description
Assessed by Social Skills Rating System (SSRS) (10-20years) Novotni SSC: Social Skills Checklist (21-25 year)
Time Frame
12 weeks
Title
Social competence
Description
Assessed by Youth Self Report (YSR) / Adult Self Report (ASR)
Time Frame
12 weeks
Title
Disease specific quality of life
Description
Assessed by the IMPACT-III-NL (10-20years) IBDQ: Inflammatory Bowel Disease Questionnaire (21-25 year)
Time Frame
12 weeks and 52 weeks
Title
Disease Activity
Description
Assessed by the Pediatric Ulcerative Colitis Activity Index (PUCAI) (10-20 years) Pediatric Crohn's Disease Activity Index (PCDAI) (10-20 years) CDAI: Crohn's Disease Activity Index (21-25 years) Partial Mayo Score (21-25 years) Physician Global Assessment (PGA)
Time Frame
52 weeks
Title
Clinical relapse (number of flares)
Description
10-20 Years: Relapse for CD is defined as PCDAI>30 or an increase of>15 points and intensification of medical treatment. Relapse for UC is defined as PUCAI > 34 or an increase of ≥20 points for UC and intensification of medical treatment. 21-25 years: Partial Mayo score of 3 or higher with intensification of medical treatment Or CDAI≥ 150 and an increase in baseline CDAI score of ≥ 70 points and intensification of medical treatment
Time Frame
52 weeks
Title
Maintaining remission
Description
Remission is defined as PCDAI < 10 for CD and PUCAI < 10 for UC. CDAI < 150 and Mayo score ≤2 with no individual subscore > 1
Time Frame
52 weeks
Title
Medication Usage (change from baseline)
Description
Type and dosage of medication
Time Frame
52 weeks
Title
Necessity of surgical intervention
Description
Description of type and extent of surgical intervention
Time Frame
52 weeks
Title
Adherence to therapy (change from baseline)
Description
Assessed by the Morisky Medical Adherence Scale (MASS-8)
Time Frame
52 weeks
Title
Health care utilization (change from baseline)
Description
Assessed by standardized items derived from the questionnaires and Report of the treating physician.
Time Frame
52 weeks
Title
Inflammatory markers
Description
Inflammatory markers will be measured at all time points (baseline and after 3,6,12 months) Inflammatory markers like BSE, CRP, faecal calprotectin
Time Frame
baseline and 12, 24 and 52 weeks
Other Pre-specified Outcome Measures:
Title
Disease perception (change from baseline)
Description
Assesses by the Brief Illness Perceptions Questionnaire (B-IPQ)
Time Frame
12 weeks
Title
Cognitive coping styles (change from baseline)
Description
Assesses by the Cognitive Emotion Regulation Questionnaire (CERQ)
Time Frame
12 weeks
Title
Quality of sleep (change from baseline)
Description
Assesses by the Sleep Self-Report (SSR) (10-20 years) PSQI: Pittsburgh Sleep Quality Index (21-25 year)
Time Frame
12 weeks
Title
Demographic factors
Description
Assesses by the Rotterdam's quality of life interview
Time Frame
12 weeks
Title
Parental anxiety and depression
Description
Assesses by the Depression, Anxiety and Stress Scale (DASS-21)
Time Frame
12 weeks
Title
Life Events
Description
Assesses by the Life events questionnaire from CERQ
Time Frame
12 weeks
Title
Family Functioning (change from baseline)
Description
Assesses by the Family Assessment Device (FAD)
Time Frame
12 weeks
Title
Disease phenotypes
Description
Assessed by the Paris Classification
Time Frame
52 weeks
Title
Treatment Strategy
Description
The treatment strategy, type and dosage of medication will be extracted from the medical file and report of the treating physician.
Time Frame
52 weeks
Title
White blood cell RNA expression profiles (change from baseline)
Description
Assessing immune status is done by analyzing gene expression profiles in peripheral blood leukocytes. This will be performed
Time Frame
12 weeks
Title
Immunological activity in peripheral blood mononuclear cells (PBMC)
Description
A blood sample will be taken in all patients included within the Erasmus MC for determination of responsiveness of peripheral blood lymphocytes before and directly after the intervention
Time Frame
12 weeks
Title
Irritable bowel syndrome -like symptoms
Description
Assessed by the ROME III diagnostic criteria for IBS in pediatric IBD patients
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients between 10-25 years with diagnosed IBD Informed consent or assent by patients and (if necessary) parents Exclusion Criteria: IBD patients with parental report of mental retardation IBD patients receiving psychopharmacological treatment (antidepressants or benzodiazepines) for depression or anxiety No mastery of the Dutch language IBD patients with diagnosed: Bipolar disorder, Schizophrenia/psychotic disorder, Autism spectrum disorders, Obsessive-compulsive disorder, Posttraumatic stress disorder/Acute stress disorder, or Substance use disorder Physician reported substance abuse (alcohol, drugs) in the past month Clinician reported Selective mutism IBD patients already participating in an (psychological of psychopharmacological) intervention study IBD patients who received 8 sessions of manualized cognitive behavioral therapy last year current psychological treatment
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Johanna C. Escher, PhD, MD
Organizational Affiliation
Erasmus Medical Centre
Official's Role
Study Chair
Facility Information:
Facility Name
Erasmus Medical Center
City
Rotterdam
State/Province
Nederland
ZIP/Postal Code
3015CN
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
17885570
Citation
Szigethy E, Kenney E, Carpenter J, Hardy DM, Fairclough D, Bousvaros A, Keljo D, Weisz J, Beardslee WR, Noll R, DeMASO DR. Cognitive-behavioral therapy for adolescents with inflammatory bowel disease and subsyndromal depression. J Am Acad Child Adolesc Psychiatry. 2007 Oct;46(10):1290-1298. doi: 10.1097/chi.0b013e3180f6341f.
Results Reference
background
PubMed Identifier
22699797
Citation
Thompson RD, Craig A, Crawford EA, Fairclough D, Gonzalez-Heydrich J, Bousvaros A, Noll RB, DeMaso DR, Szigethy E. Longitudinal results of cognitive behavioral treatment for youths with inflammatory bowel disease and depressive symptoms. J Clin Psychol Med Settings. 2012 Sep;19(3):329-37. doi: 10.1007/s10880-012-9301-8.
Results Reference
background
PubMed Identifier
31506853
Citation
Stapersma L, van den Brink G, van der Ende J, Szigethy EM, Groeneweg M, de Bruijne FH, Hillegers MHJ, Escher JC, Utens EMWJ. Psychological Outcomes of a Cognitive Behavioral Therapy for Youth with Inflammatory Bowel Disease: Results of the HAPPY-IBD Randomized Controlled Trial at 6- and 12-Month Follow-Up. J Clin Psychol Med Settings. 2020 Sep;27(3):490-506. doi: 10.1007/s10880-019-09649-9.
Results Reference
derived
PubMed Identifier
29850915
Citation
Stapersma L, van den Brink G, van der Ende J, Szigethy EM, Beukers R, Korpershoek TA, Theuns-Valks SDM, Hillegers MHJ, Escher JC, Utens EMWJ. Effectiveness of Disease-Specific Cognitive Behavioral Therapy on Anxiety, Depression, and Quality of Life in Youth With Inflammatory Bowel Disease: A Randomized Controlled Trial. J Pediatr Psychol. 2018 Oct 1;43(9):967-980. doi: 10.1093/jpepsy/jsy029. Erratum In: J Pediatr Psychol. 2020 Aug 1;45(7):825.
Results Reference
derived
PubMed Identifier
26966551
Citation
van den Brink G, Stapersma L, El Marroun H, Henrichs J, Szigethy EM, Utens EM, Escher JC. Effectiveness of disease-specific cognitive-behavioural therapy on depression, anxiety, quality of life and the clinical course of disease in adolescents with inflammatory bowel disease: study protocol of a multicentre randomised controlled trial (HAPPY-IBD). BMJ Open Gastroenterol. 2016 Mar 2;3(1):e000071. doi: 10.1136/bmjgast-2015-000071. eCollection 2016.
Results Reference
derived

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Healthy Approach to Physical and Psychological Problems in Youngsters With IBD (HAPPY-IBD).

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