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Addressing Depression and Anxiety Symptoms in Patients With Inflammatory Bowel Disease

Primary Purpose

Inflammatory Bowel Diseases, Crohn Disease, Ulcerative Colitis

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Web-Based Cognitive Behavioral Therapy
Short Questionnaires
Nurse Monitoring
Detailed Questionnaires
Screening Form
Sponsored by
Mount Sinai Hospital, Canada
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Inflammatory Bowel Diseases

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • PHQ-9 AND/OR GAD-7 score ≥ 10
  • Confirmed diagnosis of IBD (based on record of diagnostic endoscopy)
  • Access to Computer or Smartphone
  • Access to an Internet Connection

Exclusion Criteria:

  • Patients without a record of diagnostic endoscopy in their clinical record
  • Under psychological treatment parallel to the intervention being carried out
  • Diagnosis of major depressive, dysthymic, bipolar or psychotic disorder
  • History of anti-depressant medication use within 1 month of enrollment
  • History of substance abuse or dependence within 1 month of enrollment
  • Previous course of CBT within 12 months of Enrollment
  • History of suicide
  • History of psychiatric hospitalization
  • Inability to provide informed consent
  • Insufficient command of written and spoken English

Sites / Locations

  • Mount Sinai HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Psychological Intervention

Control

Arm Description

Patients will be randomized to the intervention group after they have complete the study screening form. Patients randomized to the intervention group will receive a multifaceted intervention consisting of the following components (administered over an 8 week period): (1) Web-Based Cognitive Behavioral Therapy: (2) Short Questionnaires; (3) Ongoing Nurse Monitoring.

Patients will be randomized to the control group after they have completed the study screening form. Patients randomized to the control group will receive the usual standard of care that is available to patients with moderate anxiety or depression. Additionally, control patients will completed detailed questionnaires for assessment of primary and secondary outcomes.

Outcomes

Primary Outcome Measures

Rates of Moderate Depression (PHQ-9)
Post-intervention rates will be compared between study groups
Rates of Moderate Anxiety (GAD-7)
Post-intervention rates will be compared between study groups
Rates of Moderate Depression (PHQ-9) and co-morbid Anxiety (GAD-7)
Post-intervention rates will be compared between study groups

Secondary Outcome Measures

Difference in Depression Scores (PHQ-9)
Post-intervention Patient Health Questionnaire (PHQ-9) scores will be compared between study groups
Difference in Anxiety Scores (GAD-7)
Post-intervention Generalized Anxiety Disorder (GAD-7) scores will be compared between study groups
Change in Depression Scores (PHQ-9)
Change in Patient Health Questionnaire (PHQ-9) scores between enrollment and post-intervention will be compared within study groups
Change in Anxiety Scores (GAD-7)
Change in Generalized Anxiety Disorder (GAD-7) scores between enrollment and post-intervention will be compared within study groups
Rates of Active IBD (PRO-2 or MAYO-6)
Post-intervention rates will be compared between study groups
Rates of Active IBD (PRO-2 or MAYO-6)
Change in rates between enrollment and post-intervention will be compared within study groups
Difference in Quality of Life Scores (SIBDQ)
Post-intervention Short Inflammatory Bowel Disease Questionnaire (SIBDQ) scores will be compared between study groups
Difference in Patient Satisfaction Scores (CACHE)
Post-intervention Patient Satisfaction with Health Care in IBD (CACHE) scores will be compared between study groups
Change in Quality of Life Scores (SIBDQ)
Change in Short Inflammatory Bowel Disease Questionnaire (SIBDQ) scores between enrollment and post-intervention will be compared within study groups
Change in Patient Satisfaction Scores (CACHE)
Change in Patient Satisfaction with Health Care in IBD (CACHE) scores between enrollment and post-intervention will be compared within study groups
Rates of IBD-related hospitalizations
Event rates over trial period will be compared between study groups
Rates of IBD-related surgery over intervention period
Event rates over trial period will be compared between study groups

Full Information

First Posted
October 27, 2017
Last Updated
April 14, 2018
Sponsor
Mount Sinai Hospital, Canada
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1. Study Identification

Unique Protocol Identification Number
NCT03327038
Brief Title
Addressing Depression and Anxiety Symptoms in Patients With Inflammatory Bowel Disease
Official Title
Addressing Depression and Anxiety Symptoms in Patients With Inflammatory Bowel Disease (ADAPT-IBD)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
May 1, 2019 (Anticipated)
Study Completion Date
January 1, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Mount Sinai Hospital, Canada

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Inflammatory Bowel Diseases (IBD) are chronic debilitating disorders of the gastrointestinal tract that comprise two subtypes; Crohn's Disease (CD) and Ulcerative Colitis (UC). Canada has among the highest incidence rates of CD and UC in the world, as high as 20.2 and 19.5 per 100,000 respectively. Although, IBD can occur at any age, it is frequently diagnosed in the second and third decades of life, at a time when vulnerable individuals are entering the prime years of their lives. This age of onset, coupled with the recurrent and frequently relapsing nature of these disorders, can significantly impair the psychological well-being of patients. Therefore, it's not surprising that patients with IBD report a higher burden of depression and anxiety in comparison to the general population. The prevalence of depression and anxiety in patients with IBD have previously been linked to the following: (1) Increased risk of surgery; (2) Increased number of relapses; (3) Clinical recurrence; (4) Treatment failure and earlier retreatment; (5) Lower self-reported quality of life, satisfaction, and medication adherence; (6) and Increased health care utilization. Although, depression and anxiety are highly treatable conditions, they are often under-recognized and under- treated in patients with IBD. The most common treatments for these disorders are pharmacological agents and psychological treatments. Psychological treatments like Cognitive Behavioral Therapy (CBT) have extensive support for treatment of depression and anxiety. The major advantage of psychological treatments over pharmacological agents is their ability to sustain improved depression and anxiety symptoms in patients post-treatment. As part of this study, we aim to evaluate the following: Specific Aim #1: Determine whether a psychological intervention, involving web-based CBT, is effective in ameliorating depression and anxiety symptoms in a cohort of adult IBD patients. Specific Aim #2: Determine the durability effect of the intervention on sustaining improved psychiatric symptoms. Specific Aim #3: Determine the impact of a psychological on IBD-specific and psychiatric-specific health care utilization.
Detailed Description
Inflammatory Bowel Diseases (IBD) are chronic debilitating disorders of the gastrointestinal tract that comprise two subtypes; Crohn's Disease (CD) and Ulcerative Colitis (UC). Canada has among the highest incidence rates of CD and UC in the world, as high as 20.2 and 19.5 per 100,000 respectively. Although, IBD can occur at any age, it is frequently diagnosed in the second and third decades of life; at a time when vulnerable individuals are entering the prime years of their lives. This age of onset, coupled with the recurrent and frequently relapsing nature of these disorders, can significantly impair the psychological well-being of patients. Therefore, it's not surprising that patients with IBD report a higher burden of depression and anxiety in comparison to the general population. The rates of depression in patients with IBD, as measured by the National Population Health Survey and the Canadian Community Health Survey, range from 14.7% to 16.3%. These rates are significantly higher than the general Canadian population, in which 5.6% of healthy respondents reported a 12-month prevalence of depression. Moreover, studies among clinical samples of IBD patients have reported rates of depression as high as 35%. The prevalence of depression and anxiety in patients with IBD have previously been linked to the following: (1) Increased risk of surgery; (2) Increased number of relapses; (3) Clinical recurrence; (4) Treatment failure and earlier retreatment; (5) Lower self-reported quality of life, satisfaction, and medication adherence; (6) and Increased health care utilization. Although, depression and anxiety are highly treatable conditions, they are often under recognized and under treated in patients with IBD. The most common treatments for these disorders are pharmacological agents and psychological treatments. Psychological treatments like Cognitive Behavioral Therapy (CBT) have extensive support for treatment of depression and anxiety. CBT refers to a group of interventions that share the notion that cognitive factors influence mental disorders and psychological distress, and that maladaptive cognitions contribute to emotional distress and behavioral problems. The major advantage of psychological treatments over pharmacological agents is their ability to sustain improved depression and anxiety symptoms in patients post-treatment. Considering the prevalence and impact of depression and anxiety disorders in patients with IBD, further research in this area is needed to identify the most effective approaches for screening and treatment of these disorders. Research is also need to ascertain the effects of psychological treatments for depression and anxiety on influencing physiological aspects of IBD. As part of this study, we aim to evaluate the effectiveness of a psychological intervention which incorporates web-based CBT intervention on a cohort of adult IBD patients; by measuring its impact on clinical and self-reported outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Diseases, Crohn Disease, Ulcerative Colitis, Depression, Anxiety

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Psychological Intervention
Arm Type
Experimental
Arm Description
Patients will be randomized to the intervention group after they have complete the study screening form. Patients randomized to the intervention group will receive a multifaceted intervention consisting of the following components (administered over an 8 week period): (1) Web-Based Cognitive Behavioral Therapy: (2) Short Questionnaires; (3) Ongoing Nurse Monitoring.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Patients will be randomized to the control group after they have completed the study screening form. Patients randomized to the control group will receive the usual standard of care that is available to patients with moderate anxiety or depression. Additionally, control patients will completed detailed questionnaires for assessment of primary and secondary outcomes.
Intervention Type
Behavioral
Intervention Name(s)
Web-Based Cognitive Behavioral Therapy
Intervention Description
Patients will receive access to a 5-week web-based CBT program entitled 'Mood Gym'. The program is derived from traditional, therapist-directed cognitive behavioral therapy. The program consists of 5 modules, and patients will asked to complete 1 module per week over, during weeks 2-6 over their intervention period.
Intervention Type
Other
Intervention Name(s)
Short Questionnaires
Intervention Description
Patients will receive emails to complete bi-weekly, web-based questionnaires at weeks 2, 4, and 6 of their intervention period. The short questionnaires will ask to patients to self-report their Depression (PHQ-9) and Anxiety (GAD-7) symptoms; along with their Crohn's Disease activity (PRO-2) or Ulcerative Colitis Disease Activity (MAYO-6).
Intervention Type
Behavioral
Intervention Name(s)
Nurse Monitoring
Intervention Description
Patient responses to the short questionnaires will be monitored by an IBD advanced practice nurse. The IBD nurse will determine if there are elevations in anxiety, depression, and disease activity over the intervention period. Based on patient responses to the short questionnaires, the nurse will follow-up with patients via email or telephone to address patient symptoms. If there are clinically important changes in the patients' disease activity the nurse may also arrange for the patients to receive expedited outpatient follow-up with their gastroenterologist.
Intervention Type
Other
Intervention Name(s)
Detailed Questionnaires
Intervention Description
Patients will complete a detailed questionnaires at enrollment (i.e. week 1 of enrollment) and also at post-intervention (i.e. week 8 of enrollment). The enrollment questionnaire will query the patients Ulcerative Colitis Disease Activity (MAYO-6) or Crohn's Disease Activity (PRO-2); Quality of Life (SIBDQ); and Patient Satisfaction with Health Care in IBD (CACHE). The post-intervention questionnaire will query the same information as the enrollment questionnaire but will also ask patients to self-report their depression (PHQ-9) and anxiety (GAD-7) symptoms.Quality of Life will be measured using the 10 item Short Inflammatory Bowel Disease Questionnaire (SIBDQ), which has a total score range of 10 to 70, with higher scores indicating better quality of life. Patient Satisfaction with Health Care in IBD will be measured using the 32 item CACHE Questionnaire, which scores from 0 -least satisfaction to 100-highest satisfaction.
Intervention Type
Other
Intervention Name(s)
Screening Form
Intervention Description
Patients will complete a screening form at routine IBD outpatient visits to Mount Sinai Hospital to self-report their depression and generalized anxiety symptoms. Their depression symptoms will be reported on the 9-item Patient Health Questionnaire (PHQ-9), which has a total score ranging from 0 to 27, with scores of 5, 10, 15 and 20 representing cut points for mild, moderate, moderately severe, and severe depression. Their generalized anxiety symptoms will be reported on the 7-item Generalized Anxiety Disorder Questionnaire (GAD-7), which has a total score ranging from 0 to 21, with scores of 5, 10, and 15 representing cut points for mild, moderate, and severe anxiety. Patients who self-report scores of moderate depression AND/OR moderate anxiety will be eligible to participate in this study.
Primary Outcome Measure Information:
Title
Rates of Moderate Depression (PHQ-9)
Description
Post-intervention rates will be compared between study groups
Time Frame
Post-Intervention (i.e. week 8)
Title
Rates of Moderate Anxiety (GAD-7)
Description
Post-intervention rates will be compared between study groups
Time Frame
Post-Intervention (i.e. week 8)
Title
Rates of Moderate Depression (PHQ-9) and co-morbid Anxiety (GAD-7)
Description
Post-intervention rates will be compared between study groups
Time Frame
Post-Intervention (i.e. week 8)
Secondary Outcome Measure Information:
Title
Difference in Depression Scores (PHQ-9)
Description
Post-intervention Patient Health Questionnaire (PHQ-9) scores will be compared between study groups
Time Frame
Post-Intervention (i.e. week 8)
Title
Difference in Anxiety Scores (GAD-7)
Description
Post-intervention Generalized Anxiety Disorder (GAD-7) scores will be compared between study groups
Time Frame
Post-Intervention (i.e. week 8)
Title
Change in Depression Scores (PHQ-9)
Description
Change in Patient Health Questionnaire (PHQ-9) scores between enrollment and post-intervention will be compared within study groups
Time Frame
Between Enrollment (i.e. week 1) and Post-intervention (i.e. week 8)
Title
Change in Anxiety Scores (GAD-7)
Description
Change in Generalized Anxiety Disorder (GAD-7) scores between enrollment and post-intervention will be compared within study groups
Time Frame
Between Enrollment (i.e. week 1) and Post-intervention (i.e. week 8)
Title
Rates of Active IBD (PRO-2 or MAYO-6)
Description
Post-intervention rates will be compared between study groups
Time Frame
Post-Intervention (i.e. week 8)
Title
Rates of Active IBD (PRO-2 or MAYO-6)
Description
Change in rates between enrollment and post-intervention will be compared within study groups
Time Frame
Between Enrollment (i.e. week 1) and Post-intervention (i.e. week 8)
Title
Difference in Quality of Life Scores (SIBDQ)
Description
Post-intervention Short Inflammatory Bowel Disease Questionnaire (SIBDQ) scores will be compared between study groups
Time Frame
Post-Intervention (i.e. week 8)
Title
Difference in Patient Satisfaction Scores (CACHE)
Description
Post-intervention Patient Satisfaction with Health Care in IBD (CACHE) scores will be compared between study groups
Time Frame
Post-Intervention (i.e. week 8)
Title
Change in Quality of Life Scores (SIBDQ)
Description
Change in Short Inflammatory Bowel Disease Questionnaire (SIBDQ) scores between enrollment and post-intervention will be compared within study groups
Time Frame
Between Enrollment (i.e. week 1) and Post-intervention (i.e. week 8)
Title
Change in Patient Satisfaction Scores (CACHE)
Description
Change in Patient Satisfaction with Health Care in IBD (CACHE) scores between enrollment and post-intervention will be compared within study groups
Time Frame
Between Enrollment (i.e. week 1) and Post-intervention (i.e. week 8)
Title
Rates of IBD-related hospitalizations
Description
Event rates over trial period will be compared between study groups
Time Frame
Between Enrollment (i.e. week 1) and Post-intervention (i.e. week 8)
Title
Rates of IBD-related surgery over intervention period
Description
Event rates over trial period will be compared between study groups
Time Frame
Between Enrollment (i.e. week 1) and Post-intervention (i.e. week 8)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PHQ-9 AND/OR GAD-7 score ≥ 10 Confirmed diagnosis of IBD (based on record of diagnostic endoscopy) Access to Computer or Smartphone Access to an Internet Connection Exclusion Criteria: Patients without a record of diagnostic endoscopy in their clinical record Under psychological treatment parallel to the intervention being carried out Diagnosis of major depressive, dysthymic, bipolar or psychotic disorder History of anti-depressant medication use within 1 month of enrollment History of substance abuse or dependence within 1 month of enrollment Previous course of CBT within 12 months of Enrollment History of suicide History of psychiatric hospitalization Inability to provide informed consent Insufficient command of written and spoken English
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Geoffrey C Nguyen, MD, PhD
Phone
(416) 586-4800
Ext
2819
Email
geoff.nguyen@utoronto.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Geoffrey C Nguyen, MD, PhD
Organizational Affiliation
Mount Sinai Hospital (Toronto, ON, Canada)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Geoffrey C Nguyen, MD, PhD
Phone
(416) 586-4800
Ext
2819
Email
geoff.nguyen@utoronto.ca

12. IPD Sharing Statement

Citations:
PubMed Identifier
27069364
Citation
Yanartas O, Kani HT, Bicakci E, Kilic I, Banzragch M, Acikel C, Atug O, Kuscu K, Imeryuz N, Akin H. The effects of psychiatric treatment on depression, anxiety, quality of life, and sexual dysfunction in patients with inflammatory bowel disease. Neuropsychiatr Dis Treat. 2016 Mar 24;12:673-83. doi: 10.2147/NDT.S106039. eCollection 2016.
Results Reference
background
PubMed Identifier
16863561
Citation
Bernstein CN, Wajda A, Svenson LW, MacKenzie A, Koehoorn M, Jackson M, Fedorak R, Israel D, Blanchard JF. The epidemiology of inflammatory bowel disease in Canada: a population-based study. Am J Gastroenterol. 2006 Jul;101(7):1559-68. doi: 10.1111/j.1572-0241.2006.00603.x. Erratum In: Am J Gastroenterol. 2006 Aug;101(8):1945.
Results Reference
background
PubMed Identifier
19161177
Citation
Graff LA, Walker JR, Bernstein CN. Depression and anxiety in inflammatory bowel disease: a review of comorbidity and management. Inflamm Bowel Dis. 2009 Jul;15(7):1105-18. doi: 10.1002/ibd.20873.
Results Reference
background
PubMed Identifier
22778720
Citation
Sajadinejad MS, Asgari K, Molavi H, Kalantari M, Adibi P. Psychological issues in inflammatory bowel disease: an overview. Gastroenterol Res Pract. 2012;2012:106502. doi: 10.1155/2012/106502. Epub 2012 Jun 21.
Results Reference
background
PubMed Identifier
26856938
Citation
Fiest KM, Walker JR, Bernstein CN, Graff LA, Zarychanski R, Abou-Setta AM, Patten SB, Sareen J, Bolton JM, Marriott JJ, Fisk JD, Singer A, Marrie RA; CIHR Team Defining the Burden and Managing the Effects of Psychiatric Comorbidity in Chronic Immunoinflammatory Disease. Systematic review and meta-analysis of interventions for depression and anxiety in persons with multiple sclerosis. Mult Scler Relat Disord. 2016 Jan;5:12-26. doi: 10.1016/j.msard.2015.10.004. Epub 2015 Oct 19.
Results Reference
background
PubMed Identifier
16917224
Citation
Fuller-Thomson E, Sulman J. Depression and inflammatory bowel disease: findings from two nationally representative Canadian surveys. Inflamm Bowel Dis. 2006 Aug;12(8):697-707. doi: 10.1097/00054725-200608000-00005.
Results Reference
background
PubMed Identifier
23459093
Citation
Hofmann SG, Asnaani A, Vonk IJ, Sawyer AT, Fang A. The Efficacy of Cognitive Behavioral Therapy: A Review of Meta-analyses. Cognit Ther Res. 2012 Oct 1;36(5):427-440. doi: 10.1007/s10608-012-9476-1. Epub 2012 Jul 31.
Results Reference
background
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

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Addressing Depression and Anxiety Symptoms in Patients With Inflammatory Bowel Disease

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