Trial Details

Not Recruiting
Basic Information
Clinical ID c3310
Identifier NL-OMON32226
Trial Title Enhancing the quality of life of patients with inflammatory bowel disease; a multicentre study investigating cognitive behavioral therapy - CBT and IBD
Trial URL Visit Original Page
Study Information
Study Results

No results available

Conditions geringe kwaliteit van leven, angst en depressie klachten Inflammatory bowel disease;10017943
Interventions Intervention The intervention spans an 8-week period, consisting of eight weekly sessions, each lasting one hour. The cognitive behavioral therapy will be conducted by registered psychotherapists, specialized in conducting cognitive behavioral therapy. The first session will focus on the rationale of cognitive behavioral therapy, i.e. the influence of (irrational or dysfunctional) cognitions and attitudes on (maladaptive) feelings and behaviors. Additionally, goal setting will be initiated. These therapy goals will be unique for each patient. The subsequent sessions (2-6) will be targeted at identifying and amending irrational cognitions and attitudes related to IBD. Each session will address specific illness-related cognitions. Additionally, patients will be taught how dysfunctional cognitions and attitudes affect adversely feelings and behaviors. These dysfunctional cognitions and attitudes will be challenged and replaced by functional cognitions and attitudes. After each session, patients will be given home work. For example, patients will be asked to register negative experiences, and accompanying cognitions, feelings and behaviors. Clearly, some of the negative cognitions are realistic and reflect the limitations that the disease imposes. Such thoughts will be worked through, accepted or resolved. Finally, in the last two sessions, the newly learned cognitions and attitudes will be consolidated.
Participant Information
Sponsor Academisch Medisch Centrum
City -
Country/Region Netherlands
Enrollment Criteria
Sex Requirement NOT SPECIFIED
Age Requirement ADULT, ELDER, OLDER_ADULT
Study Design
Study Type Interventional
Phase Not Available
Time Information
Start Date 2025-04-24
Primary Completion Date -
Completion Date -