Inflammatory Bowel Diseases Clinical Trial
— LIBERATEOfficial title:
Behavioural Treatment for Functional Bowel Symptoms in Inflammatory Bowel Disease
Verified date | April 2023 |
Source | St Vincent's Hospital Melbourne |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The primary aim of the project is to investigate whether a behavioural training programme improves troublesome bowel symptoms, that people with inflammatory bowel disease continue to have, despite their disease being controlled by medication. The other aim is to determine if there are factors which influence how well the training programme works. People attending an Inflammatory Bowel Disease clinic in a tertiary hospital, with bothersome bowel symptoms despite disease control, will be asked to join the study. This involves 2 to 6 sessions with a pelvic floor trained physiotherapist over a period of 6 months with further follow up at 12 months..
Status | Completed |
Enrollment | 35 |
Est. completion date | December 31, 2021 |
Est. primary completion date | July 30, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - Proven history of inflammatory bowel disease - Clinical evidence of mild, stable disease or remission - Mayo score = 4, Harvey Bradshaw index = 7 - Bothersome lower bowel symptoms of any of the following: frequency, urgency, incontinence, difficult evacuation, constipation Exclusion Criteria: - Significant medical or psychiatric comorbidity that in the opinion of the investigators would interfere with bowel function or adherence to the protocol - Clinically significant narcotic or substance abuse that in the opinion of the investigators would interfere with bowel function or adherence to the protocol - Recognised eating disorder - Non- English speaking or illiterate - Pregnancy - Previous pelvic floor physiotherapy - Current participant in another trial |
Country | Name | City | State |
---|---|---|---|
Australia | St Vincent's Hospital | Fitzroy | Victoria |
Lead Sponsor | Collaborator |
---|---|
St Vincent's Hospital Melbourne |
Australia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Change in Mayo Score | Disease activity index for ulcerative colitis | From baseline to study completion (up to 12 weeks) and at 1 year | |
Other | Change in Harvey Bradshaw Index | Disease activity index for Crohn's disease | From baseline to study completion (up to 12 weeks) and at 1 year | |
Other | Patient rating of satisfaction | 7 point Likert scale rating satisfaction | At study completion , up to 12 weeks | |
Other | Change in pelvic floor muscle function | Measurement of pelvic floor muscle movement using transperineal ultrasound | From baseline to study completion (up to 12 weeks) | |
Primary | Patient rating of improvement in symptoms | Proportion of patients achieving a rating of 'moderately improved' or 'substantially improved' on a 7 point Likert scale ranging from 'substantially worse' to 'substantially improved' | At study completion, up to 12 weeks | |
Secondary | Change in Personal assessment of Constipation Symptoms (PAC-SYM) score | 12 constipation symptoms each rated on a 5 point Likert scale (0=symptom absent to 4 = very severe. | From baseline to study completion (up to 12 weeks) and at 1 year | |
Secondary | Change in St Marks Faecal Incontinence Score | Faecal incontinence symptom score ranging from 0-24 | From baseline to study completion (up to 12 weeks) and at 1 year | |
Secondary | Change in Inflammatory Bowel disease questionnaire (IBDQ) score | Disease specific quality of life instrument with 32 questions covering 4 domains - bowel symptoms, systemic symptoms, emotional function, social function | From baseline to study completion (up to 12 weeks) and at 1 year | |
Secondary | Change in Short Form -36 (SF-36) score | Generic quality of life score | From baseline to study completion (up to 12 weeks) and at 1 year | |
Secondary | Change in Hospital Anxiety and Depression Score (HADS) | 14 item questionnaire indicating presence of anxiety or depression | From baseline to study completion (up to 12 weeks) and at 1 year | |
Secondary | Change in Brief Illness Perception Questionnaire score | 9 item questionnaire designed to assess cognitive and emotional perception of illness | From baseline to study completion (up to 12 weeks) and at 1 year | |
Secondary | Change in Brief Cope score | 28 item questionnaire assessing patients' strategies for coping with stress | From baseline to study completion (up to 12 weeks) and at 1 year | |
Secondary | Change in Inflammatory Bowel Disease Self-efficacy scale (IBD-SES) | Disease specific scale with 29 items assessing how well patients believe they are managing their disease | From baseline to study completion (up to 12 weeks) and at 1 year | |
Secondary | Change in Euro-Qol (EQ-5D) | Generic quality of life tool to calculate quality adjusted life years (QALYs) | From baseline to study completion (up to 12 weeks) and at 1 year |
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