Anxiety Clinical Trial
Official title:
The Influence of Information Sources on Knowledge and Anxiety in Inflammatory Bowel Disease Patients
Inflammatory Bowel Diseases (IBD) are life-long, incurable illnesses that can have a
profound effect on the patients quality of life. Disease education is a corner stone of IBD
care to enable patients to take up an active role in their disease management. While patient
education is enshrined in the IBD standards, actual patient knowledge is often poor.3
Knowledge is not associated with the level of the patient's educational achievement, but
member of patient organisations such as Crohn's and Colitis UK (CCUK) have significantly
better knowledge than non-members. This may highlight the positive effects of education
offered by CCUK, but it is also conceivable that patients with a greater interest in their
disease are more like to join organisations like CCUK. Different sources of patient
information may therefore influence what level of disease related knowledge a patient
achieves.
Apart from high quality clinical information provided by professional organisation (British
Society of Gastroenterology, European Crohn's and Colitis Organisation), the National Health
Service and charities (CORE, CCUK), there is also a host of unregulated information
available. The emerging dominance of the internet for information gathering has provided
easy access for patients to a host of websites providing information on IBD. A number of
these provide alternative (not evidence based) views, which could have a potentially
negative impact on patient's knowledge. Furthermore patients often share their stories on
internet forums and it is likely that those stories share are more likely to represent the
extreme ends of disease rather than those experienced by the majority. This could
potentially cause anxiety in patients with IBD. The quality of information found on the
internet varies widely and up to 50% of websites have been judged as poor. The vast majority
of patients with IBD have access to the internet and more than half use to search for health
related information.7 We have previously also demonstrated that patients with anxiety have
better disease related knowledge of IBD.
Status | Completed |
Enrollment | 307 |
Est. completion date | February 2016 |
Est. primary completion date | February 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: patients attending IBD clinics at Leeds Teaching Hospitals Exclusion Criteria: - Individuals who are unable to give informed consent. - Individuals who do not speak English, as the questionanire is selfadministered. - Individuals under 18 years of age. - Individuals who are attending Gastroenterology clinics at Leeds General Infirmary and St. James's University Hospital because of a flare up of disease activity of their ulcerative colitis or Crohn's disease. - Individuals with Crohn's disease who have a stoma (ileostomy), due to practical difficulties in assessing clinical activity in this patient group (it is not actually possible to calculate the HarveyBradshaw index in patients with an ileostomy). - Individuals who, in the opinion of the investigator, are not suitable to participate in the study. - Individuals who refuse to give written, informed consent to be involved. |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
United Kingdom | Leeds Teaching Hospitals NHS Trust | Leeds | Yorkshire |
Lead Sponsor | Collaborator |
---|---|
National Health Service, United Kingdom |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | CCKNOW | CCKNOW scores according to preferred information source | 12 months | No |
Secondary | HADS-A | HADS-A scores according to preferred information source | 12 months | No |
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