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1.
Health Educ Res ; 31(6): 782-791, 2016 12.
Article in English | MEDLINE | ID: mdl-27651394

ABSTRACT

Although inflammatory bowel disease (IBD) affects patients' psychological well-being, previous educational programs have failed to demonstrate effects on psychosocial outcomes and quality of life. Therefore, we developed a group-based psychoeducational program that combined provision of both medical information and psychological self-management skills, delivered in an interactive manner, and evaluated it in a large, cluster-randomized trial. We assigned 540 rehabilitation inpatients suffering from IBD (mean age 43 years, 66% female) to either the new intervention or a control group comprising the same overall intensity and the same medical information, but only general psychosocial information. The primary outcome was patient-reported IBD-related concerns. Secondary outcomes included disease knowledge, coping, self-management skills, fear of progression, anxiety, depression and quality of life. Assessments took place at baseline, end of rehabilitation and after 3 and 12 months.The psychoeducational self-management program did not prove superior to the control group regarding primary and secondary outcomes. However, positive changes over time occurred in both groups regarding most outcomes. The superior effectiveness of the newly developed psychoeducational program could not be demonstrated. Since the intervention and control groups may have been too similar, this trial may have been too conservative to produce between-group effects.


Subject(s)
Inflammatory Bowel Diseases/rehabilitation , Patient Education as Topic/methods , Self-Management/education , Adaptation, Psychological , Adult , Female , Health Knowledge, Attitudes, Practice , Humans , Inflammatory Bowel Diseases/psychology , Inpatients/education , Inpatients/psychology , Male , Quality of Life
3.
Z Gastroenterol ; 46(2): 187-92, 2008 Feb.
Article in English | MEDLINE | ID: mdl-18253897

ABSTRACT

BACKGROUND: The course of Crohn's disease prior to the establishment of the diagnosis is widely unknown. Therefore, we instigated a survey amongst newly diagnosed patients. PATIENTS AND METHODS: Patients diagnosed with CD less than 12 months before enrollment were included. Data on demography, social status, time interval to diagnosis, symptoms, and health care service use were collected in a retrospective, web-based, census. Patients were contacted in cooperation with two organizations: a German patients' organization (Deutsche Morbus Crohn/Colitis ulcerosa Vereinigung e.V. [DCCV]) and a professional organization of German gastroenterologists (Berufsverband der Niedergelassenen Gastroenterologen Deutschlands e.V. [bng]). Study participation was anonymous by use of a transaction number. RESULTS: The median interval period between onset of first symptoms and diagnosis was 13 months. During this time, participants reported having five doctor consultations on average, with 44% of them having a mean of 1.5 hospitalizations. 65% were unfit for work with a 14 day median (2 to 480 days) due to their symptoms. A mean (+/-SD) of 8.6 (+/-7.1) diagnostic tests were performed before the diagnosis was established. Overall health state was judged as temporarily bad or very bad by 84% of the participants. Age at diagnosis, characteristic symptoms, and localization of the disease for the participants did not differ from previously reported international data. DISCUSSION: This web-based survey shows a substantial time interval of over one year until diagnosis of Crohn's disease amongst the study participants. This period is characterized by both psychological stress and impaired ability to work.


Subject(s)
Crohn Disease/diagnosis , Adolescent , Adult , Aged , Child , Data Collection , Data Interpretation, Statistical , Education , Employment , Feasibility Studies , Germany , Health Status , Hospitalization , Humans , Internet , Middle Aged , Pilot Projects , Retrospective Studies , Statistics, Nonparametric , Stress, Psychological/etiology , Surveys and Questionnaires , Time Factors
4.
Z Gastroenterol ; 45(4): 325-31, 2007 Apr.
Article in German | MEDLINE | ID: mdl-17427117

ABSTRACT

It has been assumed that cancer surveillance colonoscopy in patients with ulcerative colitis is not conducted according to the guidelines in Germany. An inquiry of the self-help organisation German Crohn's Disease/Ulcerative Colitis Association (DCCV) among organisation members belonging to colorectal cancer risk groups confirmed that the number of biopsies taken during colonoscopy is less than that proposed by the guidelines. Only with 9.2 % of the risk group did a guideline-conformal colonoscopy take place. In more than 50 % of the cases less than 10 biopsies were taken.


Subject(s)
Colitis, Ulcerative/diagnosis , Colonic Neoplasms/diagnosis , Colonoscopy , Crohn Disease/diagnosis , Guideline Adherence , Mass Screening , Precancerous Conditions/diagnosis , Biopsy , Colitis, Ulcerative/pathology , Colon/pathology , Colonic Neoplasms/pathology , Colonic Neoplasms/prevention & control , Crohn Disease/pathology , Follow-Up Studies , Germany , Humans , Intestinal Mucosa/pathology , Precancerous Conditions/pathology , Precancerous Conditions/prevention & control , Quality Assurance, Health Care , Risk Factors
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