A randomized control trial of a brief educational intervention on colonoscopy preparation in inflammatory bowel disease
Not Applicable
- Conditions
- Health Condition 1: K50- Crohns disease [regional enteritis]Health Condition 2: K51- Ulcerative colitis
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with inflammatory bowel disease undergoing colonoscopy for mapping of disease extent or dysplasia screening
Exclusion Criteria
Contraindications for colonoscopy eg active disease precluding colonoscopy, acute obstruction
Suspected stricturing disease on previous imaging or clinical symptoms
Severe systemic illness- symptomatic heart failure, CTP -C cirrhosis, chronic kidney disease with GFR < 30
Unwilling to participate
Pregnant and breastfeeding females
Psychiatric co morbidities (clinical depression, bipolar disorder or schizophrenia)
Re procedure for a patient already randomized or already included in a trial
Patients undergone an abdominal surgery in the past related to bowel disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Adequate bowel preparation as defined using Boston bowel preparation score of 6 or moreTimepoint: baseline on day of colonoscopy
- Secondary Outcome Measures
Name Time Method Anxiety as assessed by GAD-7 scoreTimepoint: 14 days;Perfect bowel preparation as defined using Boston bowel preparation score of 9Timepoint: Day Zero;Satisfaction with bowel preparationTimepoint: Day zero;Time to cecal intubation <br/ ><br> <br/ ><br>Timepoint: zero day;Tolerance of bowel preparationTimepoint: Day zero;Tolerance of procedureTimepoint: 14 days;Willingness to undergo colonoscopy again if neededTimepoint: 14 days;Worsening of disease activity as per increase in SCCAI or HBI scoreTimepoint: 14 days