Efficacy Evaluation of Enhanced Bowel Preparation Instructions in Elective Colonoscopy.
This is a prospective, randomized, controlled clinical investigation designed to evaluate the efficacy of enhanced bowel preparation instructions (automated SMS, information website, and pre-recorded phone call) in improving bowel preparation quality in elective colonoscopy. Subjects from the interventional and control group will receive standard of care bowel preparation instruction. The interventional group will receive enhanced instructions delivered by automated SMS, information website and pre-recorded phone calls in the 48 hours leading up to the colonoscopy day. The intention is to provide a reminder, to reiterate instruction on clear fluid diet and timing of bowel preparation medication, and to provide additional graphical illustration on the information website. Subjects in the interventional group must reply "OK" to each automated SMS or press "1" on the keypad at the end of the automated phone call to acknowledge understanding and receipt of instruction. Failure to acknowledge trigger an alert for a booking office staff member to directly call the patient and confirm compliance. The clinical investigation will be conducted at one hospital in the state of New South Wales, Australia. Subjects will be randomized to the interventional group (enhanced instruction) versus the control group (standard instruction). The proceduralist assessing outcome measures at the time of colonoscopy is blinded to the intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
Enrollment
500
Automated delivery of SMS, pre-recorded phone call, and link to an information website.
Griffith Base Hospital
Griffith, New South Wales, Australia
RECRUITINGBowel preparation quality
Bowel preparation quality is assessed using the Boston Bowel Preparation Scale (range 0 to 9, with higher scores indicating better bowel preparation quality)
Time frame: Bowel preparation quality is scored once for each patient at the time of colonoscopy completion. We expect to conduct this score in 500 patients over the study period of approximately 12 months.
Colonoscopy cancellation rate
The number of colonoscopy being cancelled within 48 hours of the colonoscopy date. The rates will be compared between the study groups.
Time frame: Colonoscopy cancellation rate will be calculated at the time of study completion, expected to be 12 months.
Caecal intubation rate
The proportion of colonoscopies in which the colonoscope reaches the furthest extent of the colon. The rates will be compared between the study groups.
Time frame: Caecal intubation rate will be calculated at the time of study completion, expected to be 12 months.
Polyp detection rate
The proportion of colonoscopies in which a polyp was detected. The rates will be compared between the study groups.
Time frame: Polyp detection rate will be calculated at the time of study completion, expected to be 12 months.
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