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Effect of Enhanced Interactive Text Messages and Phone Instruction on the Quality of Bowel Preparation for Colonoscopy.

Not Applicable
Conditions
Colon Polyp
Colon Neoplasm
Interventions
Other: Enhanced bowel preparation instruction
Registration Number
NCT04898426
Lead Sponsor
Griffith Base Hospital
Brief Summary

Efficacy Evaluation of Enhanced Bowel Preparation Instructions in Elective Colonoscopy.

Detailed Description

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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
500
Inclusion Criteria
  • Elective colonoscopy booking at Griffith Base Hospital.
Exclusion Criteria
  • Emergency colonoscopy
  • Patients who are unable to understand bowel preparation instructions in the following languages: English, Italian, Punjabi, Gujarati, Samoan, Mandarin.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Enhanced Bowel Preparation InstructionEnhanced bowel preparation instructionPatients receive enhanced instructions (SMS, phone call, info website) in addition to the standard-of-care bowel preparation instruction.
Primary Outcome Measures
NameTimeMethod
Bowel preparation qualityBowel 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.

Bowel preparation quality is assessed using the Boston Bowel Preparation Scale (range 0 to 9, with higher scores indicating better bowel preparation quality)

Secondary Outcome Measures
NameTimeMethod
Polyp detection ratePolyp detection rate will be calculated at the time of study completion, expected to be 12 months.

The proportion of colonoscopies in which a polyp was detected. The rates will be compared between the study groups.

Colonoscopy cancellation rateColonoscopy cancellation rate will be calculated at the time of study completion, expected to be 12 months.

The number of colonoscopy being cancelled within 48 hours of the colonoscopy date. The rates will be compared between the study groups.

Caecal intubation rateCaecal intubation rate will be calculated at the time of study completion, expected to be 12 months.

The proportion of colonoscopies in which the colonoscope reaches the furthest extent of the colon. The rates will be compared between the study groups.

Trial Locations

Locations (1)

Griffith Base Hospital

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Griffith, New South Wales, Australia

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