Viewing Study NCT04898426



Ignite Creation Date: 2024-05-06 @ 4:11 PM
Last Modification Date: 2024-10-26 @ 2:05 PM
Study NCT ID: NCT04898426
Status: UNKNOWN
Last Update Posted: 2021-08-16
First Post: 2021-05-11

Brief Title: Effect of Enhanced Interactive Text Messages and Phone Instruction on the Quality of Bowel Preparation for Colonoscopy
Sponsor: Griffith Base Hospital
Organization: Griffith Base Hospital

Study Overview

Official Title: Effect of Enhanced Interactive Text Messages and Phone Instruction on the Quality of Bowel Preparation for Colonoscopy a Randomised Controlled Trial
Status: UNKNOWN
Status Verified Date: 2021-08
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None