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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04491565
Other study ID # 201909053
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 13, 2019
Est. completion date February 7, 2020

Study information

Verified date July 2020
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators aimed to determine whether an interactive, online educational platform could improve procedure show rates and bowel preparation scores in an outpatient population presenting for routine colonoscopy.


Description:

The investigators performed a prospective, endoscopist-blinded, randomized controlled trial at a hospital-based outpatient endoscopy center. Eligible patients were randomized to two groups. Both groups received verbal and written instructions per standard care, while the intervention group received access to an interactive, on-line video. Primary outcomes were bowel preparation scores graded using the Boston Bowel Prep Score (BBPS), procedure show rates, patient satisfaction, and pre-procedure anxiety. Secondary outcomes included adenoma detection rate, mean bowel prep score per colonic segment, total number of polyps detected, and complication rates.


Recruitment information / eligibility

Status Completed
Enrollment 270
Est. completion date February 7, 2020
Est. primary completion date February 7, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- English speaking

- Access to text messaging and the internet (mobile phone access alone was considered sufficient)

- Prescribed standard split-dose bowel preparation

- Able to provide informed consent via telephone.

Exclusion Criteria:

- Pregnant

- Mentally impaired

- Undergoing screening or surveillance for inflammatory bowel disease .

Study Design


Related Conditions & MeSH terms


Intervention

Other:
educational video
an interactive educational video was viewed by participants in the intervention arm.

Locations

Country Name City State
United States Washington University in St. Louis Saint Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Adequacy of bowel prep adequacy of colonoscopy bowel prep was scored from 0 (worst) to 9 (best). intra procedure
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