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Clinical Trials/NCT01648504
NCT01648504CompletedNot Applicable

Integration of an Electronic Education System Into Colonoscopy: Improving Education, Consent and Compliance of Patients at Colonoscopy With an Ipad-based Secure Video Intervention

Johns Hopkins University1 site in 1 country40 target enrollmentStarted: June 1, 2012Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
40
Locations
1
Primary Endpoint
Completion rate of colonoscopy procedure

Study Overview

Brief Summary

The investigators will attempt to improve the patient experience before colonoscopy. The investigators will provide an in-office ipad video series and an electronic web guide to help patients learn all the best ways to prepare for colonoscopy. The investigators will then follow the patients who receive this eGuide to colonoscopy and observe whether or not they enjoyed the additional access to information from their providers, and will monitor whether or not they were better prepared for their colonoscopy.

Detailed Description

This study would assess the ability of an e-intervention in patient education and instructions during peri-procedure and procedural day visits to improve the experience of gastroenterology procedures. This study would seek to show that through this alternative educational measure, there would be an increased show rate to colonoscopy appointments, an increased preparation quality, and an increase in patient understanding and satisfaction with the colonoscopy procedure. The investigators will attempt to track procedure completion rate and polyp detection rate for individual providers.

The e-intervention would be multimodal. In the pre-procedure setting, ipad would be able to provide a viewpoint for the video education, a template for the patients (or caregivers) to send themselves links to appropriate instructions to remind them of their obligations by secure email. This e-intervention would supplement traditional printed and website accessible instructions.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Masking
None

Eligibility Criteria

Ages
18 Years to 90 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Undergoing Colonoscopy at Johns Hopkins
  • Ages 18 to 90
  • Access to email (themselves or designee)
  • Access to internet outside of physician visit

Exclusion Criteria

  • Unable to consent
  • Unwilling to participate
  • Unable to care for themselves

Arms & Interventions

Intervention with eGuide to colonoscopy

Experimental

The investigators will prospectively enroll and follow patients who receive the eGuide to Colonoscopy and determine benefit and satisfaction with the intervention as part of a pilot study.

Intervention: eGuide to Colonoscopy and in office ipad education (Other)

Outcomes

Primary Outcomes

Completion rate of colonoscopy procedure

Time Frame: 1 day

Could the colonoscopy be completed in its entirety on the date scheduled?

Secondary Outcomes

  • preparation quality(one day)
  • adenoma detection rate by provider(6 months)
  • Patient satisfaction(3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ellen Stein, MD

Principal Investigator

Johns Hopkins University

Study Sites (1)

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