ClinicalTrials.gg
Status unknownNCT05734079Updated Feb 17, 2023

Impact of Digital Tools on the Quality of Bowel Preparation for Colonoscopy

An interventional study of Standard of care and Standard of care + Video call in Colonoscopy, sponsored by Ziv Hospital. Status unknown. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-02-17.

Sponsored by Ziv Hospital · Not applicable, Interventional, and Health services research

The sponsor has not verified this record recently (last verified Feb 2023), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
825
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This is a single blinded randomized controlled study. The main question of this study is whether better preparation by making full use of digital tools can increase patient compliance with the preparation methods for colonoscopy, and as a result improve bowel preparation quality and colonoscopy outcomes in a cost-effective manner.

Participants will randomly assigned to one of three colonoscopy preparation groups (i) a written hand out containing all information required for bowel preparation (standard care) (ii) standard care and in addition a video call with a professional nurse conducted via digital devices and a free software (Zoom video communication or What's app application) (iii) standard care and in addition to a video call as described above using an explanatory short video on bowel preparation (video film), streamed to the patient's mobile device or computer.

Read the detailed description

Adequate bowel preparation is crucial for a successful and effective colonoscopy examination. Nevertheless, poor bowel preparation in patients is common and may lead to a lower quality of the examination that means a reduction in the rate of cecum intubation and lower detection rate of early and advanced adenoma. Finally, poor bowel preparation can lead to an abruption of the examination.

Digital advancement has been made in the context of colonoscopy bowel preparation, however high quality studies are still needed Ziv Medical Centre (ZMC) is a 300 bed governmental hospital located in Safed, Northern Israel that serves a diverse population. The gastroenterology department carries out approximately 1300 colonoscopies per year. A rapid audit has shown that approximately 15% of colonoscopies are stopped and up to 40% are incomplete, partly as a result of sub-optimal preparation.

The aim of this study is to determine whether better preparation by making full use of digital tools can increase patient compliance with the preparation methods for colonoscopy, and as a result improve bowel preparation quality and colonoscopy outcomes in a cost-effective manner.

This single blinded randomized controlled trial compares the effectiveness of bowel preparation in participants randomly assigned to one of three colonoscopy preparation groups (i) a written hand out containing all information required for bowel preparation (standard care) (ii) standard care and in addition a video call with a professional nurse conducted via digital devices and a free software (Zoom video communication or What's app application) (iii) standard care and in addition to a video call as described above using an explanatory short video on bowel preparation (video film), streamed to the patient's mobile device or computer.

All patients included in the trial will receive standard care 10 days before the examination. Patients randomized to the groups with a video call or a video call + video film will be contacted by a nurse to determine an appointment to the 10th day before examination. Patients randomized to the study arm including an educational video film will be sent a link to the video film after the video call. On the day of the exam, during the examination, the medical doctor records an OBPS score as described. After the exam, the medical doctor will register whether the exam was complete, incomplete, stopped and whether hospitalization was needed. After the examination and recovery, all patients will receive a short satisfaction questionnaire.

02

Conditions studied

  • Colonoscopy

Keywords

  • colonoscopy
  • gastroenterology
  • bowel preparation
  • digital
  • colorectal cancer screening
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In context

Lead sponsor

Ziv Hospital is the lead sponsor of 83 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • age >18 years
  • access to a digital device (smart phone, tablet, personal computer, laptop- this includes individuals who can use devices from household of relatives)
  • ability to understand instructions in Hebrew or Arabic
  • ability to sign a digital consent

Exclusion criteria

Exclusion Criteria:

  • pregnancy (first trimester)
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
825 participants (estimated)

Study arms

  • Active comparator
    Standard of care

    Standard of care includes a written paper sheet that summarizes information about the colonoscopy procedure and bowel preparation.

    Other: Standard of care

  • Experimental
    Standard of care + Video call

    The video call will be performed at a designated time with a GE educated nurse. The purpose of the video call is (i) to clarify the patient in person about the colonoscopy procedure (ii) efficiently prepare the patient for bowel preparation by; asking the patient about her/his medical condition, the indication for colonoscopy, medical history, current medical status and medications currently taken. The patient will be inquired, whether she/he went through colonoscopy in the past, what preparation methods were undertaken and what the outcome of the examination was. Based on the information collected during the conversation, the designated nurse performing the interview will tailor the method of bowel preparation for the patient in terms of kind of relaxant, adjustment of medication intake and dietary adjustments before the examination.

    Other: Standard of care + Video call

  • Experimental
    Standard of care + Video call + Educational video film

    The video film will explain the colonoscopy procedure and the bowel preparation procedure, in layman's terms and in the patient's preferred language (Hebrew or Arabic).

    Other: Standard of care + Video call + Educational video film

Interventions

  • OtherStandard of care

    A written hand out containing all information required for bowel preparation

  • OtherStandard of care + Video call

    Standard of care and in addition a video call with a professional nurse conducted via digital devices and a free software (Zoom video communication or What's app application)

  • OtherStandard of care + Video call + Educational video film

    Standard of care and in addition to a video call, an explanatory short video on bowel preparation (video film), streamed to the patient's mobile device or computer

06

What researchers measure

Primary outcomes

  1. The Ottawa Bowel Preparation Scale (OBPS)

    A standard method used to assess a patient's bowel preparation for colonoscopies. The bowel preparation score is a sum of a segmental score (right-colon, mid-colon and rectosigmoid-colon) and a fluid quantity score. The segmental score is quantified on a scale of 0 to 4, with; 0 indicating perfect cleansing, 1 indicating good cleansing, 2 indicating Fair cleansing, 3 indicating poor cleansing and 4 indicating inadequate cleansing. Overall fluid quantity is quantified on a scale of 0 to 2, with; 0 indicating no fluid in the colon and 2 indicating a large amount of fluid in the colon. Both the colon score and fluid score result in an overall score ranging from 0 to 14, with; 0 an Excellent cleansing quality and 14 indicates the worst cleansing quality. Estimations of the scores are made by the medical doctors during the exam and are fed into a commercial software that calculates the overall OBPS score.

    Time frame: OBPS will be evaluated during the colonoscopy procedure

Secondary outcomes

  1. Patient's satisfaction questionaire

    Patients will be asked about various aspects of the preparation using likert scales- the scores for each question will be compared across groups. The questionaires will include several questions about demographic background such as education level and occupation.

    Time frame: Questionnaires will be given to the patients immediately after the colonoscopy

  2. Colonoscopy completion

    The proportion of successfully completed colonoscopies will be quantified.

    Time frame: Colonoscopy completion will be recorded for 1 year

  3. The proportional change in the annual cost of treatment services

    The proportional change in the annual cost of running the service will be calculated, taking into account costs (research nurse, cost of developing the video etc.) and saving (averted complications, failed colonoscopies requiring re-booking etc.)

    Time frame: 1 year

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 17, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05734079
Lead sponsor
Ziv Hospital
Responsible party
Toni Ashqar (Dr. Toni Ashqar, Senior gastroenterologist, Ziv Hospital) — Principal investigator
First posted
Feb 17, 2023
Start date
Apr 1, 2023 (estimated)
Primary completion
Apr 1, 2024 (estimated)
Completion
Jul 1, 2024 (estimated)
Last update
Feb 17, 2023

Study contacts

Toni Ashqar, Dr.
Contact
toniashqar@gmail.com
+972528225103
Neta Tuvia, Dr.
Contact
netat@ziv.gov.il
+972-583971644
Toni Ashqar, Dr.
principal investigator · Ziv Medical Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is status unknown, as verified in Feb 2023. You cannot join it, but the record below documents what was studied.

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