- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02140827
Instant Messaging Program (Wechat) Improve the Quality of Bowel Preparation
Communication Through Instant Messaging Program for the Improvement of Bowel Preparation: a Two Centers Study
Colonoscopy is the gold standard in the diagnosis of colorectal disease. The success of colonoscopy depends on high-quality bowel preparation by patients. Inadequate bowel cleansing reduces the cecal intubation rate, and the polyp detection rate (PDR). It also increases costs, mostly due to repeated procedures. The quality of bowel cleansing has remained suboptimal even though numerous different products and regimens have been tested and compared in no fewer than six meta-analyses. Therefore, a completely different approach to improve bowel cleansing is welcome.
Here the investigators assume that instant messaging program (Wechat) delivery the detail and FAQ (Frequently Asked Questions) of bowel preparation instructions would improve the quality of the bowel preparation. The Wechat program has some advantages, 1. Wechat supports over 400 million users, nearly half of the mobile subscribers population in China; 2. Wechat provided a real time communications including voice messages, pictures and text exchange timely; 3.Compare with telephone, Wechat is economical of both time and money; 4. Compare with bowel preparation instructional software and litera or cartoon educational booklet, Wechat is more interactive and responsive.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Guangdong
-
Foshan, Guangdong, China, 528000
- Department of gastroenterology, Chancheng Central Hospital of Foshan
-
-
Shaanxi
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Xi'an, Shaanxi, China, 710032
- Department of gastroenterology, Shaanxi Second People's Hospital
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Xi'an, Shaanxi, China, 710032
- Xijing Hospital of Digestive Diseases
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- age 18-80
- PEG as purgatives;
- using we-chat software by patients or their relatives
- outpatients
Exclusion Criteria:
- history of colorectal surgery
- known severe colonic stricture or obstructing tumor
- known or suspected bowel obstruction or perforation
- pregnant or lactating women
- patients who cannot give informed consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: IMP education
patients in this group are educated about bowel preparation by instant messaging program and meanwhile a booklet was also sent to them.
|
The detail and FAQ (Frequently Asked Questions) of bowel preparation instructions is delivered by Wechat.
Other Names:
|
|
No Intervention: normal education
patients in this group are educated about bowel preparation on the day of reservation by nurse for about 15 minutes and meanwhile a booklet was also sent to them.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Adequate bowel preparation quality at the time of colonoscopy defined by Ottawa score<6
Time Frame: up to 5 months
|
Ottawa score:A)cleanliness of each part of the colon: 0=excellent 1=good 2=fair 3=poor 4=inadequate B)fluid in whole colon: small=0 moderate=1 large=2 The bowel preparation was considered inadequate if (1) inadequate visualization on colonoscopy defined by Ottawa score≥6; (2) the colonoscopy was cancelled because of poor bowel preparation; (3) incompleted colonoscopy because of inadequate bowel preparation (the Ottawa score was rated as 14 when patients with failed colonoscopy because of inadequate bowel preparation). |
up to 5 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Polyp detection rate
Time Frame: up to 5 months
|
The proportion of participants with at least one polyp in each group
|
up to 5 months
|
|
Compliance rate to instruction
Time Frame: up to 5 months
|
The proportion of participants compliance to the instructions of diet and bowel preparation in each group
|
up to 5 months
|
|
Willingness undergo a repeated bowel preparation
Time Frame: up to 5 months
|
The number of participants have a willingness to undergo a repeated bowel preparation if needed
|
up to 5 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Yanglin Pan, M.D., Air Force Military Medical University, China
- Principal Investigator: Limei Wang, M.D., Department of gastroenterology, Shaanxi Second People's Hospital
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 20140508-5 (Other Identifier: Ethics committee of Xijing Hospital)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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