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CompletedNCT01584817Updated Dec 3, 2013

A Repeated Instruction by Telephone on the Day Before Colonoscopy to Patients Undergoing Colonoscopy

An interventional study of telephone education in Ottawa Score and Adenoma, sponsored by Air Force Military Medical University, China. Completed at 1 site in China. Open to participants aged 18 Years to 75 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-12-03.

Sponsored by Air Force Military Medical University, China · Not applicable, Interventional, and Screening

Phase
Not applicable
Study type
Interventional
Enrollment
605
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

Cell phone retell the instruction of bowel preparation on the day before colonoscopy would help patient to prepare for colonoscopy and improve the quality of the bowel preparation.

Read the detailed description

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 speed, the cecal intubation rate, and the number of polyps detected. 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 precolonoscopy bowel cleansing is welcome.

There are many factors effect the bowel preparation such as age, cirrhosis diabetes, drug compliance, cerebral infarction, dementia, history of major surgery. 20% of patients with poor bowel preparation were due to bad compliance. Studies found that addressing patient perceptions with an inexpensive and simple booklet based on the Health Belief Model improved preparation quality. We assume that doctor retelling the instruction of bowel preparation by cell phone on the day before colonoscopy would help patient to prepare for colonoscopy and improve the quality of the bowel preparation.

02

Conditions studied

  • Ottawa Score
  • Adenoma

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Keywords

  • colonoscopy
  • bowel preparation
  • education
03

In context

Adenoma

657 studies on the registry are indexed under Adenoma; 98 are open to participants now.

This study's enrollment of 605 is above the median of 250 across 412 interventional studies indexed under Adenoma.

Browse Adenoma studies →

Lead sponsor

Air Force Military Medical University, China is the lead sponsor of 172 studies on the registry; 36 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • patients undergoing colonoscopy

Exclusion criteria

Exclusion Criteria:

  • disturbance of water and electrolyte
  • history of colorectal surgery
  • severe colonic stricture or obstructing tumor
  • known or suspected bowel obstruction or perforation
  • toxic colitis or megacolon
  • dysphagia
  • compromised swallowing reflex or mental status
  • significant gastroparesis or gastric outlet obstruction or ileus
  • severe chronic renal failure (creatinine clearance \<30 mL/minute)
  • severe congestive heart failure (New York Heart Association class III or IV)
  • uncontrolled hypertension (average systolic blood pressure >170 mm Hg, average diastolic blood pressure >100 mm Hg)
  • pregnant or lactating women
  • patients who cannot give informed consent
05

Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
605 participants (actual)

Study arms

  • No intervention
    normal education

    patients in this arm was educated about bowel preparation on the day of reservation by nurse for 15 minutes and meanwhile a booklet was also sent to them.

  • Other
    telephone education

    A repeated instruction by telephone on the day before colonoscopy was conducted

    Other: telephone education

Interventions

  • Othertelephone education

    A repeated instruction by telephone on the day before colonoscopy was conducted

06

What researchers measure

Primary outcomes

  1. Adequate bowel preparation quality at the time of colonoscopy defined by Ottawa score<6

    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 or personal reasons; (3) incomplete colonoscopy.

    Time frame: up to 3 months

Secondary outcomes

  1. Cecum intubation time

    Total time of colonoscope intubation from anus to cecum

    Time frame: up to 3 months

  2. Withdrawal time

    Total time of colonoscope intubation from cecum to anus

    Time frame: up to 3 months

  3. Polyp detection rate

    The proportion of participants with at least one polyp in each group

    Time frame: up to 3 months

  4. Compliance rate to instruction

    The proportion of participants compliance to instruction of bowel preparation

    Time frame: up to 3 months

  5. Willingness undergo a repeated bowel preparation

    The number of patients have a willingness to undergo a repeated bowel preparation if needed

    Time frame: up to 3 months

07

Study locations

1 site
  • Endoscopic center, Xijing Hospital of Digestive Diseases
    Xi'an, Shaanxi 710032, China
08

References and documents

Publications

  • Liu X, Luo H, Zhang L, Leung FW, Liu Z, Wang X, Huang R, Hui N, Wu K, Fan D, Pan Y, Guo X. Telephone-based re-education on the day before colonoscopy improves the quality of bowel preparation and the polyp detection rate: a prospective, colonoscopist-blinded, randomised, controlled study. Gut. 2014 Jan;63(1):125-30. doi: 10.1136/gutjnl-2012-304292. Epub 2013 Mar 16. PubMed 23503044 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 3, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01584817
Lead sponsor
Air Force Military Medical University, China
Responsible party
Yanglin Pan (Associated professor, Air Force Military Medical University, China) — Principal investigator
First posted
Apr 25, 2012
Start date
Feb 2012
Primary completion
Jul 2012
Completion
Jul 2012
Last update
Dec 3, 2013

Study contacts

pan yanglin, MD.
principal investigator · Air Force Military Medical University, China

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2013. You cannot join it, but the record below documents what was studied.

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