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The Effect of Routine Video-recording on Colonoscopy Quality Indicators.

M

Maria Sklodowska-Curie National Research Institute of Oncology

Status

Completed

Conditions

Colorectal Cancer

Treatments

Procedure: Implementation of routine videorecording
Behavioral: No routine videorecording

Study type

Interventional

Funder types

Other

Identifiers

NCT02054923
REC-QUALY

Details and patient eligibility

About

Routine video recording of the colonoscopy examination has been proposed as a simple and easy to implement method that could improve the quality of colonoscopy. The purpose of this study is to investigate whether implementation of routine video recording of screening colonoscopy withdrawal is effective as a means of supporting quality performance of colonoscopy. The study will be performed in 8 screening centers within the framework of a national colonoscopy screening program in Poland (the Polish Colonoscopy Screening Platform; PCSP). Individuals aged 55-64 years are eligible to participate in the PCSP. In the run-in period colonoscopy quality measures will be monitored through a dedicated joint database. Then eligible screening centres will be randomly assigned in a 1:1 ratio to the video recording group or the control group. Screening centres assigned to the video recording group will receive videorecorders and DVDs and will be asked to video record all screening colonoscopies (only withdrawal). Control group will be allowed to record colonoscopies on demand only. Then , the colonoscopy quality measures will again be monitored through a dedicated joint database. All the recorded DVDs will be reviewed to verify ceacal intubation and withdrawal time by the PCSP team.

Enrollment

5,200 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Screening centres participating in the Polish Colonoscopy Screening Platform (PCSP) between 2012 and 2013, in which no routine video recording of screening colonoscopies is performed
  • Screening centres which will sign informed consent

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

5,200 participants in 2 patient groups

Routine video recording group
Experimental group
Description:
Intervention: Procedure: Implementation of routine videorecording of colonoscopy withdrawal
Treatment:
Procedure: Implementation of routine videorecording
Control group
Active Comparator group
Description:
Intervention: Behavioral: No routine videorecording (on demand videorecording possible)
Treatment:
Behavioral: No routine videorecording

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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