Effect of the Automatic Surveillance System on Surveillance Rate of Colorectal Postpolypectomy Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: AI based automatic surveillance (AS) system (ENDOANGEL-AS) reminds the patients through by telephone ., AI based automatic surveillance (AS) system (ENDOANGEL-AS) reminds the patients through message., Manually remind the patients.
- Who it may be relevant to
- Registry conditions: Artificial Intelligence, Surveillance. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
In this study, we proposed a prospective study about the effect of the automatic surveillance system on surveillance rate of colorectal postpolypectomy patients. The enrolled patients were divided into group A with intelligent surveillance system reminding though telephone and message, group B with intelligent surveillance system reminding though message, group C with manual reminder, and group D with natural state. The surveillance among the four groups were compared.
Detailed description
The adherence of doctors to published colorectal post-polypectomy surveillance guidelines varies greatly, and patient follow-up is critical but time-consuming. Previous studies we developed an automatic surveillance (AS) system to accurately identify post-polypectomy patients, assign surveillance intervals for different risks of patients and proactively follow up with patients in time. In this study, we proposed a prospective study about the effect of the automatic surveillance system on surveillance rate of colorectal postpolypectomy patients. The enrolled patients were divided into group A with intelligent surveillance system reminding though telephone and message, group B with intelligent surveillance system reminding though message, group C with manual reminder, and group D with natural state. The surveillance among the four groups were compared.
Interventions
- Other AI based automatic surveillance (AS) system (ENDOANGEL-AS) reminds the patients through by telephone .
An automatic surveillance (AS) system to accurately identify post-polypectomy patients, assign surveillance intervals for different risks of patients and proactively follow up with patients at certain times. AI based automatic surveillance (AS) system (ENDOANGEL-AS) reminds patients by telephone. - Other AI based automatic surveillance (AS) system (ENDOANGEL-AS) reminds the patients through message.
An automatic surveillance (AS) system to accurately identify post-polypectomy patients, assign surveillance intervals for different risks of patients and proactively follow up with patients at certain times. AI based automatic surveillance (AS) system (ENDOANGEL-AS) reminds patients through message. - Other Manually remind the patients
Medical staff remind patients manually .
Primary outcome measures
- On-time Surveillance Rate [Time frame: From enrollment to study completion, assessed up to 3 years.]
Secondary outcome measures (11)
- Surveillance Rate [Time frame: From enrollment to study completion, assessed up to 3 years.]
- Advance Surveillance Rate [Time frame: From enrollment to study completion, assessed up to 3 years.]
- Delayed Surveillance Rate [Time frame: From enrollment to study completion, assessed up to 3 years.]
- The accuracy of identifing post-polypectomy patients [Time frame: 1 day At the time of enrollment]
- The accuracy of classifying risk levels [Time frame: 1 day At the time of enrollment]
- The accuracy of assigning surveillance intervals [Time frame: 1 day At the time of enrollment]
- lesion progression rate [Time frame: From enrollment to study completion, assessed up to 3 years.]
- lesion persistence rate [Time frame: From enrollment to study completion, assessed up to 3 years.]
- lesion regression rate [Time frame: From enrollment to study completion, assessed up to 3 years.]
- The incidence rate of early colorectal cancer [Time frame: From enrollment to study completion, assessed up to 3 years.]
- The incidence rate of colorectal cancer [Time frame: From enrollment to study completion, assessed up to 3 years.]
Eligibility criteria
Inclusion criteria
- Male or female aged 18 years or older who undergo colonoscopy.
Exclusion criteria
- 1)No pathological result.
- 2\) No or invalid contact information.
- 3\) The surveillance interval cannot be determined according to the surveillance guidelines, including poor bowel preparation, colorectal cancer or suspicious malignance, surgery or colorectal ESD history, those who fail to complete colonoscopy due to unbearable, pathological indications of not polyps, hamartoma or lymphoma polyps, history of ulcerative colitis, and so on.
- 4\) Has participated in other clinical trials, signed the informed consent form and is in the surveillance period of other clinical trials.
- 5\) Have drug or alcohol abuse or psychological disorder in the past five years.
- 6）Pregnancy.
- 7）Not suitable for recruitment after investigator evaluation because of other high-risk conditions.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Screening
Study locations
China · 1 center
- Renmin Hospital of Wuhan University — Wuhan
Identifiers
NCT: NCT05894850 · EA-19-003-29