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Impact of Digital Communication Assist Tools in Endoscopic Team Communication During COVID-19

Impact of Digital Enhanced Telecommunication for Team Communication in Endoscopic Procedures During COVID-19 Pandemic

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04680858
Acronym
EndoCom
Enrollment
500
Registered
2020-12-23
Start date
2020-07-01
Completion date
2021-02-15
Last updated
2020-12-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Endoscopy, Communication

Keywords

endoscopy, team communication, endoscopic procedure, COVID-19

Brief summary

Team work is highly challenged by the COVID-19 pandemic. Necessary protective equipment as FFP-mask and face shields impair communication significantly.Objective of the study is to evalaute the impact of digital enhanced telecommunication in endoscopic procedures.

Detailed description

Optimal communication is crucial for team work in high class endoscopy. Team work is highly challenged by the COVID-19 pandemic. Necessary protective equipment as FFP-mask and face shields impair communication significantly. Digital enhanced approaches to maintain team communication during endoscopic procedures are mandatory not only in actual circumstances. Materials and methods:A prospective, two-armed interventional study will be performed at an endoscopy unit at a tertiary center. 200 endoscopic examinations (EGD, colonoscopy, EUS, ERCP) were randomly assigned (1:1) to a group that was performed with DECT equipped endoscopy team or with standard communication. All examinations were performed under protective equipment. Primary outcome was rate of communication associated adverse events. Secondary outcomes included team subjectively perceived comfort with DECT enhanced communication during endoscopic work, duration of examinations, SAE.

Interventions

OTHERDECT

Use of a digital enhanced telecommunication headset for team communication

Sponsors

University of Ulm
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Two-armed study

Eligibility

Sex/Gender
ALL
Age
18 Years to 68 Years
Healthy volunteers
No

Inclusion criteria

* Member of staff of the endoscopic team (Doctor, nurse)

Exclusion criteria

* Deafness * significantly impaired hearing

Design outcomes

Primary

MeasureTime frameDescription
Communication associated adverse eventsFrom start to stop of endoscopic procedureAdverse events arising from impaired communication by COVID-19 protection equipment

Secondary

MeasureTime frameDescription
Severe adverse eventsFrom start to stop of endoscopic procedureSevere adverse evatent, not arising from from impaired communication by COVID-19 protection equipment
Subjective Comfort of DECT communicationFrom start to stop of endoscopic procedureSubjectiveley perceived level of comfort using DECT communication during endoscopic procedures rated by numeric rating scale (1-6)
Endoscopic timeFrom start to stop of endoscopic procedureDuration of performed endoscopic procedures

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026