Image

Procedural Skills Transfer in Bronchoscopy

Procedural Skills Transfer in Bronchoscopy

Recruiting
16 years and older
All
Phase N/A

Powered by AI

Overview

Brief summary The goal of this Feasibility study is to capture bronchoscopy data from patients (Group1) and bronchoscopists (Group 2) over a period of three years. The investigators wish to collect the pre-procedure CT scans and endoscopy videos of 300 patients. Up to 20 bronchoscopists will take part in the study

Primary outcomes

  1. To collect imaging data from patients undergoing routine bronchoscopy procedures
  2. To collect movement data from clinicians performing the routine bronchoscopy procedures using a sensory Glove

Secondary outcomes

  1. Integrate the data gathered with procedure guidelines to develop a representation of procedure success using machine learning algorithms.
  2. Develop an actionable knowledge base for bronchoscopy skill transfer to novice/untrained medical staff.
  3. Investigate the feasibility of developing models of bronchoscopy procedures to develop training tools in the future

There are no additional samples or time commitments from the participants in Group 1.

The participants in Group 2 will be asked to answer a short questionnaire about their experience in performing bronchoscopies and will be asked to wear a sensory glove during the bronchoscopy procedure to capture their hand movements.

Description

Bronchoscopy is a procedure for visualising the inside of the lung and airways. During bronchoscopy, a thin tube is passed through the patient's mouth or nose, down the throat and into the lungs. This allows the practitioner to examine the patient's airways for abnormalities such as inflammation. Additionally, samples may be taken from inside the lungs.

Success rate of bronchoscopy relies on the practitioners experience. Patients undergoing bronchoscopy performed by novice bronchoscopists have an increased complication rate. Data from clinical practice suggest that bronchoscopy has a prolonged learning curve and trainees should perform a number of procedures, under supervision, to learn the technique.

In this study the investigators aim to capture bronchoscopy data from patients (Group1) and bronchoscopists (Group 2) over a period of 3 years. The investigators will collect the pre-procedure CT scans and endoscopy videos of 300 patients. Up to 20 bronchoscopists will take part in the study by answering a short questionnaire on their experience and wearing sensorized gloves which will record their hand movements during the procedure. the investigators aim to use this data to develop computer algorithms and simulators that will assist in the training of new bronchoscopists, decreasing the time required to learn the technique and improving patient safety.

Eligibility

Inclusion Criteria Group 1

  • over 16 years of age
  • patients identified as requiring a bronchoscopy by their clinician
  • patients must have had a CT scan in the 8 weeks prior to the procedure
  • capacity to consent

Exclusion Criteria Group 1 - Patients who have not had a CT scan in the 8 weeks prior to the procedure

Inclusion Criteria Group 2

  • Suitably qualified bronchoscopists, this may include trainee bronchoscopists

Exclusion Criteria Group 2

  • Clinicians who do not give consent to participate in the study
  • Clinicians who are not comfortable performing bronchoscopy while wearing the lightweight glove

Study details
    Respiratory Disease

NCT07168408

University of Edinburgh

15 October 2025

Step 1 Get in touch with the nearest study center
We have submitted the contact information you provided to the research team at {{SITE_NAME}}. A copy of the message has been sent to your email for your records.
Would you like to be notified about other trials? Sign up for Patient Notification Services.
Sign up

Send a message

Enter your contact details to connect with study team

Investigator Avatar

Primary Contact

  Other languages supported:

First name*
Last name*
Email*
Phone number*
Other language

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.