Educational Programme in Diaphragm Ultrasonographic Assessment

April 18, 2019 updated by: Paolo Navalesi

Evaluation of a 2-hour Educational Programme in Diaphragm Ultrasonographic Assessment

Diaphragm ultrasound non-invasively explores the diaphragm function and it can be useful in several clinical situations. Diaphragm ultrasound is able to evaluate the cranio-caudal displacement of the diaphragm and its thickening fraction at the end of inspiration, in relation to the end-expiratory value.

While several studies have been conducted in the evaluation of educational programmes for echocardiography, to date data lack regarding this aspect in diaphragm ultrasonographic assessment.

Based on the experience gained in some specialization schools in Anaesthesia and Intensive Care, the investigators hypothesize that the participation in a two-hour course, including a theoretical part and a practical training, allows to acquire the appropriate theoretical and practical skills necessary to correctly perform the measurement of the diaphragm excursion and thickening fraction, compared to the theoretical lesson only, followed by a brief explanation by an expert tutor, on the practical use of the ultrasound.

The investigators hypothesized that the association of the theoretical part and of the practical training is able to obtain:

  1. Passing the theoretical test with at least 70% of the correct answers;
  2. The correct identification of the areas where the probe is affixed;
  3. The appropriate measure of Diaphragmatic thickening and displacement.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

  1. INTRODUCTION Diaphragm ultrasound non-invasively explores the diaphragm function and it can be useful in several clinical situations. Diaphragm ultrasound is able to evaluate the cranio-caudal displacement of the diaphragm and its thickening fraction at the end of inspiration, in relation to the end-expiratory value. These parameters provide useful data in the evaluation and management of patients affected by diaphragm dysfunction; moreover, they are gaining an increasing role in the evaluation of patients undergoing mechanical ventilation.

    To assess the diaphragm activity, clinicians use two different sonographic windows:

    i. to evaluate diaphragmatic thickness in the zone of apposition of the diaphragm to the rib cage. Physicians can assess thickening fraction between the 8th and 10th intercostal space, on the anterior or midaxillary line, 0.5-2 cm below the costophfrenic angle. The zone of apposition is the area of the chest wall where the abdominal contents reach the lower rib cage. In this area, the diaphragm is observed as a structure made of three distinct layers: a non-echogenic central layer bordered by two echogenic layers, the peritoneum and the diaphragmatic pleurae. To obtain adequate images of diaphragmatic thickness in M mode and 2D mode, a linear high-frequency probe (≥10 MHz) is necessary. The diaphragmatic thickness can be measured during quiet spontaneous breathing and during a maximal inspiratory and expiratory effort. An index of diaphragmatic thickening, the thickening fraction (TF) can be calculated using the M mode (TF = thickness at endinspiration - thickness at end-expiration/thickness at end-expiration). Diaphragmatic thickening fraction can be used as an index of diaphragmatic efficiency as a pressure generator. In normal individuals, there is a wide range of tdi at functional residual capacity (FRC), ranging between 1.8 to 3 mm. As lung volume increases from the residual volume (RV) to total lung capacity (TLC) there is a mean tdi increase of 54 % (range 42-78 %). Furthermore, the diaphragm also thickens during a maximal inspiratory pressure (Pimax) maneuver at FRC. A thickening ratio of 2.6 can be measured, dividing the diaphragmatic thickness during Pimax at FRC by the diaphragmatic thickness while relaxing at FRC.

    ii. the physicians can also assess the diaphragmatic displacement (or excursion) trough a 3.5-5 mHz phased array probe. The probe is placed immediately below the right costal margin in the mid-clavicular line or in the right anterior axillary line, and it is directed medially, cephalad and dorsally, in order that the ultrasound beam perpendicularly reached the hemi-diaphragm in its posterior third portion. After obtaining the best approach in two-dimensional mode, the displacement was measured in M-mode displaying the motion of the hemi-diaphragm along the selected line. In healthy subjects during spontaneous breathing, the inspiratory diaphragm excursion is 1.34 ± 0.18 cm.

    In patients undergoing assist mechanical ventilation, the thickening fraction is an indicator of inspiratory effort. While several studies have been conducted in the evaluation of educational programmes for echocardiography, to date data regarding this aspect in diaphragm ultrasonographic assessment lack.

  2. AIM OF THE STUDY

Based on the experience gained in some specialization schools in Anesthesia and Intensive Care, the investigators hypothesize that the participation in a two-hour course, including a theoretical part and a practical training, allows to acquire the appropriate theoretical and practical skills necessary to correctly perform the measurement of the diaphragm excursion and thickening fraction, compared to the theoretical lesson only, followed by a brief explanation by an expert tutor, on the practical use of the ultrasound. The investigators hypothesized that the association of the theoretical part and of the practical training is able to obtain:

  1. Passing the theoretical test with at least 70% of the correct answers;
  2. The correct identification of the areas where the probe is affixed;
  3. The appropriate measure of diaphragmatic TF and displacement.

3. MATERIALS AND METHODS Participants will be randomized into two groups similar for age and gender. First of all, a theoretical part will be conducted through the administration of a video-tutorial to both groups, aimed to teach of ultrasonographic basic principles, of sonographic windows and of the anatomical reference points for the diaphragmatic ultrasonography. At the end of the video, a 10-point questionnaire will be administered to evaluate the level of learning for each participant.

Every single participant will pass the test if he/she correctly answers to at least the 70% of the questions. Those passing the test will be randomized to two groups. Participants will be randomly assigned to one of the two groups using opaque, sealed, numbered envelopes. The investigators will use a computer-generated randomization sequence, generated by an independent biostatistician who is not otherwise involved in the trial. The envelopes will be kept in head of nurses offices in every institution's critical care unit. The researcher will distribute the envelopes to participants, which will independently open it. Participants will communicate the random group allocation to the researcher who will assign the participant to the study group.

The first group will access the practical training, during which each participant will be followed by a tutor who will interactively explain, using a healthy volunteer, how to perform the ultrasound scan of the diaphragm. The ultrasound will be performed on a healthy volunteer first by the tutor and then by the participants. During the exercise, the tutor himself will supervise each individual learner.

The second group will directly perform the ultrasound examination of the diaphragm. The expert tutor will only show the learners how to use the various functions of the ultrasound, the linear and convex probes both in two-dimensional and in M-mode.

The tutors assigned to both groups will have proven experience in thoracic ultrasound. In order to standardize the practical teaching of the technique, the tutors will meet telematically by agreeing the modalities of the training and / or administration of the basics on the use of the ultrasound.

To evaluate the learning, each participant of both groups will perform the ultrasound scan of the diaphragm in both acoustic windows and acquire the images on the healthy volunteer. The tutor will verify the correctness of the acquired images and make the measurements.

A classroom helper will record the measurements taken and make the scanned image available again for a new measurement. Therefore, on the same image, the participant, who will not know the measurements performed by the tutor, will perform his own measurement, the results of which will be recorded by the person in charge of the classroom. This procedure will be carried out both for the measurement of the excursion and for that of the thickening fraction.

If the participant fails to correctly display the diaphragm in one of the two windows, the result will be negative. Those who will identify the diaphragm in both windows will be admitted to the next step and will be able to measure the diaphragmatic displacement and the diaphragmatic thickening fraction. The result will be considered positive if the learner will obtain measurement values for thickening fraction that deviate from those performed by the expert tutor at most 20% and diaphragmatic displacement values that deviate from the values obtained by the tutor to a maximum of +/- 2 mm.

A. Study design Multicenter randomized controlled study.

B. Population 58 students for each of the two groups, for a total of 116 volunteers, enrolled between medical and surgical students, health professions, specializing in medical-surgical disciplines who have no experience in the field of ultrasound and are divided into two groups, of which one will receive both the theoretical lesson and the practical training, while the other at the end of the theoretical lesson will receive only general notions about the practical use of the ultrasound.

C. Statistical analysis Based on the above considerations, at the end of the course, a difference is expected between groups receiving the practical training compared and control, in terms of achievement of the outcome equal to at least 30%.

Study Type

Interventional

Enrollment (Actual)

172

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • CZ
      • Catanzaro, CZ, Italy, 88100
        • Eugenio Garofalo

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • 116 students with no experience in the field of ultrasound

Exclusion Criteria:

  • None

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: "Tutor" group

After a theoretical part through the administration of a video-tutorial, a 10-point questionnaire will be administered to evaluate the level of learning for each participant. Every single participant will pass the test if he/she correctly answer to >70% of the questions. Those passing the test, will be randomized to two groups.

The interventional group will access the practical training, during which each participant will be followed by a tutor who will interactively explain, using a healthy volunteer, how to perform the ultrasound scan of the diaphragm. The ultrasound will be performed on a healthy volunteer first by the tutor and then by the participants. During the exercise, each individual learner will be supervised by the tutor himself.

The participants will access the practical training, during which each participant will be followed by a tutor who will interactively explain, using a healthy volunteer, how to perform the ultrasound scan of the diaphragm. The ultrasound will be performed on a healthy volunteer first by the tutor and then by the participants. During the exercise, each individual learner will be supervised by the tutor himself.
No Intervention: "No tutor" group
This control group will directly perform the ultrasound examination of the diaphragm. The expert tutor will only show the learners how to use the various functions of the ultrasound, the linear and convex probes both in two-dimensional and in M-mode.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ultrasonographic skills - Thickening Fraction
Time Frame: Soon after the video-tutorial (within 30 minutes), when participants perform diaphragm ultrasound
Measurement of thickening fraction. If measurements will deviate from those recorded by the expert within the 20% of the value, the result will be considered positive
Soon after the video-tutorial (within 30 minutes), when participants perform diaphragm ultrasound
Ultrasonographic skills - Diaphragm Displacement
Time Frame: Soon after the video-tutorial (within 30 minutes), when participants perform diaphragm ultrasound
Measurement of Diaphragm Displacement. If students' measurements will deviate from those recorded by the expert within the +/- 2 mm, the result will be considered positive.
Soon after the video-tutorial (within 30 minutes), when participants perform diaphragm ultrasound

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2018

Primary Completion (Actual)

February 28, 2019

Study Completion (Actual)

February 28, 2019

Study Registration Dates

First Submitted

July 16, 2018

First Submitted That Met QC Criteria

October 9, 2018

First Posted (Actual)

October 12, 2018

Study Record Updates

Last Update Posted (Actual)

April 22, 2019

Last Update Submitted That Met QC Criteria

April 18, 2019

Last Verified

April 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • US Diaphragm Learning

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

All individual, de-identified participant data will be shared after motivated request by e-mailing.

IPD Sharing Time Frame

From the anticipated end of the trial

IPD Sharing Access Criteria

Motivated request by e-mailing

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • ANALYTIC_CODE
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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