NCT02703285

Brief Summary

The study aims to validate the interpretation of breath sounds by medical personnel

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2016

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2016

Completed
21 days until next milestone

First Submitted

Initial submission to the registry

February 22, 2016

Completed
8 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2016

Completed
8 days until next milestone

First Posted

Study publicly available on registry

March 9, 2016

Completed
Last Updated

March 14, 2016

Status Verified

March 1, 2016

Enrollment Period

29 days

First QC Date

February 22, 2016

Last Update Submit

March 11, 2016

Conditions

Respiration, Artificial

Outcome Measures

Primary Outcomes (1)

  • breathing sounds measured by questionnaire

    study participants selective listening to breath sounds, must mark in questionnaire what is the type of sound. 8 questions.

    1 day

Study Arms (1)

questionnaire

EXPERIMENTAL

task of the participants in the study to determine the chest sound based on specific sounds

Other: Sound

Interventions

SoundOTHER

task of the participants in the study to determine the chest sound based on specific sounds: Vesicular - Diminished; Expiratory Wheeze; Bronchovesicular; pneumonia; pulmonary Oedema; Stridor; Agonal respiration

questionnaire

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • give voluntary consent to participate in the study
  • paramedics, nurses, physicians

You may not qualify if:

  • not meet the above criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Medical University of Warsaw, Department of Emergency Medicine

Warsaw, Masovia, 02-005, Poland

RECRUITING

MeSH Terms

Conditions

Respiratory Aspiration

Interventions

Sound

Condition Hierarchy (Ancestors)

Respiration DisordersRespiratory Tract DiseasesPathologic ProcessesPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Radiation, NonionizingRadiationPhysical Phenomena

Study Officials

  • Lukasz Szarpak, PhD

    Medical University of Warsaw

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Lukasz Szarpak, PhD

CONTACT

+48500186225lukasz.szarpak@gmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lukasz Szarpak

Study Record Dates

First Submitted

February 22, 2016

First Posted

March 9, 2016

Study Start

February 1, 2016

Primary Completion

March 1, 2016

Study Completion

March 1, 2016

Last Updated

March 14, 2016

Record last verified: 2016-03

Locations

PL(1)