NCT02031926

Brief Summary

Healthy subjects will be trained to used correctly a positive expiratory pressure device. The aim of the study is to evaluate te reproductibility of the correct used of the device after training

Trial Health

87
On Track

Trial Health Score

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

Enrollment
30

participants targeted

Target at P25-P50 for not_applicable healthy

Timeline
Completed

Started Nov 2012

Typical duration for not_applicable healthy

Geographic Reach
1 country

1 active site

Status
completed

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

November 1, 2012

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2012

Completed
1.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2014

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

January 7, 2014

Completed
2 days until next milestone

First Posted

Study publicly available on registry

January 9, 2014

Completed
Last Updated

January 9, 2014

Status Verified

January 1, 2014

Enrollment Period

Same day

First QC Date

January 7, 2014

Last Update Submit

January 8, 2014

Conditions

Healthy

Outcome Measures

Primary Outcomes (1)

  • Expiratory pressure

    within the 7 first days

Secondary Outcomes (1)

  • Succes rate

    Every day

Study Arms (1)

Positive expiratory pressure

EXPERIMENTAL
Device: Positive expiratory pressure

Interventions

Positive expiratory pressureDEVICE
Positive expiratory pressure

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • No lung disease
  • Older than 18 years

You may not qualify if:

  • Psychological disorder

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Cliniques universitaires Saint-Luc

Brussels, 1200, Belgium

Location

MeSH Terms

Interventions

Positive-Pressure Respiration

Intervention Hierarchy (Ancestors)

Respiration, ArtificialAirway ManagementTherapeuticsRespiratory Therapy

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Physiotherapist, PhD

Study Record Dates

First Submitted

January 7, 2014

First Posted

January 9, 2014

Study Start

November 1, 2012

Primary Completion

November 1, 2012

Study Completion

January 1, 2014

Last Updated

January 9, 2014

Record last verified: 2014-01

Locations

BE(1)