CClinicalTrials.gg
Status unknownNCT04204031MONOXUpdated Dec 18, 2019

Objective Evaluation of the Number of Use Hour of Oxygen Therapy in Patients Receiving Supplemental Oxygen

An interventional study of Presentation of the adherence record in Chronic Respiratory Failure With Hypoxia and Chronic Obstructive Pulmonary Disease, sponsored by Haute Ecole de Santé Vaud. Status unknown at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2019-12-18.

Sponsored by Haute Ecole de Santé Vaud · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Dec 2019), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study is to measure the actual use time in patients receiving supplemental oxygen using a new easy-to-use electronic remote monitoring device (TeleOx™)

Read the detailed description

The first phase of the study is observational. Oxygen use time of patients with chronic respiratory failure under long term oxygen therapy will be objectively measured using a electronic remote monitoring device (TeleOx™) over 15 days. The actual use time will be compared to their oxygen prescription.

Participants whose actual time of use will be less than prescribed will be offered an intervention which will consist of a presentation of the adherence record. The participant will also be asked about the presence of possible barriers concerning the use of oxygen therapy. The collaborator in charge of home visits will attempt to resolve these barriers as much as possible. Only participants with an actual time of use less than prescribed will be offered this intervention and will continue the monitoring over a period of 15 additional days.

02

Conditions studied

  • Chronic Respiratory Failure With Hypoxia
  • Chronic Obstructive Pulmonary Disease

Keywords

  • Long term oxygen therapy
  • adherence
  • electronic monitoring
03

In context

Lung Diseases, Obstructive

2,592 studies on the registry are indexed under Lung Diseases, Obstructive; 198 are open to participants now.

This study's planned enrollment of 60 is close to the median of 66 across 1,837 interventional studies indexed under Lung Diseases, Obstructive.

Browse Lung Diseases, Obstructive studies →

Lead sponsor

Haute Ecole de Santé Vaud is the lead sponsor of 17 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Long term oxygeno-therapy patients in stable condition without pulmonary exacerbation in the month before inclusion
  • Oxygen prescription for at least 15 hours/day

Exclusion criteria

Exclusion Criteria:

  • under 18 years old
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Other
    Presentation of the adherence record

    Following a first observation period of 15 days, participants whose actual time of use will be less than prescribed will be offered an intervention which will consist of a presentation of the adherence record. The participant will also be asked about the presence of possible barriers concerning the use of oxygen therapy. The collaborator in charge of home visits will attempt to resolve these barriers as much as possible. Only participants with an actual time of use less than prescribed will be offered this intervention and will continue the monitoring over a period of 15 additional days.

    Behavioral: Presentation of the adherence record

Interventions

  • BehavioralPresentation of the adherence record

    Adherence record will be presented to participants with an actual time of use less than prescribed. The participant will also be asked about the presence of possible barriers concerning the use of oxygen therapy. The collaborator in charge of home visits will attempt to resolve these barriers as much as possible.

06

What researchers measure

Primary outcomes

  1. Oxygen use time

    Average oxygen use time (hours/day) measured with a TeleOx device

    Time frame: 15 days

07

Study locations

1 site
  • Haute Ecole de Santé Vaud (HESAV)
    Lausanne, 1011, Switzerland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 18, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04204031
Lead sponsor
Haute Ecole de Santé Vaud
Collaborators
University Hospital, Geneva, Ligue Pulmonaire Genevoise
Responsible party
Olivier Contal (Ordinary Professor HES, Haute Ecole de Santé Vaud) — Principal investigator
First posted
Dec 18, 2019
Start date
Jan 2, 2020 (estimated)
Primary completion
Sep 30, 2020 (estimated)
Completion
Sep 30, 2020 (estimated)
Last update
Dec 18, 2019

Study contacts

Olivier Contal, PhD
Contact
olivier.contal@hesav.ch
+41213168122
Olivier Contal, PhD
principal investigator · Haute Ecole de Santé Vaud

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2019. You cannot join it, but the record below documents what was studied.

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