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COPDNCT04370990

Automated Oxygen Administration -Rethinking Interventions Alleviating Dyspnea in Patients With COPD

A study testing O2matic in people with COPD and Hypoxia, run by Copenhagen University Hospital, Hvidovre at 5 sites in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Chronic Obstructive Pulmonary Disease (COPD) is associated with high morbidity and mortality. The Danish Lung Association estimates that 320,000 Danes live with COPD, of which approximately 50,000 with severe COPD. Read more about this study

Who is it for?
Ages 35 years and older
Conditions the study is for
COPD, Hypoxia, Closed-Loop Communication
What is being tested?
O2matic
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
157 participants
Where
5 sitesDenmark
Study dates
1 Sep 2019to 1 May 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 35 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • COPD veryfied by Forced Expiratory Volume in 1 sec (Fev1) divided by forced Vital Capacity (FVC)< 0,70
  • Admission due to exercabation in COPD
  • COPD exacerbation and pneumonia can be included
  • Expeted duration of admission >48 hours
  • Need for oxygen supplementation (SpO2<= 88% in room air) Cognitive able to participate in the study
  • Willing to participate and give informed consent

Who cannot join

  • Need or anticipated need for mechanical ventilation ( Intermittent continuous Positive Airway Pressure (CPAP) is allowed)
  • Major comorbidities causing hypoxemia (cancer, heart disease, pulmonary embolia)
  • Asthma or other respiratory conditions requiring higher SpO2 than normal for COPD Pregnancy
  • Cognitive barrierers for participation

Trial locations and contacts

5 sites in 1 country.

5 sites in 1 country

Denmark5 sites
  • Bispebjerg University Hospital

    Copenhagen, 2400

  • Hvidovre University Hospital

    Copenhagen, 2650

  • Herlev University Hospital

    Copenhagen, 2730

  • Gentofte University Hospital

    Copenhagen, 2900

  • Nordsjællands Hospital

    Frederikssund, 3600

Other trials in Denmark

About this study

Official title: Does Robot-administered Oxygen Have Effect on the Perception of Dyspnea in Patients Admitted With COPD and Hypoxemia?

Chronic Obstructive Pulmonary Disease (COPD) is associated with high morbidity and mortality. The Danish Lung Association estimates that 320,000 Danes live with COPD, of which approximately 50,000 with severe COPD. In 2017, records showed that 23,979 admissions in Denmark were related to COPD; of these patients, about 20% were readmitted 2-30 days after discharge. The main symptom is dyspnea, which is often accompanied by anxiety. Primary treatment is; oxygen, bronchiolitis, prednisolone, morfica, NIV, and anxiolytics.

Researchers at Hvidovre Hospital have developed an oxygen robot that continuously monitors the patient's SaO2 (oxygen saturation) and automatically administrates the oxygen depending on it. The preliminary results show that patients with robot-administrated oxygen were within defined SaO2 range in 85.7% of the time versus 46.6% when oxygen was nurse-administrated. The research was conducted as a multicentre Randomized Controlled Trial focusing on physiological end-points.

Read more

There is a lack of knowledge about the patient perspective of treatment with the oxygen robot.

The purpose of this study is:

  1. To examine the effect of robot-administered oxygen on patients' perception of dyspnoea, including the emotional response in the form of anxiety and depression

The perspective is to be able to provide a holistic response to whether robot-administered oxygen can be a better method of treating and alleviating dyspnoea.

Read the detailed description

Chronic Obstructive Pulmonary Disease (COPD) is a high prevalence disease and is associated with high morbidity and mortality worldwide. In 2017, there were 23.979 COPD related admissions in Denmark, approximately 10% died during hospitalization, while 20% of survivors were readmitted between day 2-30 after discharge.

Patients with COPD often experience long disease trajectories characterized by a substantial burden of symptoms, impaired functional status, multiple admissions and thereby reduced quality of life.

The cardinal symptom dyspnea is associated with hypoxemia, anxiety and depression. Evidence shows that depression is a significant risk factor for disabling dyspnea, while risk of anxiety increases with the severity of Dyspnea. The prevalence of anxiety and depression is indicated to lie between 10%-55% and 10%-86% in patients hospitalized with COPD in exacerbation . Patients with COPD have an 85% increased risk of developing anxiety compared to a matching control group without COPD. The prevalence of anxiety is 10 times higher among patients with COPD than in the background population and are strongly associated with the risk of hospitalization, long admissions, readmissions and death. Anxiety and depression are often treated with benzodiazepines which have a respiratory suppressive effect. Consumption of benzodiazepines increases disease progression, and studies have shown that 31.7% of patients with COPD have a benzodiazepine consumption and that 9% initiate a new benzodiazepine ordination in conjunction with an exacerbation.

The evidence that oxygen prevents disease progression and mortality is consistent, but there is a lack of knowledge about whether oxygen, can reduce the intensity of dyspnea in patients with COPD.

In the acute phase of an exacerbation the oxygen flow is titrated to achieve a SaO2 between 88-92%. Keeping patients with COPD within the given SaO2 range is essential because too low SaO2 can induce tissue damage, heart overload and difficulty concentrating, while hyperoxaemia can inhibit respiration and increase the risk of hypercapnia, acidosis and the need for ventilatory support in the form of Non-invasive Ventilation (NIV).

In clinical practice, oxygen flow is administered and titrated, via aggregates, by nurses based on point observations, with the risk of patients being outside optimal SaO2 range, between observations.

To improve practice, a group of researchers at Hvidovre Hospital has developed an oxygen robot, called O2matic, which continuously monitors the patient's SaO2 and automatically administrates oxygenflow according to it.

O2Matic has been tested in a randomized controlled trial in 2018. Patients admitted with an exacerbation of COPD and hypoxemia (SaO2 ≤ 88%) was included (N = 19). The design was crossover and patients were allocated to either 4 hours of manual oxygen administration via nurse followed by 4 hours of oxygen administration via O2Matic, or vice versa. The study showed that patients with O2matic controlled oxygen administration were within defined SaO2 range in 85.7% of the time versus 46,6% of the time when the oxygen was controlled and administrated by a nurse . These results are in consensus with a former Canadian study testing an alternative oxygen robot (FreeO2). The two RCT Studies provide evidence to investigate robot-administered oxygen therapy for inpatient patients with exacerbation of COPD in a larger multicenter RCT.

Dyspnea is defined as; "A subjective experience of breathing discomfort that consist of qualitatively distinct sensations that vary in intensity". The experience of dyspnea is a product of a physical perception based on signals from the body to the brain followed by the cognitive processing of these into an emotional experience. Dyspnea is thus an emotional and sensational experience based on perceptual afferent feedback from various respiratory receptors. Up to 16 possible mechanisms are involved in the process . Given the above, dyspnea is a complex symptom, mainly induced by the body's attempts to obtain homeostasis, when subjected to hypoxemia. Despite this dyspnea is not the same as hypoxemia, as it has not been clearly demonstrated that reduced hypoxemia, by oxygen therapy also reduces Dyspnea. However, there are indications in the literature that oxygen therapy can reduce the experience of dyspnea. A significant barrier to the use of oxygen therapy as an intervention on fragmentary dyspnea in patients with COPD is the risk of hypercapnia and acidosis. Oxygen therapy administrated according to saturation in a closed-loop-feedback-system by a robot, could potentially be an intervention to relieve fragmentary dyspnea in patients with COPD. International guidelines show that dyspnea is not treated consistently nor effectively in the advanced stages of the disease.

Opioids are one of the most widely used agents in the treatments of dyspnea. Opioids suppress' respiration and treatment should be balanced to avoid respiratory depression.

Guidelines points out the importance of identifying and graduate the intensity of dyspnea in clinical practice, without indicating any superior instruments to achieve this. Majority of instruments developed, describe dyspnea in relation to activity. As COPD progress, dyspnea intensifies and patients will become more inactive and often live a sedentary life.

Few questionnaires measure the sensory and emotional domains of dyspnea independently of activity and diagnose. One is the multidimensional Dyspnoea profile (MDP) that has currently been translated into Danish.

In order to reduce symptom burden, length of hospital stay, number of re-admissions and mortality, new knowledge and more effective methods for treating and alleviating dyspnea and the associated anxiety and depression are needed in patients with COPD.

Studies investigating the effect of oxygen therapy, including time with and degree of hypoxemia, in hypoxemic patients experiencing dyspnea, anxiety or depression during hospitalization with acute exacerbation, could not be identified.

Because O2matic provides a new and unique opportunity to reduce and illuminate time with hypoxemia during hospitalization and patient's subjective experience of the sensory and emotional aspects of dyspnea can be reported on a validated questionnaire via MDP, the investigators now have an option to investigate if a robot intervention, that reduces time with hypoxemia, has an effect on dyspnea in patients admitted with a exacerbation of COPD. Furthermore, investigators want to examine whether this intervention alters the consumption of opioids and benzodiazepines.

Primary hypothesis. Robot-administered oxygen reduces the perception of dyspnea measured at scale A1 on the multidimensional Dyspnea Profile (MDP), in patients with COPD and hypoxemia.

Primary objective. To investigate if oxygen administration by O2matic has an effect on the perception of dyspnea in patients admitted with an exacerbation of COPD and hypoxemia, versus conventional oxygen administration by oxygen aggregate and a nurse Primary end points.

  • Global dyspnea measured on scale A1 on multidimensional Dyspnea Profile (MDP) Secondary hypothesis. Oxygen administration by O2matic reduces the sensory and emotional dimension of dyspnea, respiratory symptoms, anxiety and depression, as well as consumption of anxiolytics in patients admitted with hypoxemia and exacerbation of COPD versus conventional Oxygen management by aggregate and nurse Secondary aim. To investigate if oxygen administration by O2matic has an effect on the sensory and emotional dimension of dyspnea, respiratory symptoms, anxiety and depression, as well as the consumption of anxiolytics in patients admitted with hypoxemia and exacerbation in COPD versus Conventional oxygen management by aggregate and nurse Secondary end-points.
  • Sensory and emotional dimension of dyspnea described by The Sensory Quality scale (SQ) and the A2 scale of the MDP
  • Current dyspnea measured on visual Analog scale (VAS)
  • Accumulated dyspnea over 3 days measured on VAS
  • Respiratory symptoms described by COPD Assessment Test
  • Anxiety described by HADS A score
  • Depression described by HADS D scores
  • Consumption of anxiolytics reported in Mg and in number of administrations

Following variables will be tested for confounding:

Age, gender, BMI, smoking status, package year, Long-term Oxygen Therapy (LOT), FEV1, GOLD classification A-D and Prednisolone reported in Mg

Being tested
O2matic
Keywords
O2matic, Multidimensional Dyspnea Profile
Medical subject headings
Pulmonary Disease, Chronic Obstructive, Hypoxia, Teach-Back Communication, Dyspnea, Anxiety Disorders, Depression

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • O2maticDevice

    O2matic is a closed-loop-system that controls oxygenadministration according to SpO2. The aim is to maintain SpO2 within a predefined target interval, E.G. 88-92% with the lowest possible supplementation of oxygen by nasal cannula

Study groups in NCT04370990
Study groupRoleWhat they receive
ActiveActive comparatorUsual care plus O2matic controlled oxygen therapy for a maximum of 3 days or until weaning from oxygen supplementation
Receives: Device: O2matic
controleNo interventionUsual care plus manual controlled oxygen therapy by nursing staff. O2matic used in monitoring mode to measure SpO2 continuously

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Global dyspnea measured on scale A1 on multidimensional Dyspnea Profile (MDP)

    Multidimensional Dyspnea Profile (MDP) is validated for patients with COPD (40) The schedule is an instrument consisting of 11 rating scales that describe both the sensory and emotional dimension of dyspnea in a user-specified focus period.Patients perception of unpleasantness or discomfort in breathing sensations described as global dyspnea measured on an intensity scale from 0 (anchored by term; neutral) -10(anchored by term; unbearable )

    Measured: 3 days

Secondary outcomes (4)
  1. The sensory dimension of dyspnea

    The SQ-scale of the Multidimensional Dyspnea Profile (MDP) Multidimensional Dyspnea Profile (MDP) is validated for patients with COPD. The schedule is an instrument consisting of 11 rating scales that describe both the sensory and emotional dimension of dyspnea in a user-specified focus period. The sensory dimension of dyspnea is described by 5 categorical variables. The intensity of the symptoms described by the variables is indicated by numerical scales from 0-10, called Sensory Questions (SQ) (range 0-50).

    Measured: 3 days

  2. The emotional dimension of dyspnea

    The A2-Scale of the Multidimensional Dyspnea Profile (MDP) Multidimensional Dyspnea Profile (MDP) is validated for patients with COPD. The schedule is an instrument consisting of 11 rating scales that describe both the sensory and emotional dimension of dyspnea in a user-specified focus period.The emotional dimension of dyspnea is also accessed with five variables measuring the intensity by numerical scales from 0-10, the scale is called the emotional response A2 (range 0-50).

    Measured: 3 days

  3. Current dyspnea

    Current dyspnea measured on a Visual analog scale (VASD). Sensation of dyspnea expressed in subject's feelings of breathlessness measured by Visual Analogue Scale for Dyspnea (VASD).

    Patients subjective sensation of dyspnea expressed as feelings of breathlessness is measured on a vertical line length equal to 100mm. VAS-scale consist of one construction and no subscales are provided.

    Each end of the line showing words that anchors the scale and describes the extreme e.g. "No breathlessness at all" or "Worst possible breathlessness" complimented by a describing smiley looking happy or sad, but no words describing intermediate positions (VAS-scale).

    Measured: 3 days

  4. Accumulated dyspnea

    accumulated dyspnea over past 3 days measured on Visual analog scale (VASD). Sensation of dyspnea expressed in subject's feelings of breathlessness measured by Visual Analogue Scale for Dyspnea (VASD).

    Patients subjective sensation of dyspnea expressed as feelings of breathlessness is measured on a vertical line length equal to 100mm. VAS-scale consist of one construction and no subscales are provided.

    Each end of the line showing words that anchors the scale and describes the extreme e.g. "No breathlessness at all" or "Worst possible breathlessness" complimented by a describing smiley looking happy or sad, but no words describing intermediate positions (VAS-scale).

    Measured: 3 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted1 May 2020
  2. Study start1 Sep 2019
  3. Primary completion1 May 2022
  4. Study completion1 May 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Open label randomized controlled parallel study
Masking
None (open label)
Enrolment
157 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04370990
Sponsor's protocol ID
Ethic committee H-17040114
Status last verified
Oct 2022
First submitted
28 Apr 2020
Last updated
26 Oct 2022
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing O2matic in people with COPD and Hypoxia, run by Copenhagen University Hospital, Hvidovre at 5 sites in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Oct 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Global dyspnea measured on scale A1 on multidimensional Dyspnea Profile (MDP) (time frame: 3 days). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Oct 2022.

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