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Fibrotic Interstitial Lung DiseasePhase 2NCT06053164

Ambulatory Oxygen Therapy for Individuals With Mild-to-moderate Interstitial Lung Disease

A Phase 2 study testing Exertional Oxygen and Education and Support in people with Fibrotic Interstitial Lung Disease, run by University of Alberta at 1 site in Canada.

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Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
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Trial summary

The investigators plan to conduct a study to find out if giving portable oxygen therapy (during physical activity) to patients with interstitial lung disease will improve quality of life, exercise tolerance, shortness of breath, and blood vessel function. Oxygen will be provided for a period of 8 weeks. Read more about this study

Who is it for?
Ages 18 to 85 years
Conditions the study is for
Fibrotic Interstitial Lung Disease
What is being tested?
Exertional Oxygen and Education and Support
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteCanada
Study dates
1 Jul 2025to 1 Mar 2027
Phase
Phase 2

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 18 to 85 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Individuals with fibrotic ILD (all sub-groups of ILD) who have normal oxygen saturation at rest (SpO2 > 90%) but develop exertional hypoxemia as demonstrated by a SpO2 = 80-89% with activity (measured during 6MWT).

Who cannot join

  • Use of home oxygen therapy within the previous year for the management of ILD, co-morbid conditions that may require oxygen therapy (such as COPD, cardiovascular disease, or other illnesses), or individuals that require the use of non-invasive ventilation. Additionally, individuals with significant cardiovascular, metabolic, neuromuscular or any other disease that could contribute to dyspnea or abnormal cardiopulmonary responses to exercise will be excluded. Individuals with musculoskeletal injuries that prevent them from completing cycle ergometry exercise trials and ambulation will also be excluded. Individuals with peripheral vascular disease will be excluded from measurement of vascular function (flow mediated dilation).

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Matt Rieger, PhD contact

7804928027

mrieger@ualberta.ca

Desi Fuhr, MSc contact

780.492.1121

fuhr@ualberta.ca

Canada1 site, 1 recruiting
  • Clinical Physiology Laboratory

    Edmonton, Alberta, T6G2R3

    Desi Fuhr, MSc, 780-492-1121, fuhr@ualberta.ca

    Michael K Stickland, PhD, 780-492-3995, michael.stickland@ualberta.ca

    Recruiting

Other trials in Canada

About this study

The investigators plan to conduct a study to find out if giving portable oxygen therapy (during physical activity) to patients with interstitial lung disease will improve quality of life, exercise tolerance, shortness of breath, and blood vessel function. Oxygen will be provided for a period of 8 weeks. Additionally, the investigators plan to investigate if it is helpful to deliver individualized support when providing oxygen therapy, through check-in phone calls with a respiratory therapist and by providing additional educational material.

Read the detailed description

Brief Summary:

The investigators plan to conduct a study to find out if giving portable oxygen therapy (during physical activity) to patients with interstitial lung disease will improve quality of life, exercise tolerance, shortness of breath, and blood vessel function. Oxygen will be provided for a period of 8 weeks. Additionally, the investigators plan to investigate if it is helpful to deliver individualized support when providing oxygen therapy, through check-in phone calls with a respiratory therapist and by providing additional educational material.

Detailed Description:

BACKGROUND

Interstitial lung disease (ILD) is comprised of a group of pulmonary diseases that are characterized by inflammation and/or lung parenchymal fibrosis. Individuals with ILD may be normoxic at rest; however, underlying impairments in gas exchange can contribute to a reduction in oxygen saturation (SpO2) during exertion. Hypoxemia can cause inflammation and cardiovascular dysfunction, which could lead to cardiac events. A recent study found that 78% of ILD patients had cardiovascular comorbidity, which was predictive of death within this ILD cohort.

Oxygen therapy is used in patients with advanced lung disease with resting hypoxemia; however, there is limited evidence regarding its clinical efficacy. Furthermore, there is little support to describe the benefit of ambulatory oxygen therapy in individuals with lung disease who are normoxemic at rest but become hypoxemic with exertion. Accordingly, thresholds for the prescription of oxygen therapy vary between (and within) health districts and geographical regions, and individuals who might benefit from supplemental oxygen typically do not qualify for funding of oxygen therapy under unclear guidelines. Furthermore, data from studies in patients with chronic obstructive pulmonary disease (COPD) are often extrapolated for use in guiding oxygen therapy in patients with ILD, which is likely inappropriate considering recent research demonstrated that individuals with fibrotic ILD experience greater hypoxemia than those with COPD during the 6-minute walk test (6MWT).

Oxygen therapy may be beneficial in reducing inflammation, oxidative stress, and pulmonary artery pressure, all of which are elevated in ILD. Furthermore, a reduction in dyspnea during exercise with exertional oxygen therapy might increase daily physical activity, exercise tolerance, and reduce overall sedentary time, which would have a positive effect on vascular function. These postulated outcomes, however, are confounded by various practical, psychological, and social challenges associated with use of an oxygen concentrator, as well as challenges with proper titration of oxygen levels (accurately targeting appropriate SpO2) in relation to exertional intensity. Paradoxically, if the flow of oxygen is too high, activation of inflammatory and oxidative pathways may inhibit the benefits related to the alleviation of hypoxemia. Thus, integration of patient-specific disease support tools is essential when initiating oxygen therapy to ensure appropriate oxygenation during exertion.

OBJECTIVE To assess the feasibility of oxygen therapy, education, and support for individuals with fibrotic interstitial lung disease and exertional hypoxemia. As a secondary objective, the effects of exertional oxygen therapy and support on physical activity, vascular function, and health-related quality of life in individuals with fibrotic interstitial lung disease will be investigated.

PRIMARY AND SECONDARY ENDPOINTS

Health related quality of life as assessed by the EQ-5D-5L and the K-BILD Exercise tolerance, assessed by 6MWD while breathing room air Daily physical activity and sedentary time as assessed by a remote monitor. Dyspnea, as measured by the Dyspnea 12 questionnaire Cough using the visual analog scale (VAS) and cough score (measured by Leicester Cough Questionnaire; LCQ) Vascular function, measured by flow mediated dilation (FMD) of the brachial artery Pulmonary artery systolic pressure (PASP) measured by cardiac echocardiography Cardiac systolic and diastolic function assessed by cardiac echocardiography Systemic inflammation

STUDY DESIGN

Single-blind (assessment team) open-label randomized control

TRIAL TREATMENT

Participants will be randomized into one of three arms:

Control:

(Arm 1) 8 Weeks of usual care (n=20)

Treatment:

(Arm 2) 8 Weeks of supplemental oxygen(n=20)

(Arm 3) 8 Weeks of supplemental oxygen plus educational materials and scheduled support (n=20)

All: 2-week baseline prior to intervention and 2-week washout post-intervention to document carry-over effect of intervention.

DURATION

Seven sessions will be completed over a 13-week period.

TIMELINE

Visit 1) Participant enrollment, medical history, standard pulmonary function test (PFT) and 6-minute walk test (6MWT); followed by 1-week for collection of baseline physical activity and SpO2. During this visit, participants will be provided a wrist-worn activity monitor and a finger-worn pulse oximeter. This visit will take approximately 3 hours.

Visit 2) Doppler measurements of systemic vascular function (flow mediated dilation) will be measured at rest while breathing room air. A small sample of venous blood will be taken to analyze inflammatory levels and reactive oxygen species. Participants will fill out questionnaires relating to health-related quality of life, dyspnea, and cough. Finally, participants will perform tests of lung diffusing capacity for carbon monoxide (DLCO) under three different conditions: seated, supine, and during exercise at 40W on a cycle ergometer.

Visit 3) One to three days after Visit 2, participants will return for the second day of pre-intervention baseline testing. An echocardiographic exam will be completed to determine pulmonary artery systolic pressure as well as systolic and diastolic function in the left and right ventricles of the heart. To enhance the Doppler signal during the cardiac ultrasound, agitated saline contrast will be used. Two 6-minute walk tests will then be completed, separated by half an hour. This visit will take approximately 2 hours. Following this day, participants will be randomized into one of three arms for an 8-week intervention.

Eight-week intervention, randomized into one of:

  • No oxygen
  • Exertional oxygen
  • Exertional oxygen + additional support

Visit 4) Repeat Day 2 protocol. Visit 5) Repeat Day 3 protocol.

Two-week washout period

Visit 6) Repeat Day 2 protocol. Visit 7) Repeat Day 3 protocol.

The total duration of time spent for each participant will be approximately 12 hours.

Being tested
Exertional Oxygen, Education and Support
Keywords
Exertional Oxygen, Ambulatory Oxygen, Interstitial Lung Disease
Medical subject headings
Lung Diseases, Interstitial

What participants receive

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

  • Exertional OxygenDrug

    Also called Supplemental oxygen, ambulatory oxygen

    Use of a portable oxygen concentrator for exertional activities lasting >2 minutes

  • Education and SupportBehavioural

    Participants will receive disease-specific educational material (Living Well with Pulmonary Fibrosis: Oxygen), and will have scheduled phone appointments with a certified respiratory educator after 1, 3, and 5 weeks of oxygen therapy in order to address individual barriers to oxygen use and facilitate the optimal use of portable oxygen.

Study groups in NCT06053164
Study groupRoleWhat they receive
Arm 1 - Usual CareNo intervention8 weeks of usual care with no supplemental oxygen provided
Arm 2 - Exertional OxygenExperimental8 weeks of portable oxygen use (from a concentrator) during exertion
Receives: Drug: Exertional Oxygen
Arm 3 - Exertional Oxygen + SupportExperimental8 weeks of portable oxygen use (from a concentrator) during exertion, plus additional phone calls with a respiratory educator and educational material
Receives: Drug: Exertional Oxygen; Behavioral: Education and Support

What is being measured

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

  1. Feasibility of investigation

    Number of patients recruited and completing the protocol in each arm

    Measured: 2 years

  2. Exercise tolerance

    6 minute walk distance

    Measured: Before and immediately after the intervention

  3. Health Related Quality of Life, (EuroQol-5 Dimension-5 Level; EQ-5D-5L)

    Questionnaire for Health-Related Quality of Life. Possible Range = 5-25; 5 = 11111 (no problems on any dimension); 25 = 55555 (extreme problems on all dimensions)

    Measured: Before and immediately after the intervention

  4. Health Related Quality of Life, (King's Brief Interstitial Lung Disease Questionnaire; KBILD)

    Health status questionnaire. Domain and total score ranges are 0-100; 100 represents best health status

    Measured: Before and immediately after the intervention

Secondary outcomes (6)
  1. Dyspnea (Dyspnea-12 Questionnaire)

    Range from 0-36, 0 represents no breathlessness and 36 represents maximal severity

    Measured: Before and immediately after the intervention

  2. Vascular function

    Flow-mediated dilation

    Measured: Before and immediately after the intervention

  3. Cough (Leicester cough questionnaire; LCQ)

    Quality of life measure of chronic cough. Range from 3-21, lower score indicating greater impairment of health status due to chronic cough

    Measured: Before and immediately after the intervention

  4. Pulmonary Artery Pressure

    Echocardiography-derived pulmonary artery systolic pressure

    Measured: Before and immediately after the intervention

  5. Cardiac Output

    Assessed by echocardiography (L/min)

    Measured: Before and immediately after the intervention

  6. Systemic Inflammation

    C-Reactive Protein (CRP, venous blood, mg/L)

    Measured: Before and immediately after the intervention

Timeline

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

  1. First posted25 Sep 2023
  2. Study start1 Jul 2025
  3. Primary completion1 Mar 2027 (estimated)
  4. Study completion1 Mar 2027 (estimated)

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 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Single-blind open-label randomized control
Masking
Double blind
Who is masked
Investigator, Outcomes assessor
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06053164
Sponsor's protocol ID
Pro00128503
Status last verified
Oct 2026
First submitted
3 Aug 2023
Last updated
23 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Khor YH, Holland AE, Goh NSL, Miller BR, Vlahos R, Bozinovski S, Lahham A, Glaspole I, McDonald CF. Ambulatory Oxygen in Fibrotic Interstitial Lung Disease: A Pilot, Randomized, Triple-Blinded, Sham-Controlled Trial. Chest. 2020 Jul;158(1):234-244. doi: 10.1016/j.chest.2020.01.049. Epub 2020 Feb 28.

    PubMed 32113924
  • Johannson KA, Pendharkar SR, Mathison K, Fell CD, Guenette JA, Kalluri M, Kolb M, Ryerson CJ. Supplemental Oxygen in Interstitial Lung Disease: An Art in Need of Science. Ann Am Thorac Soc. 2017 Sep;14(9):1373-1377. doi: 10.1513/AnnalsATS.201702-137OI.

    PubMed 28644693
  • Visca D, Mori L, Tsipouri V, Fleming S, Firouzi A, Bonini M, Pavitt MJ, Alfieri V, Canu S, Bonifazi M, Boccabella C, De Lauretis A, Stock CJW, Saunders P, Montgomery A, Hogben C, Stockford A, Pittet M, Brown J, Chua F, George PM, Molyneaux PL, Margaritopoulos GA, Kokosi M, Kouranos V, Russell AM, Birring SS, Chetta A, Maher TM, Cullinan P, Hopkinson NS, Banya W, Whitty JA, Adamali H, Spencer LG, Farquhar M, Sestini P, Wells AU, Renzoni EA. Effect of ambulatory oxygen on quality of life for patients with fibrotic lung disease (AmbOx): a prospective, open-label, mixed-method, crossover randomised controlled trial. Lancet Respir Med. 2018 Oct;6(10):759-770. doi: 10.1016/S2213-2600(18)30289-3. Epub 2018 Aug 28.

    PubMed 30170904

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