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The Role of Ambulatory Oxygen in Improving the Effectiveness of Pulmonary Rehabilitation for COPD Patients

The Role of Ambulatory Oxygen in Improving the Effectiveness of Pulmonary Rehabilitation for Chronic Obstructive Pulmonary Diseases Patients

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02707770
Enrollment
20
Registered
2016-03-14
Start date
2016-04-14
Completion date
2017-12-30
Last updated
2021-03-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Diseases

Keywords

COPD, pulmonary rehabilitation, ambulatory oxygen therapy

Brief summary

Pulmonary rehabilitation (PR) is an exercise program tailored for patients with chronic lung disease that is a core part of the management of patients with Chronic Obstructive Pulmonary Disease (COPD). Many COPD patients develop low oxygen levels (desaturation) during exercise and this is often discovered when they are being evaluated for PR. Current practice is to administer oxygen to COPD patients with exercise-induced desaturation, but this is based on very limited evidence. This limited evidence relates to a short-term increase in exercise capacity and it is not known if this translates into longer term increases in activity or whether providing these patients with oxygen improves outcomes after PR. In addition it is not known if patients given ambulatory oxygen continue to use it after completing PR. Evidence for a beneficial effect of oxygen would provide a more solid evidence base for its use. Conversely demonstration of no effect would allow reassessment of the use of oxygen and whether the costs are justified. Therefore the aims of this study are to assess the effects of oxygen on outcomes from PR and assess the usage of ambulatory oxygen following completion of PR.

Detailed description

The study will be a randomised, single-blinded study comparing oxygen with air in Chronic Obstructive Pulmonary Disease (COPD) patients undergoing Pulmonary Rehabilitation (PR). The study subjects will be patients with a confirmed diagnosis of COPD who have been accepted for PR and who are not hypoxemic at rest, but have exercise-induced desaturation (defined as a fall in oxygen saturations (SaO2) ≥4% to at least \<90%, or any fall to a SaO2 \<90%) and demonstrate positive improvement with use of ambulatory oxygen as per the British Thoracic Society 2015 Oxygen guidelines. It is standard practice for patients to have this assessment prior to commencing PR and as part of the assessment the flow rate required to increase the SaO2 to ≥90% during exercise will be determined. Patients will be recruited from PR programs at imperial college health care trust hospitals. The subjects will be randomised to receive either oxygen at the flow rate determined at the initial assessment to a maximum flow rate of 6 litres per minute, or room air. The subjects will then undergo a standard program of PR over 6 - 8 weeks and then undergo reassessment. 20 patients are required in each group to detect a 30% effect size on the 6 minute walk test (6MWT) with 80% power at the 5% significance level and 29 patients in each group to detect a 25% effect with 80% power. Therefore a minimum of 20 patients per group will be included. Baseline assessments prior to commencing PR will include symptom and quality of life assessments including Borg scale for assessment of breathlessness, Chronic Respiratory Questionnaire (CRQ), COPD Assessment Tool (CAT) and the Hospital Anxiety and Depression score (HAD). A 6 minute walk test (6MWT) will be carried out as this is a widely used and well validated tool to measure exercise capacity. A handheld dynamometer will be used to obtain more detailed measures of quadriceps muscle strength. In addition we will measure activity at home during and after PR using pedometers as this has never been investigated previously.These are simple devices that can be attached to patients and count the numbers of steps during a day and therefore provide an estimate of activity in the home environment. A yamax Digi-walker SW-200 pedometer will be used to count the number of steps taken per day. Patients will be instructed to wear the device on left side of the body all the time, except when sleeping or showering. Pedometer placement was standardised by placing it on the belt or waistband, in the midline of the thigh, consistent with the manufacturers recommendation and with other studies conducted previously. Patients will be record daily step counts on daily diary cards until their final follow up. The measures of exercise capacity at the follow up assessment will be carried out off oxygen and will be carried out by an observer blinded as to whether they received oxygen or not during PR. All patients will be provided with ambulatory oxygen for domiciliary use after completing PR. The hypothesis is that use of oxygen in selected patients improves exercise capacity during PR. The measurable aims will be exercise capacity and on-going usage of oxygen in this patient group. Primary Objective Assess the effects of ambulatory oxygen on outcomes from Pulmonary Rehabilitation Secondary Objectives 1. Assess the proportion of patients that wish to continue to use ambulatory oxygen. 2. Assess the usage of ambulatory oxygen following completion of Pulmonary Rehabilitation 3. Assess whether initiation of ambulatory oxygen before or after PR has any influence on adherence to usage at 8 and 12 weeks.

Interventions

OTHERPulmonary Rehabilitation

Sponsors

National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
Imperial College Healthcare NHS Trust
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. A confirmed diagnosis of Chronic Obstructive Pulmonary Disease (COPD) 2. Fulfil the clinical criteria for Pulmonary Rehabilitation (PR) 3. Demonstrate exercise-induced desaturation (defined as a fall in SaO2 ≥4% to at least \<90%, or any fall to a SaO2 \<90%) and demonstrate positive improvement with use of ambulatory oxygen as per the British Thoracic Society 2015 Oxygen Guidelines

Exclusion criteria

1. Use of long term oxygen therapy 2. Unable to provide informed consent 3. Significant respiratory disease other than COPD 4. Any patient needing more than 6 litres per minute oxygen to correct desaturation 5. Severe desaturation: SaO2 \< 80% during 6 Minute Walk Test 6. Any absolute contraindication to Pulmonary Rehabilitation

Design outcomes

Primary

MeasureTime frameDescription
Change in Functional Exercise Capacity0, 8weeks6 Minute Walk Test (6MWT)- Distance in meters

Secondary

MeasureTime frameDescription
Number of Participants Reporting a Change in the Quality of Life0,8weeksChronic Respiratory Questionnaire(CRQ)- Number of Participants achieving minimal clinically important difference (MCID) in CRQ compared between baseline and follow up assessment.
Number of Participants Reporting a Change in Anxiety Score0,8weeksHospital anxiety and depression score- Anxiety component (HADS-A)-Numbers of participants achieving Minimal clinically important difference in HADS-A compared between baseline and follow up assessment.
Number of Participants Reporting Change in Depression Score0,8weeksHospital anxiety and depression score- Depression component (HADS-D)-Numbers of participants achieving Minimal clinically important difference in HADS-D compared between baseline and follow up assessment.
Number of Participants Reporting Change in Chronic Obstructive Pulmonary Diseases Assessment Test (CAT)0,8weeksChronic Obstructive Pulmonary diseases Assessment Test (CAT score)-Numbers of participants achieving Minimal clinically important difference in CAT score compared between baseline and follow up assessment.
Number of Patients Reporting Change in Physical Activity8 weeksPedometer- Number of step counts
Number of Participants With Change in Quadriceps Muscle Strength0,8 weeksHandheld Muscle testing- Number of participants achieving Minimal clinical important difference in quadriceps muscle strength compared between baseline and follow up assessment

Countries

United Kingdom

Participant flow

Participants by arm

ArmCount
Ambulatory Oxygen
Patient will use ambulatory oxygen during pulmonary rehabilitation programme (flow rate determined at the initial assessment to a maximum flow rate of 6 litres per minute)
9
Room Air
Patient will breath on room air during pulmonary rehabilitation programme
10
Total19

Baseline characteristics

CharacteristicRoom AirTotalAmbulatory Oxygen
Age, Continuous72 years72.5 years73 years
Race and Ethnicity Not Collected0 Participants
Region of Enrollment
United Kingdom
10 participants19 participants9 participants
Sex: Female, Male
Female
6 Participants8 Participants2 Participants
Sex: Female, Male
Male
4 Participants11 Participants7 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 90 / 10
other
Total, other adverse events
0 / 90 / 10
serious
Total, serious adverse events
0 / 90 / 10

Outcome results

Primary

Change in Functional Exercise Capacity

6 Minute Walk Test (6MWT)- Distance in meters

Time frame: 0, 8weeks

ArmMeasureGroupValue (MEAN)
Ambulatory OxygenChange in Functional Exercise CapacityBaseline -0332 meters
Ambulatory OxygenChange in Functional Exercise CapacityPost PR - 8weeks346 meters
Room AirChange in Functional Exercise CapacityBaseline -0335 meters
Room AirChange in Functional Exercise CapacityPost PR - 8weeks340 meters
Secondary

Number of Participants Reporting a Change in Anxiety Score

Hospital anxiety and depression score- Anxiety component (HADS-A)-Numbers of participants achieving Minimal clinically important difference in HADS-A compared between baseline and follow up assessment.

Time frame: 0,8weeks

ArmMeasureValue (NUMBER)
Ambulatory OxygenNumber of Participants Reporting a Change in Anxiety Score4 participants
Room AirNumber of Participants Reporting a Change in Anxiety Score3 participants
Secondary

Number of Participants Reporting a Change in the Quality of Life

Chronic Respiratory Questionnaire(CRQ)- Number of Participants achieving minimal clinically important difference (MCID) in CRQ compared between baseline and follow up assessment.

Time frame: 0,8weeks

ArmMeasureValue (NUMBER)
Ambulatory OxygenNumber of Participants Reporting a Change in the Quality of Life3 participants
Room AirNumber of Participants Reporting a Change in the Quality of Life2 participants
Secondary

Number of Participants Reporting Change in Chronic Obstructive Pulmonary Diseases Assessment Test (CAT)

Chronic Obstructive Pulmonary diseases Assessment Test (CAT score)-Numbers of participants achieving Minimal clinically important difference in CAT score compared between baseline and follow up assessment.

Time frame: 0,8weeks

ArmMeasureValue (NUMBER)
Ambulatory OxygenNumber of Participants Reporting Change in Chronic Obstructive Pulmonary Diseases Assessment Test (CAT)5 participants
Room AirNumber of Participants Reporting Change in Chronic Obstructive Pulmonary Diseases Assessment Test (CAT)3 participants
Secondary

Number of Participants Reporting Change in Depression Score

Hospital anxiety and depression score- Depression component (HADS-D)-Numbers of participants achieving Minimal clinically important difference in HADS-D compared between baseline and follow up assessment.

Time frame: 0,8weeks

ArmMeasureValue (NUMBER)
Ambulatory OxygenNumber of Participants Reporting Change in Depression Score2 participants
Room AirNumber of Participants Reporting Change in Depression Score2 participants
Secondary

Number of Participants With Change in Quadriceps Muscle Strength

Handheld Muscle testing- Number of participants achieving Minimal clinical important difference in quadriceps muscle strength compared between baseline and follow up assessment

Time frame: 0,8 weeks

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Ambulatory OxygenNumber of Participants With Change in Quadriceps Muscle Strength0 Participants
Room AirNumber of Participants With Change in Quadriceps Muscle Strength0 Participants
Secondary

Number of Patients Reporting Change in Physical Activity

Pedometer- Number of step counts

Time frame: 8 weeks

Population: Due to technical problems identified with accuracy of device, this outcome measure was excluded from study

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026