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

Primary Purpose

Chronic Obstructive Pulmonary Diseases

Status
Terminated
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Pulmonary Rehabilitation
Sponsored by
Imperial College Healthcare NHS Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Diseases focused on measuring COPD, pulmonary rehabilitation, ambulatory oxygen therapy

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • St Marys Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Ambulatory oxygen

Room air

Arm Description

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)

Patient will breath on room air during pulmonary rehabilitation programme

Outcomes

Primary Outcome Measures

Change in Functional Exercise Capacity
6 Minute Walk Test (6MWT)- Distance in meters

Secondary Outcome Measures

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.
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.
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.
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.
Number of Patients Reporting Change in Physical Activity
Pedometer- Number of step counts
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

Full Information

First Posted
February 23, 2016
Last Updated
March 3, 2021
Sponsor
Imperial College Healthcare NHS Trust
Collaborators
National Institute for Health Research, United Kingdom
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1. Study Identification

Unique Protocol Identification Number
NCT02707770
Brief Title
The Role of Ambulatory Oxygen in Improving the Effectiveness of Pulmonary Rehabilitation for COPD Patients
Official Title
The Role of Ambulatory Oxygen in Improving the Effectiveness of Pulmonary Rehabilitation for Chronic Obstructive Pulmonary Diseases Patients
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Terminated
Why Stopped
Funding for the study finished before anticipated participants enrolled
Study Start Date
April 14, 2016 (Actual)
Primary Completion Date
June 19, 2017 (Actual)
Study Completion Date
December 30, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College Healthcare NHS Trust
Collaborators
National Institute for Health Research, United Kingdom

4. Oversight

Data Monitoring Committee
No

5. Study Description

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 Assess the proportion of patients that wish to continue to use ambulatory oxygen. Assess the usage of ambulatory oxygen following completion of Pulmonary Rehabilitation Assess whether initiation of ambulatory oxygen before or after PR has any influence on adherence to usage at 8 and 12 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Diseases
Keywords
COPD, pulmonary rehabilitation, ambulatory oxygen therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ambulatory oxygen
Arm Type
Experimental
Arm Description
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)
Arm Title
Room air
Arm Type
Placebo Comparator
Arm Description
Patient will breath on room air during pulmonary rehabilitation programme
Intervention Type
Other
Intervention Name(s)
Pulmonary Rehabilitation
Primary Outcome Measure Information:
Title
Change in Functional Exercise Capacity
Description
6 Minute Walk Test (6MWT)- Distance in meters
Time Frame
0, 8weeks
Secondary Outcome Measure Information:
Title
Number of Participants Reporting a Change in the Quality of Life
Description
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
Title
Number of Participants Reporting a Change in Anxiety Score
Description
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
Title
Number of Participants Reporting Change in Depression Score
Description
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
Title
Number of Participants Reporting Change in Chronic Obstructive Pulmonary Diseases Assessment Test (CAT)
Description
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
Title
Number of Patients Reporting Change in Physical Activity
Description
Pedometer- Number of step counts
Time Frame
8 weeks
Title
Number of Participants With Change in Quadriceps Muscle Strength
Description
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

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A confirmed diagnosis of Chronic Obstructive Pulmonary Disease (COPD) Fulfil the clinical criteria for Pulmonary Rehabilitation (PR) 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: Use of long term oxygen therapy Unable to provide informed consent Significant respiratory disease other than COPD Any patient needing more than 6 litres per minute oxygen to correct desaturation Severe desaturation: SaO2 < 80% during 6 Minute Walk Test Any absolute contraindication to Pulmonary Rehabilitation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vijayaragavan Padmanaban, MPT
Organizational Affiliation
Imperial healthcare NHS Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
St Marys Hospital
City
London
ZIP/Postal Code
W2 21NY
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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

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