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The Alfred Step Test Exercise Protocol (A-STEP), for Adults With Cystic Fibrosis. (A-STEP)

Primary Purpose

Cystic Fibrosis, Fibrosis, Lung Diseases

Status
Recruiting
Phase
Not Applicable
Locations
Australia
Study Type
Interventional
Intervention
A-STEP
A-STEP (New Protocol)
Comparator: CPET cycle ergometer (Gold Standard)
Sponsored by
The Alfred
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Cystic Fibrosis focused on measuring Exercise Testing, Maximal Exercise Testing, Maximal Exercise Capacity, Peak Exercise Capacity, Adults, Step Tests

Eligibility Criteria

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

INCLUSION

  • Confirmed Diagnosis of CF (by genotype or positive sweat test)
  • Aged 18yrs and older
  • FEV1 ≥20% (Forced expiration in 1 sec)
  • Stable baseline state. (Stable baseline state is defined as: clinically stable respiratory status, for at least 30 days, characterized by the absence of hospitalization and no changes in maintenance therapy during this period (Yankaskas et al 2004)).

EXCLUSION

  • Febrile
  • Haemoptysis
  • Uncontrolled asthma
  • Pneumothorax
  • Cardiac issues
  • Unreliable readings on pulse oximetry
  • Pulmonary hypertension
  • Unstable CF related diabetes (CFRD)
  • Vascular issues
  • Renal disease
  • Pregnancy
  • Body mass index (BMI) <18.0
  • Significant musculoskeletal issues
  • Unable to safely follow instructions

(ATS/ACCP 2003; Hebestreit 2015)

Sites / Locations

  • The Alfred HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

A-STEP

A-STEP (New Protocol)

CPET cycle ergometer (Gold Standard)

Arm Description

Study A) A-STEP Study Development of new exercise test protocol and Observational Feasibility/Safety Study (no comparator).

Study B) A-STEPmax Study Validity Study (random allocation of test order).

Study B) A-STEPmax Study Validity Study (random allocation of test order).

Outcomes

Primary Outcome Measures

Study B) Maximum oxygen uptake (VO2max)
The highest oxygen uptake achieved during the exercise test taken from inspired gas in a given period of time. Body weight is used to calculate this from oxygen consumption during the test. VO2peak may be used as a surrogate if VO2max is not achieved. Criteria for reaching maximum effort is not included in this document.
Study A) Oxygen Saturation
Standard objective outcome measures of field exercise testing. Measured via pulse oximetry.
Study A) Heart Rate
Standard objective outcome measures of field exercise testing. Measured via pulse oximetry.

Secondary Outcome Measures

Study B) Carbon Dioxide Production
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis with portable metabolic measurement equipment.
Study B) Respiratory Exchange Ratio
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis. The ratio of carbon dioxide production to oxygen consumption.
Study B) Minute Ventilation
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis. The product of tidal volume and respiratory rate.
Study B) Oxygen Pulse
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis. Calculated by dividing the oxygen consumption by heart rate.
Study B) Tidal Volume
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis. The volume of each breath taken.
Study B) Oxygen Saturation
Standard objective outcome measures of exercise testing. Measured via pulse oximetry.
Study B) Heart rate
Standard objective outcome measures of exercise testing. Measured via pulse oximetry.
Study B) Measures from Electrocardiogram
Used to monitor the patient's cardiac rhythm (CPET only)
Study A & B) Breathlessness and Leg Fatigue
Standard subjective outcome measures of exercise testing. Modified Borg 0-10.
Study A & B) Blood pressure
Standard outcome measure of exercise testing.
Study A & B) Duration of test; Highest level (mins and sec)/stage achieved; Reason for test termination.
Parameters of exercise test.

Full Information

First Posted
March 10, 2016
Last Updated
July 25, 2023
Sponsor
The Alfred
Collaborators
Monash University
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1. Study Identification

Unique Protocol Identification Number
NCT02717650
Brief Title
The Alfred Step Test Exercise Protocol (A-STEP), for Adults With Cystic Fibrosis.
Acronym
A-STEP
Official Title
Development; Feasibility/Safety and Validation of the Alfred Step Test Exercise Protocol (A-STEP) Developed for Adults With Cystic Fibrosis:
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 25, 2016 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Alfred
Collaborators
Monash University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Exercise testing has become clinically important in the management and ongoing evaluation of patients with Cystic Fibrosis (CF) with higher rates of exercise tolerance and participation previously linked to lower mortality risk (1). Lower exercise capacity generally correlates with more severe lung disease (2,3) and landmark studies suggest that low exercise capacity as measured by peak oxygen capacity (VO2peak) and rate of decline in lung function (FEV1) are strong predictors of mortality (1,4). However not all studies have found pulmonary function tests (PFTs) to be reliable predictors of maximal exercise capacity (5), especially in relatively well preserved lung function (6,7). The wide distribution in physical capacity between fit individuals and end stage disease adds to complexity of assessment. Independent factors of age, genetics, habitual exercise, nutritional status and musculoskeletal conditions are all known to influence physical capacity in patients with CF (8,9). Maximal exercise testing places additional stress on cardiovascular, respiratory and peripheral systems providing more information around multiple influences on disease progression including degree of limitation in these major systems (10,11) and is useful for assessment of exercise desaturation, more common (but not always present) in advanced lung disease (5,12). With prediction of exercise performance and functional capacity from PFTs unreliable and the understanding that health status correlates better with exercise tolerance there has been an increase in maximal exercise testing for patient management (13). Many international centers now regard exercise testing as highly important with many assessing maximal exercise capacity annually to monitor disease progression, identify physical status and drive changes in medical, physiotherapy or nutritional management (14,15). The main vision is to develop a standardized incremental step test protocol suitable for adults with Cystic Fibrosis (CF), all ages, levels of fitness and disease state that is in line with current exercise testing recommendations (15). To develop a more useful field test to assess exercise tolerance and a more "user friendly" test than the currently available laboratory exercise test to allow for early detection of decline in physical function in the day-to-day clinical setting. To date no studies have been published in adults with CF where an incremental exercise step test has been investigated to assess exercise tolerance or determine maximum oxygen uptake (VO2max).
Detailed Description
Many international centers now regard exercise testing as highly important with many measuring maximal exercise capacity annually to monitor disease progression, identify physical status and to drive changes in medical, physiotherapy or nutritional management (14,15). Cardiopulmonary Exercise Testing (CPET): The current best practice for assessing VO2max in adults with CF is a CPET using the Godfrey Protocol, a progressive and incremental maximal test performed on a cycle ergometer (13,14,15). Exercise testing should aim to achieve a maximal response within a time frame of 8-12 min and incremental protocols with stage duration of 1 minute are considered more efficient in eliciting the desired response within this time frame (14). During CPET, VO2max is determined while breath-by-breath gas analysis allows for a comprehensive assessment of exercise ventilation and circulation. This information can identify reasons for low exercise capacity and whether exercise limitation is due to deconditioning, or primarily within the respiratory, cardiovascular or peripheral systems. CPET is performed using a specialist ergometer, and requires specialist clinical expertise, monitoring and reporting equipment for interpretation of the test. The cost, space and expertise to carry out CPET in CF units around the world may limit its use for the regular assessment of exercise capacity in adults with CF (16). Field Tests: Field tests generally cannot determine absolute maximal exercise capacity, but do provide valuable information about the patient's functional abilities and limitations and compared to laboratory tests are inexpensive and easy to administer. Field tests that use a single step for assessment of exercise tolerance in patients with chronic lung disease include: 3-Minute Step Test (3MST): The 3MST is a feasible and acceptable measure of sub-maximal exercise performance in children and adults and a useful tool in the assessment of oxygen desaturation (17,18). The test is short in duration, simple to carry out, and has low cost and minimal space and equipment requirements however the sub-maximal nature and ceiling effect of the 3MST limits its usefulness clinically across the age spectrum (18,19). The Chester Step Test (CST): The CST is a 10-minute sub-maximal standardized multistage test and like the 3MST has minimal space and equipment requirements. The CST was originally designed for workplace screening and is now widely used for exercise prescription in the UK cardiac population (20). In healthy individuals one study reported a ceiling effect and a positive relationship between predicted VO2max using the CST and measured VO2max (21) however a subsequent study questioned this prediction validity (22). The CST has been found to be highly reproducible in patients with chronic obstructive lung disease (COPD) and reliable in patients with Bronchiectasis, but too challenging for both groups (23,24). The Modified Incremental Step Test (MIST): The MIST was designed to be more suitable for COPD patients and modeled from the CST(25). A reduction in work rate was not found to result in a difference in cardiopulmonary stress and exertion effort at peak exercise but did result in a higher exercise tolerance in patients with COPD. The MIST is reliable and better tolerated than the CST in patients with Bronchiectasis (23,24). The CST and CF: One study (published in abstract form) has shown the CST to be a useful field test when compared to the 3MST and 6MWT for those with mild to moderate CF. The authors commented this was likely due to the progressive nature being more representative of adult physical activity (26). The main vision is to develop a standardized incremental step test protocol suitable for adults with Cystic Fibrosis (CF), all ages, levels of fitness and disease state that is in line with current exercise testing recommendations (15). The test should be a more useful than the already available field tests and more "user friendly" test than the currently available laboratory exercise test to assess exercise tolerance and allow for early detection of decline in physical function in the day-to-day clinical setting. To date no studies have been published in adults with CF where an incremental exercise step test has been investigated to assess exercise tolerance or determine VO2max. To design a standardized externally paced incremental step test that is portable, easy to administer, simple to perform, time, cost and space efficient (A-STEP). Study A: To assess feasibility and reliability of the A-STEP to objectively assess exercise tolerance. To determine if the A-STEP is a more useful tool than the 3-Minute Step Test. Study B: To develop an alternative tool to determine maximum oxygen uptake (VO2max) to the "gold standard" CPET that is feasible across the whole spectrum of lung disease. To determine if the A-STEPmax is a valid tool when compared to the VO2max achieved from a CPET performed on a cycle ergometer using the Godfrey Protocol. The principle investigator hypothesizes that the A-STEP will be a feasible tool to assess exercise capacity; and the A-STEP max will be a valid tool for the assessment of VO2max across the age range and disease spectrum in adults with CF.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Fibrosis, Lung Diseases, Respiratory Diseases, Genetic Diseases, Pancreatic Diseases
Keywords
Exercise Testing, Maximal Exercise Testing, Maximal Exercise Capacity, Peak Exercise Capacity, Adults, Step Tests

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A-STEP
Arm Type
Experimental
Arm Description
Study A) A-STEP Study Development of new exercise test protocol and Observational Feasibility/Safety Study (no comparator).
Arm Title
A-STEP (New Protocol)
Arm Type
Experimental
Arm Description
Study B) A-STEPmax Study Validity Study (random allocation of test order).
Arm Title
CPET cycle ergometer (Gold Standard)
Arm Type
Active Comparator
Arm Description
Study B) A-STEPmax Study Validity Study (random allocation of test order).
Intervention Type
Other
Intervention Name(s)
A-STEP
Other Intervention Name(s)
Alfred Step Test Exercise Protocol (A-STEP)
Intervention Description
Study A) Study A) Development of new exercise test protocol and Observational Feasibility/Safety Study (no comparator). Feasibility/safety of a newly designed, incremental, maximal, standardised step test in adults with Cystic Fibrosis.
Intervention Type
Other
Intervention Name(s)
A-STEP (New Protocol)
Other Intervention Name(s)
Alfred Step Test Exercise Protocol
Intervention Description
Study B) Validation Study (random allocation of test order). Validity of an incremental, maximal, standardised incremental step test with breath-by-breath gas analysis using portable metabolic measurement equipment against CPET.
Intervention Type
Other
Intervention Name(s)
Comparator: CPET cycle ergometer (Gold Standard)
Other Intervention Name(s)
Cardiopulmonary Exercise Test Protocol
Intervention Description
Study B) Validation study (random allocation of test order) "Gold standard" CPET. An incremental, maximal standardised cycle ergometer exercise test (performed as per published protocol) using portable metabolic measurement equipment.
Primary Outcome Measure Information:
Title
Study B) Maximum oxygen uptake (VO2max)
Description
The highest oxygen uptake achieved during the exercise test taken from inspired gas in a given period of time. Body weight is used to calculate this from oxygen consumption during the test. VO2peak may be used as a surrogate if VO2max is not achieved. Criteria for reaching maximum effort is not included in this document.
Time Frame
Measured during the incremental test for a maximum of 15 minutes.
Title
Study A) Oxygen Saturation
Description
Standard objective outcome measures of field exercise testing. Measured via pulse oximetry.
Time Frame
Measured for 3 min prior to exercise (recorded at baseline sitting and standing), monitored during the test (recorded at minute intervals) and for at least 2 min of recovery up to a maximum of 10 minutes.
Title
Study A) Heart Rate
Description
Standard objective outcome measures of field exercise testing. Measured via pulse oximetry.
Time Frame
Measures for 3 min prior to exercise (recorded at baseline sitting and standing), monitored during the test (recorded at minute intervals) and for at least 2 min of recovery up to a maximum of 10 minutes.
Secondary Outcome Measure Information:
Title
Study B) Carbon Dioxide Production
Description
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis with portable metabolic measurement equipment.
Time Frame
Measured during the test incremental tests for a maximum 15 minutes and 5 mins of recovery.
Title
Study B) Respiratory Exchange Ratio
Description
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis. The ratio of carbon dioxide production to oxygen consumption.
Time Frame
Measured during the test incremental tests for a maximum 15 minutes and 5 mins of recovery.
Title
Study B) Minute Ventilation
Description
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis. The product of tidal volume and respiratory rate.
Time Frame
Measured during the test incremental tests for a maximum 15 minutes and 5 mins of recovery.
Title
Study B) Oxygen Pulse
Description
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis. Calculated by dividing the oxygen consumption by heart rate.
Time Frame
Measured during the test incremental tests for a maximum 15 minutes and 5 mins of recovery.
Title
Study B) Tidal Volume
Description
Standard secondary outcome measure of maximal exercise testing using breath- by-breath gas analysis. The volume of each breath taken.
Time Frame
Measured during the test incremental tests for a maximum 15 minutes and 5 mins of recovery.
Title
Study B) Oxygen Saturation
Description
Standard objective outcome measures of exercise testing. Measured via pulse oximetry.
Time Frame
easures are taken at baseline (post 5 mins), monitored during the test (recorded at minute intervals) and for min 5 mins of recovery
Title
Study B) Heart rate
Description
Standard objective outcome measures of exercise testing. Measured via pulse oximetry.
Time Frame
easures are taken at baseline (post 5 mins), monitored during the test (recorded at minute intervals) and for min 5 mins of recovery
Title
Study B) Measures from Electrocardiogram
Description
Used to monitor the patient's cardiac rhythm (CPET only)
Time Frame
easures are taken at baseline (post 5 mins), monitored during the test (recorded at minute intervals) and for min 5 mins of recovery
Title
Study A & B) Breathlessness and Leg Fatigue
Description
Standard subjective outcome measures of exercise testing. Modified Borg 0-10.
Time Frame
Measures are taken at baseline (post 5 mins), monitored during the test (recorded at minute intervals) and for min 5 mins of recovery
Title
Study A & B) Blood pressure
Description
Standard outcome measure of exercise testing.
Time Frame
Measures are takenpre/post A-STEP, pre/every 2 mins during/post CPET
Title
Study A & B) Duration of test; Highest level (mins and sec)/stage achieved; Reason for test termination.
Description
Parameters of exercise test.
Time Frame
Measured during or on completion of the test. Maximum 15 minutes.
Other Pre-specified Outcome Measures:
Title
Study A & B) Gender; Age, Height, BMI, fitness level
Description
Demographic baseline descriptive measures.
Time Frame
Recorded on the day of testing maximum 10 mins.
Title
Study A & B) Spirometry (Pulmonary Function Tests)
Description
Baseline Pulmonary Function Test measures.
Time Frame
Recorded on the day of testing prior to testing, maximum 10 minutes Study B. Most recent PFTs if day of testing lung function is not available study A.
Title
Study A & B) Alfred Wellness Score for CF (AweScore CF)
Description
Alfred specific clinical tools: quality of life measure.
Time Frame
Recorded on the day of testing prior to testing, maximum 2 minutes.
Title
Study A) Musculoskeletal Assessment Tool-Quick Screen
Description
Alfred specific clinical tool: to screen for musculoskeletal issues.
Time Frame
Recorded on the day of testing, maximum 20 minutes.
Title
Study A & B) Medical history.
Description
Baseline descriptive measures of health status.
Time Frame
Recorded on the day of testing, maximum 10 minutes.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION Confirmed Diagnosis of CF (by genotype or positive sweat test) Aged 18yrs and older FEV1 ≥20% (Forced expiration in 1 sec) Stable baseline state. (Stable baseline state is defined as: clinically stable respiratory status, for at least 30 days, characterized by the absence of hospitalization and no changes in maintenance therapy during this period (Yankaskas et al 2004)). EXCLUSION Febrile Haemoptysis Uncontrolled asthma Pneumothorax Cardiac issues Unreliable readings on pulse oximetry Pulmonary hypertension Unstable CF related diabetes (CFRD) Vascular issues Renal disease Pregnancy Body mass index (BMI) <18.0 Significant musculoskeletal issues Unable to safely follow instructions (ATS/ACCP 2003; Hebestreit 2015)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lisa M Wilson, BHS(Physio)
Phone
0390763450
Ext
5650
Email
l.wilson@alfred.org.au
First Name & Middle Initial & Last Name or Official Title & Degree
Dr Brenda M Button, PhD
Phone
0390763450
Ext
4601
Email
b.button@alfred.org.au
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lisa M Wilson, BHS(Physio)
Organizational Affiliation
Alfred Hospital; Monash University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Alfred Hospital
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3004
Country
Australia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lisa M Wilson, BHS(Physio)
Phone
0390763450
Ext
5650
Email
l.wilson@alfred.org.au
First Name & Middle Initial & Last Name & Degree
Dr Brenda M Button
Phone
0390763450
Ext
4601
Email
b.button@alfred.org.au
First Name & Middle Initial & Last Name & Degree
Lisa M Wilson, BHS(Physio)
First Name & Middle Initial & Last Name & Degree
Dr Brenda M Button, PhD
First Name & Middle Initial & Last Name & Degree
Professor John W Wilson, MBBS, PhD
First Name & Middle Initial & Last Name & Degree
Dr Rebecca Lane, PhD, BPhysio
First Name & Middle Initial & Last Name & Degree
A/Prof Shapour Jaberzadeh, PhD, M.AppSc

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No plan to share individual patient data.
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The Alfred Step Test Exercise Protocol (A-STEP), for Adults With Cystic Fibrosis.

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