The primary aim of this pilot randomized controlled trial is to determine feasibility of the proposed pulmonary rehabilitation intervention.
In this pilot randomized controlled trial, our primary aim is to determine feasibility of the proposed intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
56
Use of HFO
Room air or normal flow oxygen
Changi General Hospital
Singapore, Singapore
RECRUITINGChanges in 1-minute sit to stand test
maximum number of sit to stand cycles in 1 minute
Time frame: 1 month
Changes in 30-second sit to stand test
maximum number of sit to stand cycles in 30 seconds
Time frame: 1 month, 3 month
Changes in respiratory symptoms
Modified Medical Research Council Dyspnea Scale. The scale ranges from 0 to 4 with a higher score indicating increasing breathlessness
Time frame: 1 month, 3 months
Changes in mood
Hospital Anxiety Depression Scale. The scale ranges from 0 to 21, A total subscale score of \>8 points indicates considerable symptoms of anxiety or depression.
Time frame: 1 month, 3 month
changes in quality of life
EQ-5D-5L
Time frame: 1 month, 3 month
Changes in lung function
Forced expiratory volume in 1 sec
Time frame: 1 month, 3 month
Changes in lung function
forced vital capacity
Time frame: 1 month, 3 month
Proportion of patients who still have exertional hypoxemia
Comparing the proportion of patients who still have exertional hypoxemia
Time frame: 1 month, 3 month
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Adherence rates
Comparing the adherence rates between the 2 study arms
Time frame: 3 week
Changes in 1-minute sit to stand test
maximum number of sit to stand cycles in 1 minute
Time frame: 3 month