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Effectiveness of short duration of pulmonary rehabilitation in chronic lung disease patients - A 1 year study

Not Applicable
Suspended
Conditions
Health Condition 1: J479- Bronchiectasis, uncomplicatedHealth Condition 2: J432- Centrilobular emphysemaHealth Condition 3: J449- Chronic obstructive pulmonary disease, unspecifiedHealth Condition 4: J841- Other interstitial pulmonary diseases with fibrosisHealth Condition 5: J455- Severe persistent asthma
Registration Number
CTRI/2020/03/023706
Lead Sponsor
Dr Nagesh Dhadge
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Suspended
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patients between the age groupof 40-80 years fromboth gender

Physician diagnosed chronic respiratory conditions from the above list

mMRC(modified Medical Research Council ) dyspnea scale of 1 and more

Subjects willing to participate in once a week supervised pulmonary rehabilitation program

Exclusion Criteria

Inability to provide consent for the PR program

Recent acute myocardial infarction or cardiac intervention within four weeks

Any major surgery within last four weeks

Presence of severe arthritis or severe peripheral vascular disease

Severe psychiatric or cognitive affection or inability to follow instructions in PR

Any other clinical observation in the opinion of treating physician precluding safe PR

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.Determine outcomes in Saint George Respiratory Questionnaire (SGRQ) in once-a-week supervised outpatient pulmonary rehabilitation in chronic respiratory diseases in resource constraint primary care settings over a period of one year. <br/ ><br>2.Determine change in 6 minute walk distance after one year of PR <br/ ><br>Timepoint: Baseline, 6 months, 1 year
Secondary Outcome Measures
NameTimeMethod
1.To study change in mMRC dyspnea scale after PR in CRD <br/ ><br>2.To compare the change in fatigue score ( FACITver 4 )after PR <br/ ><br>3.To compare healthcare utilisation one year before and after completing PR in patients with CRD in terms of <br/ ><br>4.To study compliance of short duration supervised once a week outpatient PR. <br/ ><br>5.To study feedback of patients on PR in primary care setting. <br/ ><br>Timepoint: Baseline, 6 months, 1 year
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