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To study the effectiveness of pulmonary rehabilitation program in people who have recovered from covid 19 pneumonia and Acute Respiratory Distress

Not Applicable
Conditions
Health Condition 1: F- Physical Rehabilitation and Diagnostic Audiology
Registration Number
CTRI/2020/12/029957
Lead Sponsor
Department of PMR
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

With definitive radio logical evidence of covid pneumonia

with proved covid 19 positive swab,completed 10 days of admission in isolation ward

Willing to participate in rehabilitation

Hemodynamically stable

Mini-mental state examination (MMSE) score > 21

Age between 18 and 80 years

Exclusion Criteria

5)Resting Respiratory rate >30/min

4)SpO2 at rest in room air <85%

2)Fever, temperature >100â??F

6)Moderate or severe heart disease (Grade III or IV, NYHA)

1)Patients who are in acute respiratory distress phase/critical phase , requiring invasive or non invasive ventilation, in covid /suspect ICU/SARI ward

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Single breath count <br/ ><br>Breath holding Time, <br/ ><br>Respiratory rate , <br/ ><br>Modified Borg scale of dyspnoea at rest and after exertion, <br/ ><br> Dyspnoeic index <br/ ><br>Timepoint: baseline,1 week,2 weeks,3 weeks post rehabilitation
Secondary Outcome Measures
NameTimeMethod
AEROBIC ENDURANCE/SECONDARY PARAMETER <br/ ><br>6 minutes walk test / one minute walk test, <br/ ><br> FUNCTIONAL/SECONDARY OUTCOME MEASURES- <br/ ><br>sit to stand. <br/ ><br>Barthel Index <br/ ><br>Timepoint: pre and post rehabilitation
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