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Pulmonary rehabilitation in low resource settings for people with breathlessness due to lung conditions

Pulmonary rehabilitation delivered in low resource settings for people with chronic respiratory disease: a 3-arm assessor-blind randomised implementation trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075277
Enrollment
117
Registered
2024-10-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J449- Chronic obstructive pulmonary disease, unspecified

Interventions

Intervention1: Center based pulmonary rehabilitation.: Intervention delivered at study centre. Twice a week for total 8 weeks. It is comprehensive, multidisciplinary, individually-tailored interventio

Sponsors

Medical Research Council
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Adults 18years old (the age of majority in all the countries). No upper age limit. • Assessed by referring physician as having persistent and functionally limiting respiratory symptoms (mMRC more than 2) after optimisation of pharmacological therapy. • Resident locally and willing to engage with either Centre-PR and Home-PR schedules if randomised to either of these groups. • Willing and able to provide written informed consent.

Exclusion criteria

Exclusion criteria: • People with non-respiratory causes for the symptoms (stable co-morbidity may be included if clinically appropriate). • Active TB infection. • Any condition that would increase risk (e.g. uncontrolled cardiac disease) interfere with PR (e.g. neurological disorders, severe arthritis, dementia).[44] or be inappropriate (very severe frailty, end-of-life) • On-going, or completed PR (including other exercise programme) within previous 18 months. • Living in the same house as another participant • Unwilling or unable to provide informed consent.

Design outcomes

Primary

MeasureTime frame
Endurance Shuttle Walking Test (ESWT)Timepoint: 8 weeks post intervention and 6 months post intervention

Secondary

MeasureTime frame
Health related quality of life (HRQoL);anxiety/depression level, breathlessness level, physical activity levelTimepoint: 8 weeks post intervention and 6 months post intervention

Countries

India

Contacts

Public ContactParag Gajanan Khatavkar

KEM Hospital Research Centre

p.khatavkar@kemhrcpune.org9890141514

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026