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A clinical trial to identify factors affecting quality of life in COPD.

COPD:Effect of circuit training on various identified factors and quality of life. - CT-PR-COPD

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/09/015707
Enrollment
52
Registered
2018-09-13
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: J40-J47- Chronic lower respiratory diseases

Interventions

Intervention1: Conventional Physiotherapy with Circuit training: Conventional Pulmonary rehabilitation including patient education, breathing retraining, endurance training in form of circuit (structu

Sponsors

Dept of Physiotherapy DYPatil University
Lead Sponsor
Prof Head Dept of Respiratory Medicine
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Patients with spirometry confirmed COPD GOLD catgory 1,2,3,4. smokers and ex-smokers with smoking history of more than 10 pack years. Duration/onset of symptoms more than 5 years.

Exclusion criteria

Exclusion criteria: Individuals with acute or recent history of acute exacerbations. patients with co-existence of other chronic respiratory diseases(Asthma, TB) with impaired pulmonary function. individual with diagnosed cancer, uncontrolled hypertension, diabetes mellites, cardio-vascular, neurological and/or osteoarticular diseases with functional limitations precluding safe testing.individuals receiving home oxygen therapy.known psychiatric illness, cognitive limitations and lack of motivation.individials not willing to participate.

Design outcomes

Primary

MeasureTime frame
Functional capacity as measured by Six minute walked distance(6MWD)and Quality of life as measured by St. Georges Respiratory QuestionnaireTimepoint: Before starting the intervention and after eight weeks of intervention.

Secondary

MeasureTime frame
Sleep quality as measured by Pittsburg sleep quality indexTimepoint: Before starting the intervention and after eight weeks of intervention.

Countries

India

Contacts

Public ContactPooja Akhtar

N.K.P.Salve Institute of Medical sciences and Lata Mangeshkar Hospital, Digdoh Hills, Hingna, Nagpur

poojaakhtarvspm@gmail.com91-9665038090

Outcome results

None listed

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