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This is a study to evaluate whether exercise training and education program have beneficial effects upon the quality of life and exercise capacity in patients with chronic obstructive lung disease

â??â??Comprehensive Assessment of Clinical Outcomes Following Hospital Based Structured Pulmonary Rehabilitation Program in Patients with Moderately Severe Chronic Obstructive Pulmonary Disease and Strategies for Field-level Implementationâ??â??

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/08/020755
Enrollment
78
Registered
2019-08-19
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: O- Medical and Surgical Health Condition 2: null- Patients with moderately severe chronic obstructive pulmonary disease

Interventions

Intervention1: Rehabilitation intervention: Patients with moderately severe chronic obstructive pulmonary disease who will be provided offered rehabilitation on top of usual standard of care from the

Sponsors

Dept of Pulmonary Medicine and Sleep Disorders All India Institute of Medical Sciences New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i. Moderately severe COPD in stable state or following recovery from acute episode ii. No evidence of recent respiratory tract infection (within the last 6 weeks) iii. Subjects possessing cognitive ability to comprehend and follow advice iv. They should have the motivation and willingness to participate in the study v. Patients living in Delhi / NCR area, preferably for ease of follow-up

Exclusion criteria

Exclusion criteria: i.Subjects with co morbid conditions â?? uncontrolled hypertension, diabetes, ischemic cardiac disease, acute cor-pulmonale, severe pulmonary hypertension, significant hepatic dysfunction, metastatic cancer, renal failure, severe anemia, severe cognitive deficit, and psychiatric disease that interferes with memory and compliance. ii.Subjects with significant neuromuscular and skeletal problems who are unable to perform the exercises. iii.Not willing to give written informed consent.

Design outcomes

Primary

MeasureTime frame
i.Exercise Capacity, measured by a.Maximum oxygen uptake during CPET (VO2max) b.Six minute walk distance (6MWD) ii.Quality of Life, measured by a.SGRQ score Timepoint: Outcome parameters will be measured at two time points: Firstly at baseline and then after completion of two months of the proposed intervention.—

Secondary

MeasureTime frame
a. BMI b. Anthropometry c. Mid arm circumference d. Skin fold thickness a. mMRC grade b. Spirometry c. 6 minute walk distanceTimepoint: Outcome parameters will be assessed at two time points: firstly, at the baseline, and then after completion of two months of the proposed intervention.—

Countries

India

Contacts

Public ContactDr Anant Mohan

All India Institute of Medical Sciences

anantmohan@yahoo.com1126593006

Outcome results

None listed

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