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Effect of rehabilitation with and without Non Invasive Ventilation among COPD subjects

Effect of rehabilitation with and without Non Invasive Ventilation on change in pulmonary function and CAT scores of COPD patients at Masih Daneshvari Hospital

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016102927929N3
Enrollment
50
Registered
2017-02-14
Start date
2016-09-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Chronic obstructive pulmonary disease. Chronic obstructive pulmonary disease, unspecified

Interventions

Intervention 1: Control group: 3 session/week for 3 weeks of rehabilitation including respiratory exercise and exercise therapy and Non invasive ventilation mask while the device is off. Intervention
Treatment - Devices
Control group: 3 session/week for 3 weeks of rehabilitation including respiratory exercise and exercise therapy and Non invasive ventilation mask while the device is off.
Intervention group: 3 sessions/ week for 3 weeks of rehabilitation including respiratory exercise and exercise therapy and Non Invasive Ventilation while the device is on.

Sponsors

Vice Chancellor for research ofShahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: identifying chronic obstructive pulmonary disease; the satisfaction of participating in the study; The Consciousness of subjects Exclusion criteria: inability to carry out rehabilitation; the occurrence of exacerbation or disease attack

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Distance covered during 6 minutes. Timepoint: Before and immediately after intervention. Method of measurement: six minute walk test.;COPD assessment test score. Timepoint: Before and immediately after intervention. Method of measurement: COPD assessment test questionnaire.

Secondary

MeasureTime frame
Forced expiatory volume in 1st second. Timepoint: Before and immediately after intervention. Method of measurement: spirometry.;Pressure of CO2. Timepoint: Before and immediately after intervention. Method of measurement: Venus blood gas.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Atefeh Fakharian

Shahid Beheshti University of Medical Sciences

fakharian_2005@yahoo.com+98 21 2610 5050

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 27, 2026