The effect of respiratory exercises on quality of life in in covid-19 patients

The effect of respiratory exercises on quality of life in covid-19 patients

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20211201053238N1

Enrollment

Registered

2022-01-10

Start date

2021-12-11

Completion date

Unknown

Last updated

2022-02-07

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

Conditions

Covid-19. COVID-19, virus identified: COVID-19 has been confirmed by laboratory testing irrespective of severity of clinical signs or symptoms. Use additional code, if desired, to identify pneumonia or other manifestations. Coronavirus disease (COVID-19) is an inf

Interventions

In this semi-experimental clinical trial, intervention will be performed in the first week (2 days a week, Sundays and Tuesdays) and each session for 45-60 minutes in clinic by the researcher with the

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Patients must be referred to the department of physical medicine and rehabilitation in Shohade Tajtish Hospital Patients must be recovered from corona (after 3 weeks and under 18 weeks) and after hospitalization Patients must be between the ages of 18 and 75 Patient satisfaction must be obtained to participate in the research None of the patients should have been treated for pulmonary rehabilitation

Exclusion criteria

Exclusion criteria: None of the patients have problems against pulmonary massage, including; active wounds, fractures and skin disorders in the chest area Patients do not have a history of uncontrolled cardiovascular problems, chronic pulmonary, renal, neurological, hypertension, acute rheumatological, psychological phases leading to not doing exercise

Design outcomes

Primary

Measure	Time frame
Quality of life. Timepoint: Before and 2 weeks after intervention. Method of measurement: The RAND 36-item health survey (SF-36 health survey).	—

Secondary

Measure	Time frame
Level of Blood Oxygen. Timepoint: Before and 2 weeks after intervention. Method of measurement: Pulse Oximeter instrument.;Heart Rate. Timepoint: Before and 2 weeks after intervention. Method of measurement: Pulse Oximeter instrument.;Level of Dyspnea. Timepoint: Before and 2 weeks after intervention. Method of measurement: Borg Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactLeila Angooti Oshnari

Shahid Beheshti University of Medical Sciences

leylaa1768@yahoo.com+98 21 2272 4208

Outcome results

None listed

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