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Effect of Aerobic Exercises Versus Incentive Spirometer Device on Post-covid Pulmonary Fibrosis Patients

M

McCarious Nahad Aziz Abdelshaheed Stephens

Status

Active, not recruiting

Conditions

Post-COVID-19 Syndrome
Lung Fibrosis Interstitial

Treatments

Other: Traditional Chest Physiotherapy
Other: Aerobic Exercises
Device: Incentive Spirometer Device

Study type

Interventional

Funder types

Other

Identifiers

NCT06191367
CairoU post-covid PF Rehab

Details and patient eligibility

About

the aim of this study will be to investigate the effect of aerobic exercises vs incentive spirometer device on post-covid patients with residual lung diseases.

Full description

To our knowledge, there have been no enough studies that investigated the effect of aerobic exercise and incentive spirometer in pulmonary rehabilitation on post-covid syndrome patients.

Therefore, this study may open up ways to other researchers to investigate and build up on this effect if present and address such an important issue.

The finding of this proposed work may help patients with post-covid syndrome and complain of lung diseases by addressing their complains of symptoms like chest pain, dyspnea, and cough and provide a possible solution to enhance their quality of life and increase their participation in daily life activities.

Patients of post-covid syndrome with residual lung problems will be recruited after approval of ethical committee of the faculty of physical therapy, Cairo university. All participants will sign a written informed consent form.

The subjects will be randomly assigned into one of three groups:

  • Group I (experimental) will receive aerobic exercises program and traditional chest physiotherapy.
  • Group II (experimental) will receive incentive spirometer device treatment and traditional chest physiotherapy.
  • Group III (control) will receive traditional chest physiotherapy only. The measures will be taken before and after treatment program.

Enrollment

45 estimated patients

Sex

All

Ages

40 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hemodynamic stable (MAP not less than 60mmHg, systolic pressure >80mmHg and diastolic pressure not <60mmHg)
  • Age from 40 to 85 years.
  • Both sexes.
  • All patients were positive covid-19 infected patients and passed at least 4 weeks after confirmation.
  • All patients suffer from respiratory complications.
  • All patients included are actively breathing.
  • All patients included are fully aware and conscious.

Exclusion criteria

  • Hemodynamic Instability.
  • Severe Head Injury.
  • Increased intracranial pressure.
  • Anemic Hb<8.
  • Active Smoking.
  • Severe Bronchospasm.
  • Low BP (systole <80, diastole <60).
  • Subcutaneous Emphysema.
  • Rip Fractures.
  • Untreated Pneumothorax.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

45 participants in 3 patient groups

Group I (experimental) Aerobic Exercises and Traditional Chest Physiotherapy.
Experimental group
Description:
It was consisted of fifteen patients with positive covid-19 test from at least a month before trial. They received aerobic exercise techniques which consist of 3 levels of activity exercises and traditional program of chest physiotherapy. (Five times per week for two months).
Treatment:
Other: Traditional Chest Physiotherapy
Other: Aerobic Exercises
Group II (experimental)Incentive Spirometer Device and Traditional Chest Physiotherapy.
Experimental group
Description:
It was consisted of fifteen patients with positive covid-19 test from at least a month before trial. They received incentive spirometer training techniques and traditional program of chest physiotherapy. (Five times per week for two months).
Treatment:
Other: Traditional Chest Physiotherapy
Device: Incentive Spirometer Device
Group III (control) will receive Traditional Chest Physiotherapy only.
Active Comparator group
Description:
As a control group it was consisted of fifteen patients with positive covid-19 test from at least a month before trial. They received traditional program of chest physiotherapy only. (Five times per week for two months). for example: - Breathing Exercises. - Postural Drainage. - Percussion. - Coughing - Vibration.
Treatment:
Other: Traditional Chest Physiotherapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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