Description Module

Description Module

The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.

Description Module path is as follows:

Study -> Protocol Section -> Description Module

Description Module


Ignite Creation Date: 2025-12-25 @ 12:45 AM
Ignite Modification Date: 2025-12-25 @ 12:45 AM
NCT ID: NCT06191367
Brief Summary: 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.
Detailed 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.
Study: NCT06191367
Study Brief:
Protocol Section: NCT06191367