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Respiratory Muscle Training and Walking Exercise in Women Recovering From COVID-19 Pneumonia
Respiratory Muscle Training and Walking Exercise in Women Recovering From COVID-19 Pneumonia

NCT07656610

CompletedNA

Sponsor: Hitit University

Conditions: COVID-19 Pneumonia, Respiratory Symptoms

Interventions: Respiratory Muscle Training, Walking Exercise

Countries: Turkey (Türkiye)

This experimental study was designed to investigate the effects of respiratory muscle training and walking exercise on selected blood, respiratory, functional, dyspnea, sleep quality, and quality-of-life outcomes in women who had recovered from COVID-19-related lung inflammation/pneumonia. The study included women aged 20 to 45 years who had experienced COVID-19 with pneumonia, reported dyspnea, and had reduced quality of life. A total of 80 female participants were divided into four groups: respiratory muscle training plus walking exercise, respiratory muscle training alone, walking exercise alone, and a control group, with 20 participants in each group. Measurements were performed before and after the intervention period. The assessments included pulmonary function testing, maximal inspiratory pressure, the 6-minute walk test, the modified Borg scale for dyspnea, the Nottingham Health Profile, the Pittsburgh Sleep Quality Index, and selected blood parameters. The study aimed to determine whether respiratory muscle training, walking exercise, or their combination could improve respiratory function, inspiratory muscle strength, functional capacity, dyspnea, sleep quality, quality of life, and blood-related parameters in this population.

Eligibility overview

Sex: FEMALE

Age: 20 Years to 45 Years

Healthy volunteers: No

Study type: INTERVENTIONAL

Eligibility criteria
Inclusion Criteria:

* Female participants aged 20 to 45 years
* History of COVID-19-related pneumonia
* Presence of dyspnea after COVID-19
* Modified Borg dyspnea score between 1 and 7 after the 6-minute walk test
* Resting oxygen saturation between 90% and 95%
* Incomplete resolution of COVID-19-related lesions on chest radiography
* Voluntary agreement to participate in the study
* Signed written informed consent form

Exclusion Criteria:

* Modified Borg dyspnea score between 0 and 1
* Modified Borg dyspnea score greater than 7
* History of chronic obstructive pulmonary disease, heart failure, or pulmonary fibrosis causing dyspnea before COVID-19 pneumonia
* Upper abdominal or thoracic surgery within the previous 3 months
* Cancer
* Pregnancy
* Presence of another disease contributing to dyspnea in addition to COVID-19-related dyspnea
* Cardiovascular, musculoskeletal, or nervous system involvement related to COVID-19
* Mental disorder or mental instability
* Language barrier preventing understanding of Turkish
* Refusal to participate or withdrawal from the study at any stage
* History of being a competitive athlete
* Lack of voluntary participation or refusal to sign the written informed consent form
Locations (1)
  • Çorum, Çorum, Turkey (Türkiye)