ULTH
Lahore, Punjab Province, Pakistan
NCT Number: NCT07716696
Pericarditis is associated with symptoms such as chest pain, dyspnea, fatigue, cough, and anxiety, which can significantly impair functional capacity and quality of life. Pulmonary rehabilitation is a structured intervention designed to improve respiratory function and overall physical performance. This study aims to compare the effectiveness of pulmonary rehabilitation versus standard care in improving clinical symptoms and functional outcomes in patients with pericarditis.
This study is active but is not currently recruiting participants.
18 year–65 year
All sexes
Interventional
Not applicable
Lahore, Punjab Province, Pakistan
This randomized controlled trial evaluates the comparative effectiveness of pulmonary rehabilitation and standard care in patients diagnosed with pericarditis. Participants are allocated into two groups: an intervention group receiving pulmonary rehabilitation and a control group receiving standard medical care.
Pulmonary rehabilitation includes breathing exercises, aerobic training, and patient education aimed at improving respiratory efficiency and reducing symptom burden. Such programs are widely used to improve functional capacity and quality of life in clinical populations [1].
Outcome measures include pain intensity, dyspnea, cough severity, fatigue, and anxiety, assessed using validated tools such as the Visual Analog Scale (VAS) and McMaster Cough Severity Questionnaire.
Assessments will be conducted at baseline and after completion of the intervention period.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Diagnosed with pericarditis Age between 18-65 years Both male and female participants Medically stable Able to participate in rehabilitation Willing to provide informed consent
Exclusion criteria
Severe cardiovascular or respiratory instability Other major pulmonary diseases Recent surgery or trauma Neurological disorders affecting participation Unwillingness to participate
A structured program including breathing exercises, aerobic conditioning, and patient education administered over multiple weeks.
Routine clinical management as prescribed by the treating physician without additional rehabilitation protocol.
Time frame: Baseline and 8 weeks
Measured using Visual Analog Scale (VAS)
Time frame: Baseline and 8 weeks
Measured using VAS
Time frame: Baseline and 8 weeks
Measured using McMaster Cough Severity Questionnaire
Time frame: Time Frame: Baseline and 8 weeks
Measured using VAS or standardized fatigue scale
Time frame: Time Frame: Baseline and 8 weeks
Measured using a validated anxiety scale
University of Lahore
Other
Comparative Effects of Pulmonary Rehabilitation Versus Standard Care on Pain, Dyspnea, Cough Severity, Fatigue, and Anxiety in Patients With Pericarditis: A Randomized Controlled Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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