Comparison Of Coughing and Active Cycle of Breathing Technique to Improve Pulmonary Functions in Post-Surgical Patients

• Sponsor: Superior University (Other)
• Overall Status: Recruiting
• CT.gov ID: NCT05875831
• Collaborator: (none)
• Enrollment: 58
• Location: 1
• Arms: 2
• Anticipated Duration (Months): 5
• Patients Per Site Per Month: 11.6

Study Details

Study Description

Brief Summary

To find out the Comparison Of Coughing and Active Cycle of Breathing Technique to Improve Pulmonary Functions in Post-Surgical Patients

Condition or Disease	Intervention/Treatment	Phase
Post Surgical	Behavioral: Active Cycle of Breathing; Diagnostic Test: Coughing	N/A

Study Design

• Study Type: Interventional
• Anticipated Enrollment: 58 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: None (Open Label)
• Primary Purpose: Health Services Research
• Official Title: Comparison Of Coughing and Active Cycle of Breathing Technique to Improve Pulmonary Functions in Post-Surgical Patients
• Actual Study Start Date: Apr 1, 2023
• Anticipated Primary Completion Date: Jun 1, 2023
• Anticipated Study Completion Date: Aug 31, 2023

Arms and Interventions

Arm	Intervention/Treatment
Other: Coughing	Diagnostic Test: Coughing; Coughing to Improve Pulmonary Functions in Post-Surgical Patients
Experimental: Active Cycle of Breathing	Behavioral: Active Cycle of Breathing; Active Cycle of Breathing Technique to Improve Pulmonary Functions in Post-Surgical Patients

Outcome Measures

Primary Outcome Measures

1. Spirometry-related questions [6 Months]

2. surgical Related Questioner [6 Months]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 50 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Both male and female between the age of 18-50 years who reported post-surgical complications related to pulmonary will be selected in this study

Exclusion Criteria:

• If patient is unresponsive, psychologically disturbed and does not want to participate, teenagers will be excluded from this study

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Chaudary Muhammad Akram Teaching Hospital	Lahore	Punjab	Pakistan

Sponsors and Collaborators

• Superior University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Muhammad Naveed Babur, Principal Investigator, Superior University
• ClinicalTrials.gov Identifier: NCT05875831
• Other Study ID Numbers: DPT/Batch-Fall18/543
• First Posted: May 25, 2023
• Last Update Posted: May 25, 2023
• Last Verified: May 1, 2023

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: No
• Studies a U.S. FDA-regulated Device Product: No
• Additional relevant MeSH terms: Cough

Study Results

No Results Posted as of May 25, 2023