NCT05875831

Brief Summary

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

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Apr 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 18, 2023

Completed
14 days until next milestone

Study Start

First participant enrolled

April 1, 2023

Completed
2 months until next milestone

First Posted

Study publicly available on registry

May 25, 2023

Completed
7 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2023

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 31, 2023

Completed
Last Updated

May 25, 2023

Status Verified

May 1, 2023

Enrollment Period

2 months

First QC Date

March 18, 2023

Last Update Submit

May 16, 2023

Conditions

Post Surgical

Outcome Measures

Primary Outcomes (2)

  • Spirometry-related questions

    6 Months

  • surgical Related Questioner

    6 Months

Study Arms (2)

Coughing

OTHER
Diagnostic Test: Coughing

Active Cycle of Breathing

EXPERIMENTAL
Behavioral: Active Cycle of Breathing

Interventions

Active Cycle of BreathingBEHAVIORAL

Active Cycle of Breathing Technique to Improve Pulmonary Functions in Post-Surgical Patients

Active Cycle of Breathing
CoughingDIAGNOSTIC_TEST

Coughing to Improve Pulmonary Functions in Post-Surgical Patients

Coughing

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Chaudary Muhammad Akram Teaching Hospital

Lahore, Punjab Province, Pakistan

RECRUITING

Central Study Contacts

Muzammil Arshad, DPT

CONTACT

+923144248803muzammilarshadvirk055@gmail.com

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

March 18, 2023

First Posted

May 25, 2023

Study Start

April 1, 2023

Primary Completion

June 1, 2023

Study Completion

August 31, 2023

Last Updated

May 25, 2023

Record last verified: 2023-05

Data Sharing

IPD Sharing
Will not share

Locations

PA(1)