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Scapular Mobilization on Inspiratory Capacity of Post-CABG Patients

Primary Purpose

CABG

Status
Completed
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Conventional Treatment
Scapular Mobilization
Sponsored by
Riphah International University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for CABG

Eligibility Criteria

40 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • CAD patients undergone CABG surgery (Post-Op. Day#. 01).
  • Both genders (male and female).
  • Aged between 40 to 70 years .
  • Patient having oxygen saturation (SPO2) of more than or equal to 90% with 25% of fraction of inspired oxygen (FiO2) - (possibly nasal cannula inserted).

Exclusion Criteria:

  • Patients with low glasgow coma scale (GCS) score (less than 15).
  • Patients having inspiratory capacity of 3500ml and above.
  • Patients on ventilator.

Sites / Locations

  • Rehman Medical Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional Treatment

Scapular Mobilization

Arm Description

Thrice a day ,Conventional treatment according to American Heart Association Guidelines i.e., Incentive spirometer, chest clearance, expectoration of the sputum (suctioning if needed), mobilizing the patient out of bed, AAROM and AROM exercises.

Thrice a day Scapular mobilization (SM) along with Conventional treatment

Outcomes

Primary Outcome Measures

Incentive Spirometer
An incentive spirometer is a device that will expand the lungs by helping the patient breathe more deeply and fully
Borg scale
The Borg Rating of Perceived Exertion (RPE) is a way of measuring physical activity intensity level.
Numeric pain rating scale
What is a numerical pain rating scale? The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain
Digital Spirometer
Spirometer is a portable lung function testing device, which mainly used to examine lung function related parameters for patients

Secondary Outcome Measures

Full Information

First Posted
March 8, 2022
Last Updated
August 31, 2023
Sponsor
Riphah International University
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1. Study Identification

Unique Protocol Identification Number
NCT05285865
Brief Title
Scapular Mobilization on Inspiratory Capacity of Post-CABG Patients
Official Title
Effects of Scapular Mobilization on Inspiratory Capacity of Post-CABG Patients
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
March 15, 2022 (Actual)
Primary Completion Date
February 10, 2023 (Actual)
Study Completion Date
July 1, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Riphah International University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To determine the effects of scapular mobilization on pulmonary functions of post-CABG patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
CABG

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Conventional Treatment
Arm Type
Active Comparator
Arm Description
Thrice a day ,Conventional treatment according to American Heart Association Guidelines i.e., Incentive spirometer, chest clearance, expectoration of the sputum (suctioning if needed), mobilizing the patient out of bed, AAROM and AROM exercises.
Arm Title
Scapular Mobilization
Arm Type
Experimental
Arm Description
Thrice a day Scapular mobilization (SM) along with Conventional treatment
Intervention Type
Other
Intervention Name(s)
Conventional Treatment
Intervention Description
Thrice a day for complete length of stay. This is Conventional treatment The total duration of session will be of 15-20 mins.
Intervention Type
Other
Intervention Name(s)
Scapular Mobilization
Intervention Description
Thrice a day for complete length of stay including two sets of repetitions with a rest interval of 30 seconds between sets. Grade 1-3 As reported in a study Scapular mobilization (SM) i.e., Scapular superior, inferior glides, upward and downward rotations and scapular distraction, along with Conventional treatment according to American Heart Association Guidelines i.e., Incentive spirometer, chest clearance, expectoration of the sputum (suctioning if needed), mobilizing the patient out of bed, AAROM and AROM exercises.
Primary Outcome Measure Information:
Title
Incentive Spirometer
Description
An incentive spirometer is a device that will expand the lungs by helping the patient breathe more deeply and fully
Time Frame
1 week
Title
Borg scale
Description
The Borg Rating of Perceived Exertion (RPE) is a way of measuring physical activity intensity level.
Time Frame
1 week
Title
Numeric pain rating scale
Description
What is a numerical pain rating scale? The Numerical Pain Rating Scale (NPRS) is a subjective measure in which individuals rate their pain
Time Frame
1 week
Title
Digital Spirometer
Description
Spirometer is a portable lung function testing device, which mainly used to examine lung function related parameters for patients
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: CAD patients undergone CABG surgery (Post-Op. Day#. 01). Both genders (male and female). Aged between 40 to 70 years . Patient having oxygen saturation (SPO2) of more than or equal to 90% with 25% of fraction of inspired oxygen (FiO2) - (possibly nasal cannula inserted). Exclusion Criteria: Patients with low glasgow coma scale (GCS) score (less than 15). Patients having inspiratory capacity of 3500ml and above. Patients on ventilator.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Malik Muhammad Ali Awan, MSPT
Organizational Affiliation
Riphah International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rehman Medical Institute
City
Peshawar
State/Province
KPK
ZIP/Postal Code
46000
Country
Pakistan

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Scapular Mobilization on Inspiratory Capacity of Post-CABG Patients

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