CABGNCT05285865
Scapular Mobilization on Inspiratory Capacity of Post-CABG Patients
A study testing Conventional Treatment and Scapular Mobilization in people with CABG, run by Riphah International University at 1 site in Pakistan.
Trial summary
To determine the effects of scapular mobilization on pulmonary functions of post-CABG patients. Read more about this study
- Who is it for?
- Ages 40 to 70 years
- Conditions the study is for
- CABG
- What is being tested?
- Conventional Treatment and Scapular Mobilization
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 40 participants
- Where
- 1 sitePakistan
- Study dates
- 15 Mar 2022to 1 Jul 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 40 to 70 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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).
Who cannot join
- Patients with low glasgow coma scale (GCS) score (less than 15).
- Patients having inspiratory capacity of 3500ml and above.
- Patients on ventilator.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effects of Scapular Mobilization on Inspiratory Capacity of Post-CABG Patients
To determine the effects of scapular mobilization on pulmonary functions of post-CABG patients.
- Conditions
- CABG
- Being tested
- Conventional Treatment, Scapular Mobilization
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Conventional TreatmentOther
Thrice a day for complete length of stay. This is Conventional treatment The total duration of session will be of 15-20 mins.
Scapular MobilizationOther
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.
| Study group | Role | What they receive |
|---|---|---|
| Conventional Treatment | Active comparator | 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. Receives: Other: Conventional Treatment |
| Scapular Mobilization | Experimental | Thrice a day Scapular mobilization (SM) along with Conventional treatment Receives: Other: Scapular Mobilization |
What is being measured
The primary outcome is the main question the study is designed to answer.
Incentive Spirometer
An incentive spirometer is a device that will expand the lungs by helping the patient breathe more deeply and fully
Measured: 1 week
Borg scale
The Borg Rating of Perceived Exertion (RPE) is a way of measuring physical activity intensity level.
Measured: 1 week
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
Measured: 1 week
Digital Spirometer
Spirometer is a portable lung function testing device, which mainly used to examine lung function related parameters for patients
Measured: 1 week
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Mar 2022
- Study start15 Mar 2022
- Primary completion10 Feb 2023
- Study completion1 Jul 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for CABGStudies of the same condition, open and under way.
- More trials run by Riphah International UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 40 participants (actual)
Sponsor and investigators
- Lead sponsor
- Riphah International University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Malik Muhammad Ali Awan, MSPT, Principal investigator, Riphah International University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05285865
- Sponsor's protocol ID
- REC/01278 Sakina Asghar
- Status last verified
- Aug 2023
- First submitted
- 8 Mar 2022
- Last updated
- 1 Sep 2023
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 1 Sep 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects of Scapular Mobilization on Inspiratory Capacity of Post-CABG Patients
- ClinicalTrials.gov ID
- NCT05285865
- Acronym / sponsor ID
- REC/01278 Sakina Asghar
- Conditions
- CABG
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 40 participants (actual)
- Lead sponsor
- Riphah International UniversityUniversity, hospital or other
- Study start
- 15 Mar 2022 (actual)
- Primary completion
- 10 Feb 2023 (actual)
- Study completion
- 1 Jul 2023 (actual)
- First posted
- 18 Mar 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To determine the effects of scapular mobilization on pulmonary functions of post-CABG patients.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Conventional Treatment | Active comparator | Other: Conventional TreatmentThrice 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. |
| Scapular Mobilization | Experimental | Other: Scapular MobilizationThrice a day Scapular mobilization (SM) along with Conventional treatment |
Who may qualify
- Ages
- 40 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- 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).
Key exclusion criteria (3 listed)
- Patients with low glasgow coma scale (GCS) score (less than 15).
- Patients having inspiratory capacity of 3500ml and above.
- Patients on ventilator.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Conventional TreatmentThrice a day for complete length of stay. This is Conventional treatment The total duration of session will be of 15-20 mins. | Other | Conventional Treatment |
| Scapular MobilizationThrice 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. | Other | Scapular Mobilization |
Primary outcome
Incentive Spirometer
Time frame: 1 week
An incentive spirometer is a device that will expand the lungs by helping the patient breathe more deeply and fully
Borg scale
Time frame: 1 week
The Borg Rating of Perceived Exertion (RPE) is a way of measuring physical activity intensity level.
Numeric pain rating scale
Time frame: 1 week
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
Time frame: 1 week
Spirometer is a portable lung function testing device, which mainly used to examine lung function related parameters for patients
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Sep 2023.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Malik Muhammad Ali Awan, MSPT principal investigator
Riphah International University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Conventional Treatment and Scapular Mobilization in people with CABG, run by Riphah International University at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Incentive Spirometer (time frame: 1 week). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Sep 2023.