Effectiveness of Scapular Clock Exercises in Scapular Dyskinesia in Post-Operative Open Heart Surgery Patients

Effectiveness of Scapular Clock Exercises in Scapular Dyskinesia; A Randomized Clinical Trial

In patients after open-heart surgery, the complaint of scapular dyskinesia is very common. It occurs due to the weakness of the muscles surrounding the scapula. In this research, investigators checked the effectiveness of scapular clock exercises in scapular dyskinesia, in post-op open heart surgery patients. There were two groups, an intervention "Active group" and a 'control group'. The patients will be randomly assigned to each group equally. The treatment session was given for a period of 4 weeks, with 3 sessions each week. They were assessed before treatment, after 2 weeks and post-intervention.

Study Overview

• Status: Recruiting
• Conditions: Scapular Dyskinesis
• Intervention / Treatment: Other: Scapular clock exercises; Other: Stretching and strengthening exercises

Detailed Description

Scapular dyskinesia is the malalignment of the scapula. It occurs when the pectoralis muscle (pectoralis minor) becomes tight and there is the weakness of the trapezius muscle (lower fibers). It can commonly occur after open-heart surgery due to incision and prolonged bed rest. In this research, the effectiveness of scapular clock exercises was checked. These exercises can strengthen the weak trapezius muscle and also stretch the tight pectoralis minor muscle. By adding these exercises in cardiac rehabilitation the occurrence of scapular dyskinesia can be reduced. Post-op open heart surgery patients mostly present with complain of shoulder pain. Most of their treatment is directed towards shoulder joint while the scapula is usually ignored. So it is important to add exercises directed towards the scapula along with shoulder.

In this study, The investigators will recruit 30 post-op cardiac surgery patients with complain of shoulder pain, with positive scapular dyskinesia. The sample size was calculated using formula and the values were taken from previous researches. Scapular assistance test and Scapular retraction test was used to find out patients with scapular dyskinesia. The subjects will then be randomly divided into two groups using online randomization generator. The interventional group was receive stretching and strengthening exercises with additional scapular clock exercises and the active control group will receive stretching and strengthening exercises. There was 3 sessions per week, for a period of 4 weeks. The patients was assessed prior to the treatment , then after 2 weeks and later after completion of 4 weeks. The tools for assessment include NPRS for pain, Quick-DASH for activity limitation of shoulder and goniometer for measuring range of motion of shoulder.

• Study Type: Interventional
• Enrollment (Anticipated): 30
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Aqsa Shahid, Doctor of Physical Therapy; Phone Number: 0301-8057342; Email: ladydocter48@gmail.com
• Study Contact Backup: Name: Sana Zahir, Doctor of Physical Therapy; Phone Number: 0306-6396683; Email: sanazahir22@gmail.com

Study Locations

• Pakistan
  • Punjab
    • Faisalābad, Punjab, Pakistan, 34000
      • Recruiting
      • Faisalabad institute of cardiology
      • Contact: Aqsa Shahid, Doctor of Physical Therapy; Phone Number: 0301-8057342; Email: ladydocter48@gmail.com
      • Contact: Sana Zahir, Doctor of Physical Therapy; Phone Number: 0306-6396683; Email: sanazahir22@gmail.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 31 years to 61 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Patients whose open heart surgery is done at least 6weeks ago.
• Subjects having shoulder and scapular region pain.
• 50% or less loss of Active ROM of shoulder in abduction, flexion and external rotation.
• Positive Scapular assistance (SAT) and Scapular retraction test.
• Positive findings on observational examination of scapula, showing abnormal prominence of either inferior, medial or superior border of scapula.
• Type I and Type II scapular dyskinesia present
• Consented to take part in the study.

Exclusion Criteria:

• • Bilateral shoulder involvement

  • History of previous surgery on shoulder
  • Shoulder fracture
  • Glenohumeral or acromioclavicular joint Arthritis.
  • Neuromuscular disorders

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Group A; The interventional group received stretching and strengthening exercises along with scapular clock exercises. For the first two weeks, only scapular clock exercises were performed by the patient actively. After 2 weeks, the subjects performed scapular clock exercises by using the thera-band.	Other: Scapular clock exercises; In scapular clock exercises, the hand is placed on the wall in front of your body. Move the hand in direction of 12 and 6 o'clock to elevate and depress the scapula. Then move hands towards 9 o' clock and 3 o'clock direction to protract and retract the scapula. Hold each position for 10 seconds. From 3rd week and onward the patient will use thera-band and then perform clock exercises.; Other Names: Stretching and strengthening exercises (Physical Therapy); Other: Stretching and strengthening exercises; Stretching and strengthening exercises of shoulder and scapular muscles was performed including wall washes, corner stretch, pectoral muscles stretch and wall push ups.
Active Comparator: Group B; The active control group received stretching and strengthening exercises only. The stretching and strengthening exercises include corner stretch, wall-washes and pectoralis minor muscle stretch.	Other: Stretching and strengthening exercises; Stretching and strengthening exercises of shoulder and scapular muscles was performed including wall washes, corner stretch, pectoral muscles stretch and wall push ups.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Shoulder pain	Shoulder pain was assessed by using the Numeric Pain Rating (NPRS) Scale. NPRS is an 11-item Likert scale having 0 as no pain and 10 as maximum pain	4 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Level of Shoulder activity limitation	The level of shoulder activity limitation was assessed by using the Quick-DASH questionnaire. There were 11 questions that were rated by the Likert scale having 1 as no disability and 5 as maximum disability	4 weeks

Other Outcome Measures

Outcome Measure	Measure Description	Time Frame
Shoulder Range of Motion (ROM)	Shoulder ROM will be assessed by using a Goniometer	4 weeks

Collaborators and Investigators

• Sponsor: University of Faisalabad
• Investigators: Principal Investigator: Izza Ayub, MS Physical Therapy, The University of Faisalabad

Study record dates

Study Major Dates

• Study Start (Actual): April 15, 2022
• Primary Completion (Anticipated): June 20, 2022
• Study Completion (Anticipated): June 30, 2022

Study Registration Dates

• First Submitted: May 25, 2022
• First Submitted That Met QC Criteria: June 20, 2022
• First Posted (Actual): June 22, 2022

Study Record Updates

• Last Update Posted (Actual): June 22, 2022
• Last Update Submitted That Met QC Criteria: June 20, 2022
• Last Verified: June 1, 2022

More Information

Terms related to this study

• Keywords: Open Heart Surgery; Scapular dyskinesia; Scapular Clock Exercises
• Additional Relevant MeSH Terms: Central Nervous System Diseases; Nervous System Diseases; Neurologic Manifestations; Movement Disorders; Dyskinesias
• Other Study ID Numbers: TUF/DR/DPT/366

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No