- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05911867
Muscle Energy Technique and Mulligan's Mobilization in Breast Cancer Surgery Patients (MWMMET)
The Combined Effect of Mulligan and Muscle Energy Techniques on Shoulder Kinematics and Postural Changes After Breast Cancer Surgery With Axillary Dissection: A Prospective, Randomized, Controlled Clinical Trial
Study Overview
Status
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Hany M Elgohary, Ph.D
- Phone Number: 00201093182291
- Email: hmielgohary@gmail.com
Study Contact Backup
- Name: Alaa M Khedr
- Phone Number: 00201555001550
- Email: alaa.wageeh25@gmail.com
Study Locations
-
-
-
Cairo, Egypt, 11432
- Recruiting
- Hany Mohamed Elgohary
-
Contact:
- Hany M Elgohary, PhD
- Phone Number: 0590997821
- Email: gohary75pt@hotmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- female
- between 50 and 65 years
- limited shoulder range of motion
Exclusion Criteria:
- having metastases
- lymphedema
- traumatic or musculoskeletal disorders affecting the arm
- not taking anticoagulants
- not having undergone bilateral breast cancer surgery
- not having a locoregional recurrence
- not having vascular disorders in the affected arm
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: combination of mobilization with movement and muscle energy techniques
Mulligan technique (MWM) involves the therapist using a belt around the humeral head to guide appropriate gliding while the patient moves their shoulder actively through the range. The therapist applies pressure to the scapula in a counter direction. Regarding the cervical spine, the second technique, Cervical Self-Natural Apophyseal Glides (SNAG), involves the therapist standing behind the patient and applying force to the spinous process of each vertebra using a thumb-over-thumb technique. The examiner passively abducts the arm in the horizontal plane until the first barrier to motion by applying pressure to the distal humerus. This passive stretch will be held for three seconds. |
The examiner passively abducts the arm in the horizontal plane until the first barrier to motion by applying pressure to the distal humerus. The participant then actively abduct the arm in the horizontal plane for a three-second active-assisted stretch. Regarding the cervical spine, the second technique, Cervical Self-Natural Apophyseal Glides (SNAG), involves the therapist standing behind the patient and applying force to the spinous process of each vertebra using a thumb-over-thumb technique. The patient actively performs repeated flexion or extension of their neck, returning back to the neutral position. The passive gliding is maintained in the anterosuperior direction along the facet joint line while flexing or extending the neck throughout the range.
Other Names:
|
|
Active Comparator: mobilization with movement
Regarding the shoulder joint, the Mulligan technique (MWM) involves the therapist using a belt around the humeral head to guide appropriate gliding while the patient moves their shoulder actively through the range. The therapist applies pressure to the scapula in a counter direction. This technique is usually performed for five sets of five repetitions with one minute of rest between sets in a sitting position. Regarding the cervical spine, the second technique, Cervical Self-Natural Apophyseal Glides (SNAG), involves the therapist standing behind the patient and applying force to the spinous process of each vertebra using a thumb-over-thumb technique. The patient actively performs repeated flexion or extension of their neck, returning back to the neutral position. |
Regarding the cervical spine, the second technique, Cervical Self-Natural Apophyseal Glides (SNAG), involves the therapist standing behind the patient and applying force to the spinous process of each vertebra using a thumb-over-thumb technique.
The patient actively performs repeated flexion or extension of their neck, returning back to the neutral position.
The passive gliding is maintained in the anterosuperior direction along the facet joint line while flexing or extending the neck throughout the range.
|
|
Active Comparator: muscle energy techniques
The examiner passively abduct the arm in the horizontal plane until the first barrier to motion by applying pressure to the distal humerus.
This passive stretch will be held for three seconds.
The examiner then instruct the participant to attempt to horizontally adduct the test arm at 25% of their maximal effort while the examiner applies manual resistance at the distal humerus to create an isometric contraction lasting five seconds.
The participant then actively abduct the arm in the horizontal plane for a three-second active-assisted stretch.
|
The examiner passively abduct the arm in the horizontal plane until the first barrier to motion by applying pressure to the distal humerus.
This passive stretch will be held for three seconds.
The examiner then instruct the participant to attempt to horizontally adduct the test arm at 25% of their maximal effort while the examiner applied manual resistance at the distal humerus to create an isometric contraction lasting five seconds.
The participant then actively abduct the arm in the horizontal plane for a three-second active-assisted stretch.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
digital inclinometer
Time Frame: 6 weeks
|
).
This tool is recognized as valid and reliable for this purpose and requires the patient to move their affected shoulder in various directions while keeping their feet fixed in place
|
6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postural Assessment Software (PAS/SAPO)
Time Frame: 6 weeks
|
The women participants were positioned in a comfortable stance, and anatomical markers will be attached to specific points such as the tragus and both acromions.
Their photographs will be captured and later analyzed using the PAS/SAPO software to record the cervical angle and horizontal alignment of the acromions.
A forward head position was identified by an angle less than 50°.
This method has been demonstrated to be reliable and valid for identifying forward head positions
|
6 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quick DASH scale
Time Frame: 6 weeks
|
The Arabic version of the Quick-DASH questionnaire includes 11 items, which inquire about the patient's difficulty in performing physical activities related to the upper extremity, the severity of pain and tingling, and the impact of the problem on social activities, work, and sleep.
Each item includes five response options, ranging from no difficulty to being unable to perform the activity.
If at least 10 items are answered, their responses are added to create a raw score, which is then transformed to a 0-100 scale.
|
6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Hany M Elgohary, Delta University for Science and Technology, Gamasa, Coastal Road
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- F.P.T2207005
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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