- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05932147
Pilates Exercise Versus Manual Lymphatic Drainage On Axillary Web Syndrome Post Mastectomy
1-Subjects: Sixty-eight patients sample size according to G power who have Axillary web syndrome post mastectomy participated in this study. Their ages ranged from 35 to 55 years. The participants selected from learning hospitals (Al kasr Al Ayni hospital and National cancer institute) and randomly distributed into 2 equal groups.
1.1 Design of study: In this study the patients randomly assigned into two equal groups (34 patients for each group) 1.1(a) Group A: (Pilates Exercise)
1.1(b) Group B: (Manual Lymphatic Drainage)
2. Equipment's and Tools: Equipment in this study divided into two main categories: measuring and therapeutic equipment.
2.1. Measuring Equipment:
The following tools are used to assess Range of motion and pain for shoulder joint:
2.1 (a) Measuring and assessment of pain by:
- Visual analogue scale 2.2 (b) Measuring range of motion (ROM) by:
- Electronic Goniometer 2.3 (c) Measuring Disability of the arm, shoulder and hand by:
- DASH questionnaire (Disability of the arm, shoulder and hand). 2.2. Therapeutic Equipment: 1. Pilates exercise 2- Manual lymphatic drainage 3. Procedures of the study:
The procedures of this study are classified into the following:
3.1 Measurement Procedures: All measurements have been taken before treatment (pre) after 9 weeks (post 1) after 9 weeks (post 2).
1.1 (a) Assessment of pain of shoulder joint
• Assessment of upper limb pain using visual analogue scale 3.1(b) Assessment of Range of motion of shoulder joint: By Electronic Goniometer. 3.1 (c) Assessment of Disability of the arm, shoulder and hand The disabilities of the arm, shoulder and hand questionnaire (DASH) 1.2 Therapeutic procedures: 3.2(a) procedures of Pilates exercise program:
- Shoulder Abduction with External Rotation exercise
- Shoulder bridge exercise
- Mermaid sitting exercise.
- Standing Pilates mermaid exercise with towel
- Rocking exercise
- Saw Pilates exercise.
- Bird-dog Pilates exercise.
- Roll up exercise.
- Cobra pose exercise.
- Child pose exercise.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
1-Subjects: Sixty-eight patients sample size according to G power who have Axillary web syndrome post mastectomy participated in this study. Their ages ranged from 35 to 55 years. The participants have been selected from learning hospitals (Al kasr Al Ayni hospital and National cancer institute) and randomly distributed into 2 equal groups.
1.1 Design of study: In this study the patients randomly assigned into two equal groups (34 patients for each group) 1.1(a) Group A: (Pilates Exercise) This group includes 34 patients who have axillary web syndrome received Pilates exercise with traditional physical therapy exercise program (strength, core stability, flexibility, muscle control, posture and breathing). Patients will receive 3 sessions per week for 8 weeks; time of session is 30 minutes.
1.1(b) Group B: (Manual Lymphatic Drainage) This group includes 34 patients who axillary web syndrome received Manual lymphatic drainage massage with traditional physical therapy exercise program (strength, core stability, flexibility, muscle control, posture and breathing). Patients received 3 sessions per week for 8 weeks; time of session is 30 minutes.
2. Equipment's and Tools: Equipment in this study divided into two main categories: measuring and therapeutic equipment.
2.1. Measuring Equipment:
The following tools are used to assess Range of motion and pain for shoulder joint:
2.1 (a) Measuring and assessment of pain by:
- Visual analogue scale 2.2 (b) Measuring range of motion (ROM) by:
- Electronic Goniometer 2.3 (c) Measuring Disability of the arm, shoulder and hand by:
- DASH questionnaire (Disability of the arm, shoulder and hand). 2.2. Therapeutic Equipment: 1. Pilates exercise
Parameters:
- Duration 30 minutes.
- Patient own choice with guidance.
- Suitable equipment chosen for specific situation.
- Measurement and follow up
- Three session per week
- For 9 weeks 2- Manual lymphatic drainage
Parameters:
- Duration 30 minutes.
- Patient own choice with guidance.
- Suitable equipment chosen for specific situation.
- Measurement and follow up
- Three session per week
- For 9 weeks 3. Procedures of the study:
The procedures of this study are classified into the following:
3.1 Measurement Procedures: All measurements have been taken before treatment (pre) after 9 weeks (post 1) after 9 weeks (post 2).
1.1 (a) Assessment of pain of shoulder joint
- Assessment of upper limb pain using visual analogue scale
- VAS will be used to assess the degree of pain intensity subjectively by same subject. This scale consists of 10cm line with the words "No Pain" on the right side.
3.1(b) Assessment of Range of motion of shoulder joint: By Electronic Goniometer.
A standardized means of measuring and recording and a goniometer is aligned over a joint and with a click of a button the ROM measurement is entered automatically into E-LINK computer software, generating progress reports that can be utilized as definitive outcome measures. Goniometer to obtain goniometric measurements for shoulder flexion, abduction and external rotation will be used.
- Measuring of shoulder flexion range while patient is in supine position
- Measuring of shoulder abduction range while patient in sitting or supine position.
- Measuring of shoulder external rotation range while patient in supine position. 3.1 (c) Assessment of Disability of the arm, shoulder and hand The disabilities of the arm, shoulder and hand questionnaire (DASH)
- The disabilities of the arm, shoulder and hand (DASH) questionnaire is a self-administered region-specific outcome instrument developed as a measure of self-rated upper-extremity disability and symptoms.
The DASH consists mainly of a 30-item disability/symptom scale, scored 0 (no disability) to 100 1.2 Therapeutic procedures: 3.2(a) procedures of Pilates exercise program:
- Shoulder Abduction with External Rotation exercise
- Shoulder bridge exercise
- Mermaid sitting exercise.
- Standing Pilates mermaid exercise with towel
- Rocking exercise
- Saw Pilates exercise.
- Bird-dog Pilates exercise.
- Roll up exercise.
- Cobra pose exercise.
- Child pose exercise.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Dokki, Egypt
- Cairo university of physical therapy
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
• Age range between 35-55 years.
- Number of dissection of lymph nodes.
- No change of arm size.
- Females only will participate in the study.
- All patients have axillary web syndrome
- All patients' relatives enrolled to the study will have their informed consent
Exclusion Criteria:
• Age more than 55 years or less than 35 years.
- Lymphedema.
- Chemotherapy and Radiotherapy.
- Pregnant women.
- Patients who suffer from mental or psychological problems.
- Patients who have psoriasis, liver disease, diabetes mellitus, hypertensive patients and cardiac problems
- Patients have Genetic disease or deformity
- Who has previous injury or fracture in shoulder joint
- Rheumatoid arthritis
- Osteopenia
- Frozen shoulder
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Pilates group
This group includes 34 patients who have axillary web syndrome will receive Pilates exercise with traditional physical therapy exercise program (strength, core stability, flexibility, muscle control, posture and breathing).
Patients will receive 3 sessions per week for 9 weeks; time of session is 30 minutes.
|
|
|
Experimental: Manual lymphatic massage group
This group includes 34 patients who axillary web syndrome will receive Manual lymphatic drainage massage with traditional physical therapy exercise program (strength, core stability, flexibility, muscle control, posture and breathing).
Patients will receive 3 sessions per week for 9 weeks; time of session is 30 minutes.
|
procedures of Manual lymphatic drainage program Things to know about MLD Massage
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Electric Goniometer
Time Frame: 9 weeks
|
for RANGE OF MOTION MEASURMENT
|
9 weeks
|
|
DASH SCALE (Disability of arm, shoulder and hand)
Time Frame: 9 weeks
|
for disability measurement
|
9 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Prof. Dr. Haidy N Asham, Professor of Physical Therapy for Surgery
- Study Director: Ass. Prof. Dr. Ereny S Wahba Khalil, Assistant professor of Physical Therapy for Surgery
- Principal Investigator: Prof. Dr. Mohamed A Hassan Abolkasem, Professor of Clinical Oncology
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- P.T.REC/012/003745
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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