- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05497869
Effects of Active Release Technique (ART) on Pectoralis Minor Tightness in Post Mastectomy Women.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Breast cancer may be a malignant neoplasm, an abnormal growth (carcinoma) originated in breast tissue that invade the encompassing tissue, grows infiltrative and destructive, and may metastasize.It is outlined pathologically by location of origin within the breast (e.g. ducts, lobes), size of the tumor, standing of the nodes, and also the presence of markers indicating tumor staging. Mostly, early-stage breast cancer diagnosed in women undergo surgical procedures, nearly half withstand breast-conserving surgery and one third experience mastectomy.
It is generally believed that physiotherapy aims to aid recovery and prevent complications following mastectomy however no well-designed, randomized controlled trial has investigated the effect of active release technique (ART) specifically on pectoralis minor in post-operative breast cancer women. Hence, a physiotherapy rehabilitation plan of care consisting of patient education, early mobilization along Active Release Technique (ART) may prevent postoperative complications like chest tightness and reduced shoulder mobility. This will enhance muscular relaxation, improve restricted mobility, and will result in improved quality of life as compared to standard care or conventional treatment alone.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Capital
-
Islamabad, Capital, Pakistan, 46000
- Federal Breast Cancer Screening center (PIMS)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- women complaining chest tightness
- Mastectomy (Unilateral/ Bilateral/ Partial/ Radical)
- Postoperative chemotherapy or radiation therapy
Exclusion Criteria:
- Tumor Metastasis with other tissue/ organ.
- Underlying Cardiac issues.
- Shoulder joint pathology before surgery.
- Post mastectomy pain syndrome (Pain beyond 3 months).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental interventional group
Active Release Technique (ART)
|
Patient is in supine lying position with 15-20° shoulder abduction.
Then place finger tips under Pectoralis minor tendon and position the arm in 90°/90° shoulder abduction and elbow flexion.
Apply the pressure while stroking the tender area and ask the patient to adduct the arm then bring shoulder backward while maintain the pressure 3 sets of 10 repetition/ 4 days per week for 3 weeks.
|
|
Active Comparator: active control group
conventional group
|
Conventional treatment- includes gentle shoulder ROMs i.e. flexion, extension, abduction, adduction, internal rotation and external rotation with-in pain free range, 10 repetitions each for 3 times a day
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
NPRS
Time Frame: 3rd week
|
Shoulder/Arm pain will assessed using a numerical pain rating scale (NPRS), and scoring range 0, no pain, to 10, maximum pain.
pain will be measure from baseline to 1st week to 2nd and 3rd week
|
3rd week
|
|
Shoulder Pain and Disability Index (SPADI)
Time Frame: 3rd week
|
The SPADI is a valid and reliable 13-item shoulder specific instrument measuring both shoulder disability and pain which is divided into two subscales: pain (5 items) and disability (8 items).
Scores on both subscales are rated from 0 (no pain or disability) to 10 (worst pain imaginable or so difficult to perform tasks that help is required).
The SPADI has proven to be a reliable, valid, and sensitive instrument.
Total SPADI score, (0-130), in which, (0-29= little or no pain/disability), (30-49= Mild to moderate pain/disability), (50-130= Moderate to severe pain/disability) It will be measure from baseline to 1st week to 2nd and 3rd week
|
3rd week
|
|
pectoralis minor length through vernier caliper
Time Frame: 3rd week
|
it will be measure from baseline to 1st week to 2nd and 3rd week.
Vernier® caliper (intraclass correlation coefficient 0.83-0.87) is used to measure pectoralis minor length.
The patients were in the supine position with a normal, relaxed posture.
The caliper arms were placed between the coracoid processes to the fourth rib 1-finger apart from lateral to the sternum.
As 2.6 cm or 1inch distance has been proposed as the normal length of pectoralis minor muscle
|
3rd week
|
|
pectoralis minor length through Rigid standard plastic transparent right angle
Time Frame: 3rd week
|
it will be measure from baseline to 1st week to 2nd and 3rd week.
This tool used to measure the linear distance in millimeter from the table to the posterior acromion of the patients in supine position with the arms by the side and elbows in flexed and rested on abdomen.
Without adding any pressure on the table, the base of the protractor was placed on the bed and the vertical side was placed posterior to the acromion
|
3rd week
|
Collaborators and Investigators
Sponsor
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
- RiphahIU Shafaq
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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.
Clinical Trials on Postgastrectomy Syndrome
-
Radboud University Medical CenterUnknown
-
Universitaire Ziekenhuizen KU LeuvenIpsenCompleted
-
Novartis PharmaceuticalsCompletedDumping SyndromeBelgium, Netherlands, Germany, France, United States
-
Technological Educational Institute of ThessalyRecruiting
-
Larissa University HospitalRecruitingDumping Syndrome | Gastric SurgeryGreece
-
Samsung Medical CenterRecruitingDumping Syndrome | Esophagectomy | Continous Glucose MeasurementSouth Korea
-
Instituto Mexicano del Seguro SocialRecruitingGastroesophageal Reflux | Postgastrectomy SyndromesMexico
-
Universitaire Ziekenhuizen KU LeuvenCompletedPostoperative Dumping SyndromeBelgium
-
University Hospital, LilleCompleted
-
Mina Kamal Gergis ErianKasr El Aini HospitalActive, not recruitingMetabolic Diseases | Quality of Life | Obesity | Nutritional Status | Morbid Obesity | Bariatric Surgery | Dumping Syndrome | Sleeve Gastrectomy | Postgastrectomy Syndrome | Patient-reported Outcome Measures | Gastrointestinal Function Disorders | Gastrointestinal TransitEgypt
Clinical Trials on active release group
-
Riphah International UniversityCompletedLateral EpicondylitisPakistan
-
Riphah International UniversityCompletedKnee OsteoarthritisPakistan
-
Lahore University of Biological and Applied SciencesNot yet recruiting
-
Canadian Memorial Chiropractic CollegeCompleted
-
University of LahoreCompletedHamstring Shortening, Short Hamstring SyndromePakistan
-
Riphah International UniversityNot yet recruitingTension-Type HeadachePakistan
-
Riphah International UniversityRecruitingPain | Gait | Plantar FascitisPakistan
-
Shin Kong Wu Ho-Su Memorial HospitalRecruitingCarpal Tunnel Syndrome | Ultrasound | Carpal Tunnel Release | Dextrose | Nerve Hydrodissection TherapyTaiwan
-
Sehat Medical ComplexCompletedPiriformis SyndromePakistan
-
Logan College of ChiropracticUnknownTemporomandibular Joint Dysfunction Syndrome | Temporomandibular Joint Disorder | Temporomandibular JointUnited States