Scapular Mobilization and Proprioceptive Neuromuscular Facilitation on Shoulder Dysfunction After Latissimus Dorsi Flap Breast Reconstruction
PNF
1 other identifier
interventional
36
0 countries
N/A
Brief Summary
this study will be conducted to investigate the effect of scapular mobilization and scapular Proprioceptive neuromuscular facilitation on shoulder dysfunction after latissimus dorsi flap breast reconstruction
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 17, 2026
CompletedFirst Posted
Study publicly available on registry
April 23, 2026
CompletedStudy Start
First participant enrolled
April 25, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
April 23, 2026
April 1, 2026
4 months
April 17, 2026
April 17, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
pain intensity
The Visual analogue Scale (VAS) will be used for the measurement of pain. It consists of a line usually 100 mm in length, with anchor descriptors such as (in the pain context) "no pain" and "worst pain imaginable"
up to eight weeks
shoulder and arm disability
Disability of the arm, shoulder and hand questionnaire will be used to assess shoulder and arm disability. This system gives a percentage disability score of upper limbs where 0 indicates no disability and 100 indicates complete disability. The DASH questionnaire consists of 30 questions assessing the impact of upper limb disability (if any) on activities of daily living. There are also optional sections within the questionnaire examining the effect of their limb function at the work place during sports or when playing musical instruments
up to eight weeks
Secondary Outcomes (3)
shoulder range of motion
up to eight weeks
scapular upward rotation
up to eight weeks
scapular downward rotation
up to eight weeks
Study Arms (2)
scapular mobilization and scapular proprioceptive neuromuscular facilitation exercises
EXPERIMENTALeighteen female patients suffering from shoulder dysfunction after latissimus dorsi flap breast reconstruction. They received scapular mobilization and scapular PNF three session per week for 8 weeks in addition to the traditional physical therapy program.
traditional physical therapy
ACTIVE COMPARATOReighteen female patients suffering from shoulder dysfunction after latissimus dorsi flap breast reconstruction. They received a traditional physical therapy program, three sessions per week for eight weeks.
Interventions
the patients will recieve the traditional physical therapy program in the form of shoulder Range of motion, stretching and strengthening exercises.
for scapular mobilization, The patient will be laying on the affected forearm on their back. The therapist is standing before the patient's affected shoulder, placing the index finger of one hand under the medial scapular border, the other hand grasping the superior border of the scapula. The scapula was moved superiorly and inferiorly for superior and inferior glide, and then the scapula is rotated upward and downward for scapular rotation. Second, with the patient was in the same position the physiotherapist put the ulnar fingers under the medial scapular border and distracted the scapula from the thorax. Sets of 10 repetitions were applied performed at a rate of one cycle per 6 s, with a rest interval of 30 seconds between sets. for PNF is applied by a trained therapist in two diagonals, anterior elevation and posterior depression and posterior elevation and anterior depression with 20 repetitions for each diagonal. plus tradional physical therapy.
Eligibility Criteria
You may qualify if:
- age ranged from 40 to 55 years.
- All patients were female patients suffering from shoulder dysfunction after latissimus dorsi flap breast reconstruction.
- All patients suffering from moderate or severe pain on shoulder joint and limited range of motion that may affect daily activities.
- All patients begun the treatment program 3 to 4 weeks after LDF breast reconstruction.
- Informed consent was obtained from every patient enrolled in the trial.
You may not qualify if:
- Current metastases.
- Neurological deficit affecting the shoulder functioning during daily activities.
- Pathology of the shoulder joint including rotator cuff tear adhesive capsulitis and tendinitis.
- Pain or disorder of the cervical spine, elbow, wrist or hand.
- Shoulder surgery, shoulder dislocation fracture acromioclavicular joint osteoarthritis.
- Diabetes.
- Pregnancy.
- Shoulder manipulation under anesthesia, local corticosteroid injection.
- Psychological disorders.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- opaque sealed envelope
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principle investigator : Madonna Magdy Isaac Ibrahim
Study Record Dates
First Submitted
April 17, 2026
First Posted
April 23, 2026
Study Start
April 25, 2026
Primary Completion (Estimated)
September 1, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
April 23, 2026
Record last verified: 2026-04