NCT07547982

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

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
4mo left

Started Apr 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress10%
Apr 2026Sep 2026

First Submitted

Initial submission to the registry

April 17, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 23, 2026

Completed
2 days until next milestone

Study Start

First participant enrolled

April 25, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Last Updated

April 23, 2026

Status Verified

April 1, 2026

Enrollment Period

4 months

First QC Date

April 17, 2026

Last Update Submit

April 17, 2026

Conditions

Keywords

Scapular MobilizationProprioceptive Neuromuscular FacilitationLatissimus Dorsi Flap Breast Reconstruction

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

EXPERIMENTAL

eighteen 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.

Other: scapular mobilization and scapular proprioceptive neuromuscular facilitation exercisesOther: traditional physical therapy

traditional physical therapy

ACTIVE COMPARATOR

eighteen 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.

Other: traditional physical therapy

Interventions

the patients will recieve the traditional physical therapy program in the form of shoulder Range of motion, stretching and strengthening exercises.

scapular mobilization and scapular proprioceptive neuromuscular facilitation exercisestraditional physical therapy

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.

scapular mobilization and scapular proprioceptive neuromuscular facilitation exercises

Eligibility Criteria

Age40 Years - 55 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsthis study depend on only female after mastectomy
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Central Study Contacts

madonna isaac, master

CONTACT

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
Model Details: scapular mobilization, scapular PNF and traditional physical therapy
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