Effect of Kinetic Control Exercise on Shoulder Dysfunction Post Mastectomy

NCT ID: NCT07023913

Last Updated: 2025-06-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-15

Study Completion Date

2025-10-15

Brief Summary

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The purpose of this study is to evaluate the effect of kinetic control exercises on shoulder dysfunction in post-mastectomy.

Detailed Description

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This study holds significant importance for clinical practice, patient care, and research.

* Clinical Practice: It provides a potential framework for physical therapists to design targeted and effective interventions for shoulder dysfunction in post-mastectomy patients.
* Patient Care: Improved rehabilitation outcomes can enhance patients' physical functionality, independence, and overall quality of life, addressing a critical gap in post-operative recovery.
* Research Advancement: By contributing to the limited body of literature on kinetic control in this context, the study can stimulate further research and innovation in rehabilitative care for breast cancer survivors.

Conditions

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Kinetic Control Dysfunction Shoulder Mastectomy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Kinetic Control Exercise

This group includes 30 patients who had mastectomy and will receive Kinetic control exercise inform of activation local and general Stabilizer, mobilizer), and traditional exercise. Patients will receive 3 sessions per week for 8 weeks.

Group Type EXPERIMENTAL

kinetic Control exercises

Intervention Type OTHER

Kinetic Control exercises consist of 45-minute sessions, with 3 sessions per week for 8 weeks. The framework for testing and rehabilitation includes initial assessment, rehabilitation before failure, and retesting the same position. Biofeedback measures scapular retraction, and biofeedback pressure training assesses and improves scapular stabilizer control by monitoring pressure changes during specific movements.

traditional treatment

Intervention Type OTHER

traditional therapy inform of stretching and strengthening exercise as shoulder roll, arm circle, wall climb, back climb and hand behind neck. Patients will receive 3 sessions per week for 8 weeks, the time of session is 45 - 60 min according to patient ability

traditional therapy

This group includes 30 patients who have undergone mastectomy and will receive traditional therapy inform of stretching and strengthening exercise as shoulder roll, arm circle, wall climb, back climb and hand behind neck. Patients will receive 3 sessions per week for 8 weeks.

Group Type ACTIVE_COMPARATOR

traditional treatment

Intervention Type OTHER

traditional therapy inform of stretching and strengthening exercise as shoulder roll, arm circle, wall climb, back climb and hand behind neck. Patients will receive 3 sessions per week for 8 weeks, the time of session is 45 - 60 min according to patient ability

Interventions

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kinetic Control exercises

Kinetic Control exercises consist of 45-minute sessions, with 3 sessions per week for 8 weeks. The framework for testing and rehabilitation includes initial assessment, rehabilitation before failure, and retesting the same position. Biofeedback measures scapular retraction, and biofeedback pressure training assesses and improves scapular stabilizer control by monitoring pressure changes during specific movements.

Intervention Type OTHER

traditional treatment

traditional therapy inform of stretching and strengthening exercise as shoulder roll, arm circle, wall climb, back climb and hand behind neck. Patients will receive 3 sessions per week for 8 weeks, the time of session is 45 - 60 min according to patient ability

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

The subject selection will be according to the following criteria:

* Age from 40 to 50 years.
* All patients have no diabetes or blood problems.
* All patients enrolled to the study will have their informed consent.

Exclusion Criteria

The potential participants will be excluded if they meet one of the following criteria:

* Age less than 40 or more 50 years.
* Diabetes mellitus.
* Subjects with lymphedema
* Subjects suffering from active malignant tumors.
* Subjects treated with skin graft.
* Subjects with Mental illness.
* Subjects with skin diseases
* Subjects with any previous cause for shoulder dysfunction
Minimum Eligible Age

40 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Alaa Tarek Mostafa ElNawawy

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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learning hospitals Al Kaser Al Ayni hospital

Cairo, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Alaa Tarek Mostafa Elnawawy, physical therapist

Role: CONTACT

+201005730916

Facility Contacts

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Alaa Tarek Mostafa Elnawawy, physical therapist

Role: primary

+201005730916

Other Identifiers

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Alaa-005696

Identifier Type: -

Identifier Source: org_study_id

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