Status:

NOT_YET_RECRUITING

Effectiveness of a Therapeutic Exercise Program With Specific Upper Limb Exercises to Reduce Lymphedema and Neuropathy in Breast Cancer Patients: A Pre-post Study (LYNMA)

Lead Sponsor:

Universitat Internacional de Catalunya

Collaborating Sponsors:

Consorci Sanitari de Terrassa

Conditions:

Lymphedema Arm

Lymphedema Due to Radiation

Eligibility:

FEMALE

35-70 years

Phase:

NA

Brief Summary

This study aims to evaluate the effectiveness of a therapeutic exercise program designed specifically for women with breast cancer. The program includes general exercises along with specific movements...

Detailed Description

This pre-post intervention study aims to assess the effectiveness of a comprehensive therapeutic exercise program tailored for breast cancer patients experiencing lymphedema and neuropathy secondary t...

Eligibility Criteria

Inclusion

  • Patients receiving treatment for breast carcinoma.reatments include surgical procedures (breast-conserving surgery or mastectomy), axillary lymph node dissection, sentinel lymph node biopsy, radiotherapy, chemotherapy, and hormone therapy.
  • Participants must provide authorization from their primary care physician and/or oncologist to perform therapeutic exercise.
  • Diagnosis of lymphedema associated with stage I or II breast cancer (Stage 1 or mild: circumference difference less than 4 cm \[volume difference 10-25%\] compared to the healthy arm; Stage 2 or moderate: circumference difference between 4 and 6 cm \[volume difference 25-50%\] compared to the healthy arm).
  • A score of 4 or higher on the DN4 questionnaire (neuropathic pain)

Exclusion

  • Lack of medical authorization.
  • Pre-existing cardiac pathology prior to cancer diagnosis.
  • Exacerbation of comorbidities.
  • Travel time exceeding 45 minutes to the location where the therapeutic exercise program is conducted.

Key Trial Info

Start Date :

January 1 2026

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 1 2026

Estimated Enrollment :

30 Patients enrolled

Trial Details

Trial ID

NCT07170631

Start Date

January 1 2026

End Date

October 1 2026

Last Update

September 18 2025

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