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Effect of 12 sessions of lymphatic message and Pilates training on lymph edema volume, anxiety, stress and depression, of life, and pain of 30-60 year-old breast cancer survivors

Effect of 12 sessions of lymphatic message and Pilates training on lymph edema volume, anxiety, stress and depression, of life, and pain of 30-60 year-old breast cancer survivors

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190202042581N6
Enrollment
75
Registered
2024-10-23
Start date
2024-09-22
Completion date
Unknown
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast cancer. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention group: Pilates exercises and lymphatic massage are performed daily for 5 days a week and up to 12 sessions. Intervention 2: Intervention group: Pilates exercises are perfo

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Having stage 2 and 3 breast cancer Adjuvant treatment with hormone therapy

Exclusion criteria

Exclusion criteria: Bilateral mastectomy advanced cancer

Design outcomes

Primary

MeasureTime frame
Pain severity. Timepoint: First session (before intervention), and 16 day (after intervention). Method of measurement: Visual Analogue Scale.;Lymphedema volume. Timepoint: First session (before intervention), and 16 day (after intervention). Method of measurement: Tape measure.;Arm range of motion. Timepoint: First session (before intervention), and 16 day (after intervention). Method of measurement: Goniometer.;Perceived stress. Timepoint: First session (before intervention), and 16 day (after intervention). Method of measurement: perceived stress scale (PSS) questionnaire.

Secondary

MeasureTime frame
Depression and anxiety. Timepoint: First session (before intervention), and 16 day (after intervention). Method of measurement: HADS questionnaire.;Quality of life. Timepoint: First session (before intervention), and 16 day (after intervention). Method of measurement: Quality of life questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSolmaz Rahbar

Hamedan University of Medical Sciences

s.rahbar@umsha.ac.ir+98 81 3838 1633

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026