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The effect of mobile phone self-management program on the quality of life and lymphedema after breast cancer surgery

Clinical trial of the effectiveness of a mobile phone-based self-management program on the women's quality of life and lymphedema after breast cancer surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220927056047N1
Enrollment
180
Registered
2022-12-10
Start date
2022-12-22
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Condition 1: Breast cancer. Condition 2: Lymphedema. Malignant neoplasm of breast Postmastectomy lymphedema syndrome

Interventions

Intervention 1: Intervention group: In addition to the usual lymph clinic trainings and treatments, they will also receive a mobile-based self-management program. The program has sections including ed

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Have undergone breast cancer surgery along with axillary lymph node dissection A minimum time interval of 6 months between breast cancer surgery and entry in to the study Having literacy to read the educational content of the software Access to a mobile phone with the Android operating system (the patient herself or a family member) and the ability to use it Absence of mental disorders according to the patient's self report

Exclusion criteria

Exclusion criteria: Active malignancy Recurrence of breast cancer Patients undergoing chemotherapy and radiotherapy History of previous treatment of lymphedema Neuromuscular diseases, especially in the hand area Patients with high blood pressure and heart and kidney diseases Unwillingness to participate in the study

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: Before the intervention, 12 weeks after the start of the intervention. Method of measurement: Lymphedema life impact scale.;Lymphedema. Timepoint: Before the intervention, 12 weeks after the start of the intervention. Method of measurement: Measuring the circumference of the arms using a meter and entering in the arm circumference registration form.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrvash Hemati

Shiraz University of Medical Sciences

mehrvashhemati@sums.ac.ir+98 71 3647 4254

Outcome results

None listed

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