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Effect of Digital Combined Decongestive Therapy in Patients With Breast Cancer-related Lymphedema: a Follow-up Study

B

Bezmialem Vakif University

Status

Completed

Conditions

Breast Cancer-Related Lymphedema

Treatments

Behavioral: Digital Combined Decongestive Therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT07014657
Lenfödemüst2025

Details and patient eligibility

About

This study investigated the short- and long-term effects of digital combined decongestive therapy in breast cancer-related lymphedema. Limb volume and quality of life (Lymph-ICF) were assessed at baseline, post-treatment, and 12-week follow-up.

Full description

This study evaluated the feasibility and effectiveness of a digital combined decongestive therapy (CDT) program in patients with breast cancer-related lymphedema. After an initial face-to-face training session on self-bandaging, self-manual lymphatic drainage, breathing exercises, and skin care, patients followed a 4-week digital CDT program with remote guidance. Compression garments were used during the maintenance phase. Limb volume was measured using circumference method. Quality of life was assessed with the Lymph-ICF questionnaire. Assessments were repeated post-treatment and at 12-week follow-up.

Enrollment

29 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with breast cancer-related lymphedema (BCRL) within the last 6 to 60 months.
  • Voluntarily agreed to participate in the study.

Exclusion criteria

  • Presence of active infection.
  • History of bilateral breast surgery.
  • Severe breast cancer-related lymphedema.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

29 participants in 1 patient group

Digital Combined Decongestive Therapy Group
Experimental group
Description:
Participants received digital combined decongestive therapy including self-bandaging, self-manual lymphatic drainage, decongestive and breathing exercises, supervised remotely through telecommunication technologies for 4 weeks, followed by maintenance therapy with compression stockings.
Treatment:
Behavioral: Digital Combined Decongestive Therapy

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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