Effects of physiotherapy on sleep and quality of life in women with lymphedema after breast cancer

Investigation of the Effects of Complex Decongestive Physiotherapy on Sleep Quality and Quality of Life in Women With Breast Cancer Related Lymphedema

Not applicable Interventional Abant Izzet Baysal University · NCT06697158

This study is testing whether special physiotherapy can help women with lymphedema after breast cancer feel better and sleep more soundly.

Quick facts

PhaseNot applicable
Study typeInterventional
Enrollment31 (estimated)
Ages18 Years to 85 Years
SexFemale
SponsorAbant Izzet Baysal University Academic / other
Drugs / interventionschemotherapy
Locations2 sites (Bolu and 1 other locations)
Trial IDNCT06697158 on ClinicalTrials.gov

What this trial studies

This investigation focuses on the impact of complex decongestive physiotherapy on sleep quality and overall quality of life in women suffering from breast cancer-related lymphedema. The study aims to enroll participants aged 18 to 85 who have been diagnosed with unilateral stage 2 lymphedema following breast cancer surgery. Through targeted physiotherapy interventions, the study seeks to alleviate physical symptoms and improve psychosocial well-being, addressing issues such as swelling, pain, and sleep disturbances. The methodology includes comprehensive assessments of participants' sleep quality and quality of life before and after the intervention.

Who should consider this trial

Good fit: Ideal candidates for this study are women aged 18 to 85 with unilateral stage 2 lymphedema following breast cancer surgery.

Not a fit: Patients with bilateral lymphedema, active infections, or those on sleep medications may not benefit from this study.

Why it matters

Potential benefit: If successful, this study could significantly improve sleep quality and overall quality of life for women affected by breast cancer-related lymphedema.

How similar studies have performed: While similar studies have explored physiotherapy for lymphedema, this specific approach focusing on sleep quality and quality of life is relatively novel.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Participants must be aged between 18 or 85 years,
* with a diagnosis of unilateral lymphedema in the upper extremity following breast cancer surgery
* stage 2 lymphedema confirmed by a doctor
* voluntary consent to participate in the study.

Exclusion Criteria:

* refusal to participate in the study
* development of lymphedema due to primary causes, presence of bilateral upper extremity lymphedema
* active soft tissue infection in the lymphedematous arm
* mental or cognitive disorders
* inability to communicate or cooperate
* acute deep vein thrombosis, arterial insufficiency in the upper extremity, systemic diseases that could cause edema other than lymphedema (e.g., renal failure, liver failure, heart failure)
* use of sleep medications or antidepressants

Where this trial is running

Bolu and 1 other locations

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Breast Cancer Related LymphedemaBreast Cancer-Related LymphedemaPhysiotherapy and RehabilitationSleep QualityLocal Tissue FluidQuality of Life
Last reviewed 2026-06-10 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.