Clinical Trials Logo

Clinical Trial Summary

Background: The incidence of lower limb lymphedema (LLL) after gynecological cancer surgery with lymphadenectomy is about 10-46%. Lower limb lymphedema results in limited physical mobility and reduced patients' quality of life. A hospital -based complete decongestive therapy has been recommended to patients with LLL, including exercise, manual lymphatic drainage, compression therapy, and skin care. However, the inconvenience of the hospital-based rehabilitation program limit the availability for those patients LLL. Home-based exercise program may be feasible instead of the hospital-based program. Few studies have evaluated the effectiveness of the home-based lower extremity exercise on reliving LLL and improving quality of life in patients with LLL. Research Purposes: The main purpose of the study is to evaluate the effectiveness of a home-based exercise program for relieving lower extremity lymphedema, including circumference measurement, bioimpedance spectroscopy (BIS), lower limb muscle strength, quality of life related to cancer & LLL, and fatigue. Methods: This study is a two- year project with a single-blind randomized clinical trial. The participants are women with gynecological cancer surgery, aged of 20-75 years and currently have lower extremity lymphedema. A sample of 76 participants will be stratified randomly assigned to an experimental group or a control group. The experimental group is to carry out a home-based anti-resistance exercise with elastic band other than a routine care of complex decongestive physiotherapy; while the control group is to carry out a routine care of complex decongestive physiotherapy. The home-based program is a 12-week exercise program. Data collections will be conducted before exercise (Baseline), during exercise (second months), and exercise program after completion. Measures includes (1) Physical examination: limb leg circumference measurement, bioimpedance spectroscopy (BIS), lower limb muscle strength, (2) Questionnaires: Functional status of lymphatic edema of LLL, fatigue, and EORTC-QLQ-C30. Anticipated Outcomes: Findings from this study could provide a reference of home-based exercise guideline and be integrated into the care of activities for women following gynecological surgery with LLL.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05003973
Study type Interventional
Source National Cheng Kung University
Contact Yu-Yun Hsu
Phone +886-6-2353535
Email yuht12@mail.ncku.edu.tw
Status Not yet recruiting
Phase N/A
Start date August 20, 2021
Completion date December 31, 2023

See also
  Status Clinical Trial Phase
Completed NCT03935698 - Physiotherapy Treatment in Women With Dyspareunia Following Gynecological Cancer: a Pilot Study N/A
Completed NCT01831089 - Phase I Study of Lurbinectedin (PM01183) in Combination With Paclitaxel, With or Without Bevacizumab, in Selected Advanced Solid Tumors Phase 1
Completed NCT01703585 - Feasibility Study of Genomic Profiling Methods and Timing in Tumor Samples
Completed NCT04694508 - Intraoperative Music Therapy in Gynecological Oncology N/A
Recruiting NCT03714581 - Laser Therapy Following Radiotherapy for Gynecological Cancer N/A
Recruiting NCT03740503 - Genomic Investigation of Unusual Responders
Completed NCT02169908 - Analysis of Chronic Neuropathic Pain Markers in Patients Treated With Oxaliplatin N/A
Recruiting NCT05028504 - A Phase II Study of Anlotinib Combined With Penpulimab in Subjects With Gynecological Cancer Phase 2
Completed NCT02026687 - Recovery and Analgesia After Surgery for Gynecological Cancer Phase 4
Active, not recruiting NCT04341480 - The Safety of Chemotherapy for Patients With Gynecological Malignancy in High-risk Region of COVID-19
Recruiting NCT04236362 - A Study of TQB2450 Combined With Anlotinib in Subjects With Gynecological Cancer Phase 1/Phase 2
Not yet recruiting NCT06039306 - Perioperative Immunonutrition Under Enhanced Recovery After Surgery N/A
Recruiting NCT02906943 - Ontario-wide Cancer TArgeted Nucleic Acid Evaluation
Completed NCT03553784 - Low-Intensity CBT for Gynaecological Cancer Survivors N/A