About this trial
The aim of the study is to investigate the short-term (within 2 weeks) effects of resistance exercise with and without compression garments on lower limb lymphedema(LLL). Additionally, the study will explore the immediate response in LLL to resistance exercise (2 hours and 24 hours post-exercise).
Participants will continously wear a circumfencential sensor at the calf (CIMON from Icompression) under a compression garment and an activity tracker (SENS Motion from SENS Innovation Aps) at the thigh for 3 periods (two with supervised exercise sessions of 2 weeks and one control period).
Participants will attend supervised resistance exercise 2-3 times per week for 2 periods of 2 weeks (one with compression garment and one without). Assessments with the principal investigator will be scheduled before and after every 2 week period. Participants will keep a digital diary or diary in paper of their lymphedema related symptoms and experienced issues with the sensors or app.
Eligibility criteria
Qualifiers
verified diagnosis of lymphedema of the lower limb
completed compression bandaging
adherence to compression garment in daytime (minumum 5-6 days per week)
calf circumference > 35 and <75 cm
Disqualifiers
severe neuropathy of the lower leg
severe skin problems or wounds at the lower leg
cellulitis, DVT or acute injuries of the lower limb < 2 months prior to inclusion
ongoing adjuvant treatment for cancer
Trial design
Treatments tested in this trial
- Resistance exercise
Treatment groups
Locations
1Sponsors and collaborators
Carsten Bogh Juhl
Lead sponsor
Herlev and Gentofte Hospital
Sponsor institution