Evaluation of Pressure Applying Efficiency in Multi-Layer Bandaging
1 other identifier
observational
37
1 country
1
Brief Summary
Lymphedema is a condition characterized by excess accumulation of protein rich tissue fluid in interstitial spaces. It is a progressive chronic disease and without appropriate management may result in serious complications. In Israel, patients are referred to physiotherapists certified in treatment for lymphedema. According to the International Society of Lymphology (ISL) the best treatment is a holistic, multidiscipline approach. Amongst the different methods of lymphedema management, the use of compression is the only treatment that has shown to be effective in randomized controlled trials. The ISL recommends that patients with lymphedema in the lower limb ought to bandage their leg with multi-layer bandaging on a daily basis for a period of two to four weeks. A new classification system for compression bandages was recommended; pressure of \<20 mmHg was categorized as mild, 20-40 mmHg as medium, 40-60 mmHg as strong and ≥60 mmHg as very strong. In patients with leg edema, bandages with strong pressure were shown to be the most effective. However, in the presence of a venous ulcer on a lymphatic leg, pressure between 35 and 45 mmHg is the widely accepted range for sufficient and safe compression. The use of measurement instruments is currently the only realistic method for determining the actual pressure achieved beneath the bandage. However, it is neither economical nor feasib¬le nor is it realistic in terms of time. Recent studies show that many healthcare professionals use inadequate sub-bandage pressure. No study so far has focused on therapists that are trained in lymphatic treatment. In spite of correct pressure bandaging importance, the question whether physiotherapists succeed in correctly applying it is left unanswered. The main purpose of this study is to evaluate the pressure applying efficiency in multi-layer bandaging among physiotherapists in Israel who treat lymphedema. 34 physiotherapists trained in lymphatic treatment will be recruited for this research. Each volunteer will receive a questionnaire concerning their self-perceived competence in the application of compression bandages. Afterwards, two practical trials will be held a week apart in which the subjects will be asked to apply bandages using strong and medium pressure. Using PicoPress®, pressure will be measured directly after bandaging and two hours later. Our hypothesis is that the majority of therapists will properly apply medium or strong pressure on the lower limbs.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Aug 2016
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 1, 2016
CompletedFirst Submitted
Initial submission to the registry
August 3, 2016
CompletedFirst Posted
Study publicly available on registry
August 5, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 23, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
April 23, 2017
CompletedAugust 16, 2017
June 1, 2016
9 months
August 3, 2016
August 13, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Sub-bandage pressure
Resting pressure will be measured directly after bandaging and two hours later using a PicoPress® measurement device.
Two hours
Eligibility Criteria
Physical Therapists who have been specifically trained in Lymphatic therapy and have administered these treatments in the past two years.
You may qualify if:
- Physical Therapists trained in Lymphatic treatments
You may not qualify if:
- Have not treated a Lymphatic patient in the past two years
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Assuta Hospital Systemslead
- Maccabi Healthcare Services, Israelcollaborator
- University of Haifacollaborator
Study Sites (1)
Maccabi Healthcare Services
Bat Yam, Israel
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Woldman Anat, BPT
Physical Therapist at Maccabi HMO
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 3, 2016
First Posted
August 5, 2016
Study Start
August 1, 2016
Primary Completion
April 23, 2017
Study Completion
April 23, 2017
Last Updated
August 16, 2017
Record last verified: 2016-06
Data Sharing
- IPD Sharing
- Will not share