Bioelectrical Impedance for Self-monitoring of Lymphedema
Primary Purpose
Lymphedema
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
self-monitor arm volume
Sponsored by
About this trial
This is an interventional supportive care trial for Lymphedema focused on measuring lymphedema, breast cancer, self care, bioelectrical impedance, monitoring
Eligibility Criteria
Inclusion Criteria:
- Healthy Volunteers for Phase 1: no known history of cancer or lymphatic disease.
- Lymphedema volunteers Phases 1 &2: history of breast cancer and diagnosis of lymphedema in one arm.
- All volunteers: ≥ 21 years of age.
Exclusion Criteria:
- Healthy Volunteers Phase 1: history of arm surgery or family history of primary lymphedema.
- Lymphedema volunteers Phases 1 & 2: bilateral lymphedema.
All volunteers:
- inability to stand upright;
- conditions that could cause swelling: pregnancy, congestive heart failure, liver failure;
- infection, open sores on arms, or known sensitivity to electrodes;
- pacemakers or internal defibrillators;
- currently undergoing IV chemotherapy or radiation; or
- use of laxatives or diuretics to lose weight.
Sites / Locations
- Vanderbilt Univeristy School Of Nursing
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
self-monitoring
completion of forms
Arm Description
participants will use bioelectrical impedance to self-monitor arm volume at home
participants will complete self-report forms
Outcomes
Primary Outcome Measures
self care behaviors
individual tasks initiated by a participant to care for their lymphedema that may vary from participant to participant.
Self-care self efficacy
perception of abilty to provide lymphedema self-care
Secondary Outcome Measures
health
lymphedema associated symptoms
quality of life
quality of life
economics
expense in terms of lost income or out-of pocket payments related to lymphedema.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01385488
Brief Title
Bioelectrical Impedance for Self-monitoring of Lymphedema
Official Title
Bioelectrical Impedance for Self-monitoring of Breast Cancer Related Lymphedema
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Breast cancer treatment-related lymphedema requires life-long self-care is required.
No objective measurement mechanism exists that can easily be used to self-monitor arm volume.
Bioelectrical impedance devices approved for lymphedema measurement may be able to be used for self-monitoring.
The investigators will conduct a two-part study to first develop an impedance driven self-measurement protocal and then test the protocol in home settings.
The investigators hypothesize in part two of the study that when compared to participants who are not self-monitoring, those who self-monitor limb volume will: 1) report more days of garment use, skin care, and simple-MLD; and, 2) have fewer, less distressful, less intense symptoms, better productivity/activity, report higher perceived self-management/self-efficacy and QOL; experience fewer missed days of work, lymphedema treatment days, arm infections, and have a smaller number of antibiotic prescriptions.
Detailed Description
Breast cancer treatment-related lymphedema (swelling) is an incurable, chronic condition experienced by a significant percentage of breast cancer survivors. It has many associated symptoms, negatively impacts quality of life (QOL), and increases health care costs. As with other chronic diseases, such as diabetes, life-long self-care is required. No objective measurement mechanism exists that can easily be used to self-monitor arm volume, a key self-care outcome. Those with lymphedema are forced to rely on visual recognition of increasing volume to know if their self-care is effective and when to seek treatment. Timely recognition of worsening swelling is believed to result in better patient outcomes; however, substantial volume increases often occur before observable changes are noted and this window of opportunity is missed. Many with lymphedema only seek care when they have developed infection in the swollen limb.
The inability to objectively monitor arm volume on a regular basis likely results in discomfort, poorer QOL, and increased health care costs.The broad, long-term objective of this application is to develop a method for monitoring arm lymphedema that can be used at home to improve lymphedema self-management and patient outcomes. To accomplish this, the investigators will conduct a two-phase, translational pilot study to explore the use of a hand-held bioelectrical impedance device as an arm volume self-measurement method.
The purpose of Phase 1 is to develop a bioelectrical impedance self-measurement protocol. Healthy volunteers (n=11) and individuals with lymphedema (n=11) will be in Phase 1 (protocol development). This will take place in laboratory and home settings. This Phase is not interventional and is not detailed in this posting.
The purpose of Phase 2 is to compare self-care activities and health and economic outcomes between breast cancer survivors with lymphedema following the self-monitoring protocol developed in Phase 1 and breast cancer survivors with lymphedema not on protocol (n=42).The protocol will be field-tested by breast cancer survivors with lymphedema in Phase 2 (a two group randomized clinical trial). One group will self-measure with impedance at home for three months, weekly record self-care activities, and will complete follow-up assessments. The other group will mirror Group 1 except for impedance measurements. This is an interventional study and is presented as such in this clinical trial posting.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphedema
Keywords
lymphedema, breast cancer, self care, bioelectrical impedance, monitoring
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
72 (Actual)
8. Arms, Groups, and Interventions
Arm Title
self-monitoring
Arm Type
Experimental
Arm Description
participants will use bioelectrical impedance to self-monitor arm volume at home
Arm Title
completion of forms
Arm Type
No Intervention
Arm Description
participants will complete self-report forms
Intervention Type
Behavioral
Intervention Name(s)
self-monitor arm volume
Intervention Description
bioelectrical impedance
Primary Outcome Measure Information:
Title
self care behaviors
Description
individual tasks initiated by a participant to care for their lymphedema that may vary from participant to participant.
Time Frame
4 months
Title
Self-care self efficacy
Description
perception of abilty to provide lymphedema self-care
Time Frame
4 months
Secondary Outcome Measure Information:
Title
health
Description
lymphedema associated symptoms
Time Frame
four months
Title
quality of life
Description
quality of life
Time Frame
4 months
Title
economics
Description
expense in terms of lost income or out-of pocket payments related to lymphedema.
Time Frame
4 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Healthy Volunteers for Phase 1: no known history of cancer or lymphatic disease.
Lymphedema volunteers Phases 1 &2: history of breast cancer and diagnosis of lymphedema in one arm.
All volunteers: ≥ 21 years of age.
Exclusion Criteria:
Healthy Volunteers Phase 1: history of arm surgery or family history of primary lymphedema.
Lymphedema volunteers Phases 1 & 2: bilateral lymphedema.
All volunteers:
inability to stand upright;
conditions that could cause swelling: pregnancy, congestive heart failure, liver failure;
infection, open sores on arms, or known sensitivity to electrodes;
pacemakers or internal defibrillators;
currently undergoing IV chemotherapy or radiation; or
use of laxatives or diuretics to lose weight.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sheila H Ridner, PHD
Organizational Affiliation
Vanderbilt University School of Nursing
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt Univeristy School Of Nursing
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37240
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Bioelectrical Impedance for Self-monitoring of Lymphedema
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