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Community RCT of the Effectiveness of Two Compression Bandaging Technologies

Primary Purpose

Venous Ulcer

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Four-layer Bandage (Elastomeric)
Short-stretch Bandage (Non-elastomeric)
Sponsored by
Queen's University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Venous Ulcer focused on measuring leg ulcer, compression, bandage, APBI, venous insufficiency

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: clinical presentation of venous insufficiency leg ulcer equal to or larger than 0.7 cm in any one dimension ulcer a minimum duration of 1 week ankle brachial pressure index equal to or greater than 0.80 participant can provide written consent participant can communicate in English, or translation available participant 18 years or over Exclusion Criteria: diagnosed with Diabetes Mellitus - insulin dependent or participant on oral hypoglycemics participants who failed to improve over a 3-month period after being treated with either the SS or 4-layer compression bandaging system prior to the trial previous trial patients (ie individuals previously enrolled in the study but now have recurrence or a new ulcer) symptoms of cognitive impairment noted

Sites / Locations

  • Winnipeg Regional Health Authority
  • Nursing Practice Solutions
  • VON Hamilton Branch
  • Saint Elizabeth Health Care
  • Kingston Chronic Wound Clinic
  • ParaMed Health Services
  • ET Now
  • Carefor
  • ParaMed Health Services
  • St. Joseph's Care Group
  • St. Michael's Hospital
  • ParaMed Home Health Care
  • Comcare Health
  • Ostomy and Wound Care Centre
  • Saskatoon Health Region Home Care

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

1

2

Arm Description

Clients randomized to short-stretch bandaging application

Clients randomized to four-layer bandaging application

Outcomes

Primary Outcome Measures

4 weeks or greater improvement in time-to-healing with short-stretch bandages compared to the four-layer bandaging system

Secondary Outcome Measures

rate of reduction in ulcer area
quality of life
expenditures over a one-year follow-up
Recurrence

Full Information

First Posted
September 16, 2005
Last Updated
November 18, 2015
Sponsor
Queen's University
Collaborators
Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT00202267
Brief Title
Community RCT of the Effectiveness of Two Compression Bandaging Technologies
Official Title
Community Randomised Control Trial of the Effectiveness of Two Compression Bandaging Technologies
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
January 2004 (undefined)
Primary Completion Date
March 2008 (Actual)
Study Completion Date
December 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen's University
Collaborators
Canadian Institutes of Health Research (CIHR)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Leg ulcers are emotionally distressing and painful, and often require months or years to heal. Although rarely acknowledged as a pressing health care issue, leg ulcers comprise a common, complex, and costly condition, managed primarily through community home care services. Indeed, leg ulcers are the most frequently seen and treated chronic wound. There is consensus in recent international, evidence-based practice guidelines that graduated, multi-layer compression is the most effective treatment, and greatly reduces healing time. High compression is more effective than low compression. However, there is no clear evidence as to which high compression technology is the most effective in promoting healing, the most acceptable to patients, or the most cost-effective to the health care system. This study is designed to answer these questions through a randomized trial conducted in the community, where most leg ulcer care currently takes place. Issues such as effectiveness in healing, quality of life, physical discomfort, personal preference, cost to the system and to the individual will be taken into consideration in evaluating two most commonly used types of compression bandaging.
Detailed Description
Background: Although rarely recognized as a pressing health care problem, leg ulcers comprise a common, complex, and costly condition. Over 80% of ongoing management of chronic wounds occurs in the community, and leg ulcers are one of the most frequently seen chronic wounds. The cost of leg ulcer care is considerable, being reported in both the UK and France to account for 2% of their total national health budgets. In Canada, the impact is only now being recognized due to the pressure on home care caseloads resulting from hospital downsizing, nursing shortages, and growing numbers of complex health populations. In one Ontario study, the care for fewer than 200 community leg ulcer cases cost in excess of $1.5 million for supplies and nursing visits, which translates to $100s of millions yearly Canada-wide. The impact on the individual is significant--chronic, painful, and often takes years to heal. Two-thirds of individuals with leg ulcers have at least one recurrence, and 45% have a history with the condition dating back 10 years. State of Knowledge & Clinical Practice Guidelines: Over the past decade, evidence from RCT studies and a recent Cochrane systematic review in BMJ demonstrated that venous leg ulcers treated with compression therapy are more likely to heal. Multi-layer high compression systems are more effective than low compression. However, the small number of people in trials comparing different high compression systems meant the review was unable to draw conclusions about their relative merit. Four of these trials have compared 4-layer bandage with short stretch technologies--the most commonly used technologies in Canada. In total, these trials involved only 220 patients, and were thus underpowered. Furthermore, they did not consider factors such as client preference and ease of use, or incorporate an economic evaluation. Plan of Investigation: The study will be a multi-centre, pragmatic, randomised trial of two types of compression bandaging technologies, incorporating an economic evaluation. Research objective: To compare the effectiveness of 2 high compression technologies delivered in the community on ulcer healing, recurrence rates, quality of life, and cost-effectiveness. Interventions: Four-layer bandage vs. Short-stretch bandage. Sample size: 414 total, 207 in each arm (80% power, " 0.05 to detect 4 week difference in time to heal). Inclusion Criteria: leg ulcer>1 cm in any one dimension, minimum duration of 1 week, ABPI>0.7. Randomization: will be carried out and stratified by: Clinical Centre (3 Health Regions in Ontario); Margolis' Prognostic Model (ulcer area and duration), Ulcer episode (1st or recurrent ulcer). Analysis: Primary outcome: time-to-healing of the reference ulcer. Secondary outcomes: quality of life & expenditures for treatment. Durability of healing will be assessed-follow-up for up to 52 weeks post-healing to determine recurrence rates associated with both technologies. Summary: There is consensus internationally in recommending the application of graduated multi-layer compression. High compression is more effective than low compression; however, there is no clear evidence as to which high compression technology is more effective.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Venous Ulcer
Keywords
leg ulcer, compression, bandage, APBI, venous insufficiency

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
426 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Clients randomized to short-stretch bandaging application
Arm Title
2
Arm Type
Active Comparator
Arm Description
Clients randomized to four-layer bandaging application
Intervention Type
Device
Intervention Name(s)
Four-layer Bandage (Elastomeric)
Other Intervention Name(s)
Profore bandaging system (Smith & Nephew Medical Ltd.)
Intervention Description
Precise components of the four-layer system depend on the circumference of the ankle. All the bandages are discarded after a single use, usually one week.
Intervention Type
Device
Intervention Name(s)
Short-stretch Bandage (Non-elastomeric)
Other Intervention Name(s)
Comprilan (Beiersdorf-Jobst, Inc.)
Intervention Description
These bandages are applied in a figure-eight technique; two bandages are applied at full extension in opposite directions up the leg (i.e., clockwise and counter clockwise). The participant will wash the short-stretch wherever possible and reused. The number of bandages supplied to each patient will be recorded on the visit record.
Primary Outcome Measure Information:
Title
4 weeks or greater improvement in time-to-healing with short-stretch bandages compared to the four-layer bandaging system
Time Frame
Time to healing or up to 12 months; post-healing follow-up
Secondary Outcome Measure Information:
Title
rate of reduction in ulcer area
Time Frame
Baseline and time of healing
Title
quality of life
Time Frame
Baseline and every 3 months
Title
expenditures over a one-year follow-up
Time Frame
From baseline to time of healing
Title
Recurrence
Time Frame
Status recorded at last visit of each month; one year post-healing follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: clinical presentation of venous insufficiency leg ulcer equal to or larger than 0.7 cm in any one dimension ulcer a minimum duration of 1 week ankle brachial pressure index equal to or greater than 0.80 participant can provide written consent participant can communicate in English, or translation available participant 18 years or over Exclusion Criteria: diagnosed with Diabetes Mellitus - insulin dependent or participant on oral hypoglycemics participants who failed to improve over a 3-month period after being treated with either the SS or 4-layer compression bandaging system prior to the trial previous trial patients (ie individuals previously enrolled in the study but now have recurrence or a new ulcer) symptoms of cognitive impairment noted
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Margaret B Harrison, PhD
Organizational Affiliation
Queen's University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ian D Graham, PhD
Organizational Affiliation
University of Ottawa (co-investigator)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Elizabeth A Nelson, PhD
Organizational Affiliation
University of Leeds, UK (co-investigator)
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Karen Lorimer, MNSc
Organizational Affiliation
Victorian Order of Nurses (co-investigator)
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Connie Harris, MNSc
Organizational Affiliation
ET NOW (co-investigator)
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Elizabeth VanDenKerkhof, PhD
Organizational Affiliation
School of Nursing, Queen's University
Official's Role
Study Director
Facility Information:
Facility Name
Winnipeg Regional Health Authority
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3G 0N6
Country
Canada
Facility Name
Nursing Practice Solutions
City
Fort Erie
State/Province
Ontario
ZIP/Postal Code
L2A 2G4
Country
Canada
Facility Name
VON Hamilton Branch
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 5G8
Country
Canada
Facility Name
Saint Elizabeth Health Care
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 1G8
Country
Canada
Facility Name
Kingston Chronic Wound Clinic
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7L 5E4
Country
Canada
Facility Name
ParaMed Health Services
City
Kingston
State/Province
Ontario
ZIP/Postal Code
K7M 8R1
Country
Canada
Facility Name
ET Now
City
Kitchener
State/Province
Ontario
ZIP/Postal Code
N2H 3K5
Country
Canada
Facility Name
Carefor
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1K 3B8
Country
Canada
Facility Name
ParaMed Health Services
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1Z 6X3
Country
Canada
Facility Name
St. Joseph's Care Group
City
Thunder Bay
State/Province
Ontario
ZIP/Postal Code
P7B 5G7
Country
Canada
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B 1W8
Country
Canada
Facility Name
ParaMed Home Health Care
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1V2
Country
Canada
Facility Name
Comcare Health
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5S 2T9
Country
Canada
Facility Name
Ostomy and Wound Care Centre
City
Regina
State/Province
Saskatchewan
ZIP/Postal Code
S4S 0S4
Country
Canada
Facility Name
Saskatoon Health Region Home Care
City
Saskatoon
State/Province
Saskatchewan
ZIP/Postal Code
S7H 4W3
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
23388350
Citation
Vandenkerkhof EG, Hopman WM, Carley ME, Kuhnke JL, Harrison MB. Leg ulcer nursing care in the community: a prospective cohort study of the symptom of pain. BMC Nurs. 2013 Feb 6;12:3. doi: 10.1186/1472-6955-12-3.
Results Reference
derived
PubMed Identifier
23031428
Citation
Pham B, Harrison MB, Chen MH, Carley ME; Canadian Bandaging Trial Group. Cost-effectiveness of compression technologies for evidence-informed leg ulcer care: results from the Canadian Bandaging Trial. BMC Health Serv Res. 2012 Oct 2;12:346. doi: 10.1186/1472-6963-12-346.
Results Reference
derived
PubMed Identifier
21995267
Citation
Harrison MB, Vandenkerkhof EG, Hopman WM, Graham ID, Carley ME, Nelson EA; Canadian Bandaging Trial Group. The Canadian Bandaging Trial: Evidence-informed leg ulcer care and the effectiveness of two compression technologies. BMC Nurs. 2011 Oct 13;10:20. doi: 10.1186/1472-6955-10-20.
Results Reference
derived
Links:
URL
http://www.cihr-irsc.gc.ca/
Description
Canadian Institutes of Health Research

Learn more about this trial

Community RCT of the Effectiveness of Two Compression Bandaging Technologies

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