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Pressure Ulcer Multi-disciplinary Teams Via Telemedicine (PUMTT): A Trial in Long Term Care (PUMTT)

Primary Purpose

Pressure Ulcers, Multi-disciplinary Wound Care Teams, Remote Support

Status
Completed
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Exposure to multi-disciplinary wound care team
Sponsored by
University of Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Pressure Ulcers

Eligibility Criteria

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

Inclusion Criteria:

  • LTC facility must be located within the Toronto Central or Central LHIN geographic boundaries.
  • LTC facility must be <100 km from the St. Michael's Hospital wound care team.
  • LTC facility must be entering data into MDS.
  • LTC facility administrator must consent to participate.
  • LTC facility must report a PU prevalence rate >5.5% in the 4th quarter 2009 MDS. [This is the average pressure ulcer prevalence rate for Ontario LTC facilities as reported by the Canadian Institute of Health Information (CIHI) in the 4th quarter 2009.]
  • Individual with PU (or Substitute Decision Maker (SDM)) must provide informed consent.

Exclusion Criteria:

  • LTC facility <100 beds.
  • LTC facility >100 km from the St. Michael's Hospital wound care team
  • LTC facility reporting a PU prevalence rate < 5.5% in the 4th quarter 2009 MDS.

Sites / Locations

  • 12 Long Term Care Facilities

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Multi-disciplinary wound care team

Arm Description

Stepped wedge study design i.e. start date of exposure is randomized.

Outcomes

Primary Outcome Measures

Rate of reduction in wound surface area (cm2/days)

Secondary Outcome Measures

Percentage of wounds healed

Full Information

First Posted
October 29, 2010
Last Updated
September 27, 2012
Sponsor
University of Toronto
Collaborators
Ontario Ministry of Health and Long Term Care, Canadian Patient Safety Institute, Central Community Care Access Center
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1. Study Identification

Unique Protocol Identification Number
NCT01232764
Brief Title
Pressure Ulcer Multi-disciplinary Teams Via Telemedicine (PUMTT): A Trial in Long Term Care
Acronym
PUMTT
Official Title
Pressure Ulcer Multi-disciplinary Teams Via Telemedicine (PUMTT): A Cluster Pragmatic Randomised Controlled Trial in Long Term Care
Study Type
Interventional

2. Study Status

Record Verification Date
September 2012
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Toronto
Collaborators
Ontario Ministry of Health and Long Term Care, Canadian Patient Safety Institute, Central Community Care Access Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the effectiveness of 'enhanced' multi-disciplinary wound care teams (MDTs) vs. 'usual' care teams in Long Term Care (LTC) facilities in Ontario for the treatment of pressure ulcers. LTC facilities with more than 100 beds that are within a 100 km distance from St. Mikes and have a problem with pressure ulcers will be asked to participate. A total of 10 LTC facilities will be randomly selected (i.e. selected by chance) from those that agree to participate. The 'enhanced' MDT will be an Advance Practice Nurse(APN) with expertise in wound care who has direct access to the wound care team at St. Mikes. This APN will develop treatment plans in consultation with facility staff, providing targeted pressure ulcer treatment education on an ongoing, case by case basis. Care is supported by telemedicine with the use of digital photography and online communication between members of the care team. This study is a stepped wedge randomized trial, meaning LTC facilities are assigned to a start date for this study totally by chance. Changes in healing rates, wound related pain, cost, number of new pressure ulcers, and number of wounds healed will be measured before, and after the APN is introduced to facilities. In order to gain more insight into how people felt about this model of care, interviews will be held with individuals and groups of staff at 5 randomly selected facilities before, during, and after the study has been completed.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pressure Ulcers, Multi-disciplinary Wound Care Teams, Remote Support, Digital Wound Photography

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Phase 3
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
137 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Multi-disciplinary wound care team
Arm Type
Experimental
Arm Description
Stepped wedge study design i.e. start date of exposure is randomized.
Intervention Type
Other
Intervention Name(s)
Exposure to multi-disciplinary wound care team
Intervention Description
Phase 1: In Person Support (3 mths) Advance Practice Nurses (APNs) affiliated with Enhanced Multi-Disciplinary visit LTC facilities on a weekly basis. The APN may communicate with other members of an EMDT via telephone or online.EMDTs will collectively teach and mentor LTC facility wound care teams throughout the study. Phase 2: Remote Support (2-11 mths) In the second phase, EMDTs will support LTC facility staff remotely via telephone and online communication, visiting the facilities on an as needed basis only. All PU treatment will be based on RNAO evidence-based guidelines (updated in 2007)contextualized to the LTC setting.
Primary Outcome Measure Information:
Title
Rate of reduction in wound surface area (cm2/days)
Time Frame
6 mths
Secondary Outcome Measure Information:
Title
Percentage of wounds healed
Time Frame
6 mths

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: LTC facility must be located within the Toronto Central or Central LHIN geographic boundaries. LTC facility must be <100 km from the St. Michael's Hospital wound care team. LTC facility must be entering data into MDS. LTC facility administrator must consent to participate. LTC facility must report a PU prevalence rate >5.5% in the 4th quarter 2009 MDS. [This is the average pressure ulcer prevalence rate for Ontario LTC facilities as reported by the Canadian Institute of Health Information (CIHI) in the 4th quarter 2009.] Individual with PU (or Substitute Decision Maker (SDM)) must provide informed consent. Exclusion Criteria: LTC facility <100 beds. LTC facility >100 km from the St. Michael's Hospital wound care team LTC facility reporting a PU prevalence rate < 5.5% in the 4th quarter 2009 MDS.
Facility Information:
Facility Name
12 Long Term Care Facilities
City
Toronto
State/Province
Ontario
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
24559218
Citation
Stern A, Mitsakakis N, Paulden M, Alibhai S, Wong J, Tomlinson G, Brooker AS, Krahn M, Zwarenstein M. Pressure ulcer multidisciplinary teams via telemedicine: a pragmatic cluster randomized stepped wedge trial in long term care. BMC Health Serv Res. 2014 Feb 24;14:83. doi: 10.1186/1472-6963-14-83.
Results Reference
derived
Links:
URL
http://www.theta.utoronto.ca
Description
Toronto Health Economic Technology Assessment collaborative

Learn more about this trial

Pressure Ulcer Multi-disciplinary Teams Via Telemedicine (PUMTT): A Trial in Long Term Care

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