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CompletedNCT01232764PUMTTUpdated Sep 28, 2012

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

A Phase 3 interventional study of Exposure to multi-disciplinary wound care team in Pressure Ulcers, Multi-disciplinary Wound Care Teams and Remote Support, sponsored by University of Toronto. Completed at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-09-28.

Sponsored by University of Toronto · Phase 3, Interventional, and Health services research

Phase
Phase 3
Study type
Interventional
Enrollment
137
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Pressure Ulcers
  • Multi-disciplinary Wound Care Teams
  • Remote Support
  • Digital Wound Photography
03

In context

Pressure Ulcer

518 studies on the registry are indexed under Pressure Ulcer; 116 are open to participants now.

This study's enrollment of 137 is above the median of 70 across 394 interventional studies indexed under Pressure Ulcer.

Browse Pressure Ulcer studies →

Lead sponsor

University of Toronto is the lead sponsor of 397 studies on the registry; 59 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Phase 3
Primary purpose
Health services research
Allocation
Randomized
Masking
Single (Outcomes assessor)
Enrollment
137 participants (actual)

Study arms

  • Experimental
    Multi-disciplinary wound care team

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

    Other: Exposure to multi-disciplinary wound care team

Interventions

  • OtherExposure to multi-disciplinary wound care team

    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.

06

What researchers measure

Primary outcomes

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

    Time frame: 6 mths

Secondary outcomes

  1. Percentage of wounds healed

    Time frame: 6 mths

07

Study locations

1 site
  • 12 Long Term Care Facilities
    Toronto, Ontario, Canada
08

References and documents

Publications

  • 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. PubMed 24559218 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 28, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01232764
Lead sponsor
University of Toronto
Collaborators
Ontario Ministry of Health and Long Term Care, Canadian Patient Safety Institute, Central Community Care Access Center
Responsible party
Anita Stern (Researcher, University of Toronto) — Principal investigator
First posted
Nov 2, 2010
Start date
Oct 2010
Primary completion
Mar 2012
Completion
Mar 2012
Last update
Sep 28, 2012

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Sep 2012. You cannot join it, but the record below documents what was studied.

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