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

This study has been completed.
Sponsor:
Collaborators:
Ontario Ministry of Health and Long Term Care
Canadian Patient Safety Institute
Central Community Care Access Center
Information provided by (Responsible Party):
Anita Stern, University of Toronto
ClinicalTrials.gov Identifier:
NCT01232764
First received: October 29, 2010
Last updated: September 27, 2012
Last verified: September 2012

October 29, 2010
September 27, 2012
October 2010
March 2012   (final data collection date for primary outcome measure)
Rate of reduction in wound surface area (cm2/days) [ Time Frame: 6 mths ]
Same as current
Complete list of historical versions of study NCT01232764 on ClinicalTrials.gov Archive Site
Percentage of wounds healed [ Time Frame: 6 mths ]
Same as current
Not Provided
Not Provided
 
Pressure Ulcer Multi-disciplinary Teams Via Telemedicine (PUMTT): A Trial in Long Term Care
Pressure Ulcer Multi-disciplinary Teams Via Telemedicine (PUMTT): A Cluster Pragmatic Randomised Controlled Trial in Long Term Care

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.

Not Provided
Interventional
Phase 3
Allocation: Randomized
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Health Services Research
  • Pressure Ulcers
  • Multi-disciplinary Wound Care Teams
  • Remote Support
  • Digital Wound Photography
Other: Exposure 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.

Experimental: Multi-disciplinary wound care team
Stepped wedge study design i.e. start date of exposure is randomized.
Intervention: Other: Exposure to multi-disciplinary wound care team
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
137
March 2012
March 2012   (final data collection date for primary outcome measure)

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.
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Canada
 
NCT01232764
25048
Yes
Anita Stern, University of Toronto
University of Toronto
  • Ontario Ministry of Health and Long Term Care
  • Canadian Patient Safety Institute
  • Central Community Care Access Center
Not Provided
University of Toronto
September 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP