Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Interdisciplinary Mobility Approach To Reduction Of Facility-Acquired Pressure Ulcers (TEAM)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01008254
Recruitment Status : Completed
First Posted : November 5, 2009
Last Update Posted : October 19, 2011
Sponsor:
Collaborator:
Robert Wood Johnson Foundation
Information provided by (Responsible Party):
Tracey L. Yap, University of Cincinnati

Study Description
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
Musical reminder will raise compliance with mobility in the long-term care setting and reduce facility-acquired pressure ulcers.

Condition or disease Intervention/treatment Phase
Pressure Ulcers Behavioral: Musical prompt Behavioral: Delayed musical prompt Other: No musical prompt Phase 2 Phase 3

Study Design
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 2000 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Interdisciplinary Mobility Approach To Reduction Of Facility-Acquired Pressure Ulcers
Study Start Date : September 2009
Actual Primary Completion Date : May 2011
Actual Study Completion Date : May 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Pressure Sores

Arms and Interventions
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Arm Intervention/treatment
Experimental: Musical prompt Behavioral: Musical prompt
Repositioning and mobility education program administered to all facility staff combined with tailored musical prompt reminder that played every two hours, every day, during a 12 hour period, for 12 months.
Active Comparator: Delayed musical prompt Behavioral: Delayed musical prompt
Repositioning and mobility education program administered to all facility staff combined with tailored musical prompt reminder that played every two hours, every day, during a 12 hour period, for 6 months.
No Intervention: No musical prompt Other: No musical prompt
No intervention.


Outcome Measures
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. Reduction of Facility Acquired Pressure Ulcers [ Time Frame: 2 years ]

Secondary Outcome Measures :
  1. Organizational Change [ Time Frame: 2 years ]

Eligibility Criteria
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Long-term care resident
  • MDS qualified

Exclusion Criteria:

  • Self pay long-term care residents
Contacts and Locations
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01008254


Sponsors and Collaborators
University of Cincinnati
Robert Wood Johnson Foundation
Investigators
Layout table for investigator information
Principal Investigator: Tracey L Yap, RN, PhD University of Cincinnati College of Nursing
More Information
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Layout table for additonal information
Responsible Party: Tracey L. Yap, Assistant Professor, University of Cincinnati
ClinicalTrials.gov Identifier: NCT01008254     History of Changes
Other Study ID Numbers: #1007523
First Posted: November 5, 2009    Key Record Dates
Last Update Posted: October 19, 2011
Last Verified: October 2011
Additional relevant MeSH terms:
Layout table for MeSH terms
Pressure Ulcer
Ulcer
Pathologic Processes
Skin Ulcer
Skin Diseases