Falls Prevention in Acute Care Hospital (PRECEPT)

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2010 by Centre Hospitalier Universitaire Vaudois.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by:
Centre Hospitalier Universitaire Vaudois
ClinicalTrials.gov Identifier:
NCT01054287
First received: January 21, 2010
Last updated: NA
Last verified: January 2010
History: No changes posted
  Purpose

The aim of this study is to evaluate the effect of a multifactorial falls prevention program in an acute internal medicine ward.


Condition Intervention
Falls
Other: Multifactorial falls prevention program
Other: No falls prevention intervention

Study Type: Interventional
Official Title: Falls Prevention Program in Acute Care Hospital

Further study details as provided by Centre Hospitalier Universitaire Vaudois:

Primary Outcome Measures:
  • falls rate [ Time Frame: 2 years ] [ Designated as safety issue: No ]

Arms Assigned Interventions
Experimental: Falls prevention Other: Multifactorial falls prevention program
Placebo Comparator: Usual care Other: No falls prevention intervention

  Eligibility

Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • all patients admitted to internal medicine ward

Exclusion Criteria:

  • none
  Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01054287

Contacts
Contact: Stephane Rochat, MD +41 21 314 5239 stephane.rochat@chuv.ch

Locations
Switzerland
Service of internal medicine, CHUV Not yet recruiting
Lausanne, Vaud, Switzerland, 1011
Contact: Stephane Rochat, MD    +41 21 3145239    stephane.rochat@chuv.ch   
Principal Investigator: Gerard Waeber, MD         
Sub-Investigator: Stephane Rochat, MD         
Sponsors and Collaborators
Centre Hospitalier Universitaire Vaudois
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT01054287     History of Changes
Other Study ID Numbers: SQO150
Study First Received: January 21, 2010
Last Updated: January 21, 2010
Health Authority: Switzerland: Federal Office of Public Health

ClinicalTrials.gov processed this record on September 11, 2014