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e-CHAMP: Enhancing Care for Hospitalized Older Adults With Memory Problems

This study is ongoing, but not recruiting participants.
Study NCT00182832.   Last updated on August 4, 2008.   Information provided by National Institute on Aging (NIA)

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Descriptive Information Fields
Brief Title  e-CHAMP: Enhancing Care for Hospitalized Older Adults With Memory Problems
Official Title  Enhancing Care for Hospitalized Older Adults With Cognitive Impairment
Brief Summary

The purpose of this study is to evaluate the effectiveness of a cognitive screening program coupled with a computerized decision support system in improving the quality of care for hospitalized older adults with cognitive impairment.

Detailed Description

A growing body of evidence demonstrates that older patients with cognitive impairment (CI) who are hospitalized for the management of their medical illnesses are especially vulnerable to hospital acquired complications such as falls, injuries, pressure ulcers, restraints, and delirium. These complications contribute to mortality, poorer functional status, limited rehabilitation, prolonged length of stay, increased institutionalization, and higher health care costs. Evidence suggests that interdisciplinary geriatric inpatient services improve care for hospitalized older adults without CI; however, their effectiveness among older adults with CI is less clear. One reason may be the ever-quickening pace of care in the hospital setting. Thus, matching geriatric evaluation and recommendations to the true pace of hospital care may be one mechanism to improve the care of older adults with CI.

A recent report from the Institute of Medicine suggested that integrating information technology (IT) into health care is the best route to improve the overall safety and quality of the health care system. The hypothesis of this study is that missed, delayed, post-hoc, and incomplete implementation of the geriatric service-based recommendations are significant factors explaining the poor outcomes among hospitalized older adults with cognitive impairment (CI). Wishard Memorial Hospital's physicians are already using a Computerized Decision Support System (CDSS), developed by the Regenstrief Institute, to guide their medical services. For this study, the content of this CDSS will be modified to the special needs of older adults with CI. A major advantage of such a system is reducing the time to implementation of geriatric recommendations with a specific focus on preventing the initiation of potentially harmful medications and procedures during the critical first 48 hours of hospitalization.

A total of 400 patients with cognitive impairment who have been hospitalized in a medical ward will be recruited for this study. Patients will be randomized to receive either standard care or the proactive screening program for CI combined with the modified CDSS. The electronic medical record for all patients will be reviewed for prescriptions for potentially inappropriate medications, urinary catheters, or physical restraints during the first 24 hours and the entire hospital stay. Medical records will be used to determine the total number of hospital acquired complications that may be related to CI; these include falls, injuries such as pulling out IV lines or urinary catheters, pressure ulcers, and new-onset delirium episodes that developed during hospitalization. Also, the time elapsed between screening for CI and the physician ordering a geriatric consultation will be calculated using the electronic medical record.

Study Phase
Study Type  Interventional
Study Design  Prevention, Randomized, Double Blind (Subject, Caregiver, Investigator), Active Control, Parallel Assignment, Efficacy Study
Primary Outcome Measure  Use of potentially inappropriate medications, urinary catheter or physical restraints, and length of time in initiating a referral order, as recorded in the electronic medical record [ Time Frame: baseline and at discharge ] [ Designated as safety issue: No ]
Total number of hospital acquired complications recorded in the medical record that may be related to cognitive impairment (CI) [ Time Frame: baseline and at discharge ] [ Designated as safety issue: No ]
Secondary Outcome Measure  Length and cost of hospital stay from discharge records and billing system [ Time Frame: baseline, at discharge, 6 months post-discharge ] [ Designated as safety issue: No ]
Condition  Cognitive Impairment
Delirium
Intervention  Behavioral: e-CHAMP (Enhancing Care for Hospitalized Older Adults with Cognitive Impairment)
Behavioral: Standard Care
MEDLINE PMIDs 15123850,   8264068,   7966844,   14687382,   10855596,   9143435
Links
Recruitment Information Fields
Recruitment Status  Active, not recruiting
Enrollment  400
Start Date  June 2006
Completion Date December 2008
Eligibility Criteria 

Inclusion Criteria:

  • 65 years of age or older
  • Hospitalized in a medical ward
  • Able to speak English
  • Cognitive impairment based on screening at time of hospital admission

Exclusion Criteria:

  • Previously enrolled in the study during prior hospitalization (for multiple admissions; only data from the first admission will be used)
  • Enrolled in another clinical trial
  • Does not have cognitive impairment based on screening at time of hospital admission
Gender Both
Ages 65 Years and older
Accepts Healthy Volunteers No
Contacts ††
Location Countries  United States
Administrative Information Fields
NCT ID  NCT00182832
Organization ID IA0077
Secondary IDs †† K23AG026779-01
Study Sponsor  National Institute on Aging (NIA)
Collaborators ††
Investigators 
Principal Investigator:     Malaz Boustani, MD, MPH     Regenstrief Institute, IU Center for Aging Research    
Information Provided By National Institute on Aging (NIA)
Verification Date August 2008
First Received Date  September 9, 2005
Last Updated Date August 4, 2008

 †    Required WHO trial registration data element.
††   WHO trial registration data element that is required only if it exists.




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