A Trial to Reduce Delirium in Aged Post Acute Patients

Aging Clinical Trial

Official title:

A Trial to Reduce Delirium in Aged Post Acute Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00182936
• Other study ID #: AG0040
• Secondary ID: AG17649
• Status: Completed
• Phase: Phase 3
• First received: September 13, 2005
• Last updated: November 16, 2006
• Start date: May 2000
• Est. completion date: June 2004

Study information

• Verified date: November 2006
• Source: National Institute on Aging (NIA)
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to develop a comprehensive Delirium Abatement Program of care of delirious patients in the post acute care setting and to evaluate its impact on persistence and severity of delirium and on functional recovery.

Description:

Common, morbid, and costly, delirium affects one third of hospitalized elders, and plays a central role in the cascade of adverse events that leads to functional decline and loss of independence. Moreover, as acute care stays continue to shorten and evidence mounts that delirium may persist for many weeks, concern about delirium can no longer be confined to the hospital. It is believed that a Delirium Abatement Program may significantly reduce the persistence of delirium in post-acute settings, and thereby improve functional recovery both during the post-acute stay and after discharge.

The Delirium Abatement Program (DAP) will be designed to assist facility staff to 1) detect delirium among new admissions, 2) evaluate common underlying causes of delirium, 3) prevent complications commonly associated with delirium, and 4) restore delirious patients' cognitive, behavioral, social and self care functioning to baseline status.

This three year trial will enroll 500 delirious patients admitted to eight Boston area post-acute skilled nursing facilities. The DAP intervention will be carried out in four facilities. Four other facilities, matched to the intervention by demographic, facility, and clinical characteristics, will serve as controls. Patients will be recruited within 72 hours (maximum 120 hrs) of admission, assessed weekly while in the facility, and at one, three, and six months following admission.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 500
• Est. completion date: June 2004
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 65 Years and older

Eligibility

Inclusion Criteria:

• Admission to study site following acute care medical/surgical hospitalization

• Aged 65 or older

• English-speaking

• Communicative prior to acute illness

• Not admitted for terminal care (life expectancy greater than 6 months)

• Residence within 25 miles of research site

Exclusion Criteria:

• Significant hearing impairment which precludes interviews

• End stage dementia (complete ADL dependence)

• Previous study enrollment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Aging
• Delirium

Intervention

Behavioral:
• Delirium Abatement Program

Locations

Country	Name	City	State
United States	Hebrew Rehabilitation Center for Aged	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
National Institute on Aging (NIA)	Paul B. Beeson Career Development Awards in Aging Research Program

Country where clinical trial is conducted

United States, 

References & Publications (7)

Bergmann MA, Murphy KM, Kiely DK, Jones RN, Marcantonio ER. A model for management of delirious postacute care patients. J Am Geriatr Soc. 2005 Oct;53(10):1817-25. — View Citation

Levkoff SE, Evans DA, Liptzin B, Cleary PD, Lipsitz LA, Wetle TT, Reilly CH, Pilgrim DM, Schor J, Rowe J. Delirium. The occurrence and persistence of symptoms among elderly hospitalized patients. Arch Intern Med. 1992 Feb;152(2):334-40. — View Citation

Lipowski ZJ. Delirium in the elderly patient. N Engl J Med. 1989 Mar 2;320(9):578-82. Review. — View Citation

Marcantonio ER, Flacker JM, Michaels M, Resnick NM. Delirium is independently associated with poor functional recovery after hip fracture. J Am Geriatr Soc. 2000 Jun;48(6):618-24. — View Citation

Marcantonio ER, Kiely DK, Simon SE, John Orav E, Jones RN, Murphy KM, Bergmann MA. Outcomes of older people admitted to postacute facilities with delirium. J Am Geriatr Soc. 2005 Jun;53(6):963-9. — View Citation

Marcantonio ER, Simon SE, Bergmann MA, Jones RN, Murphy KM, Morris JN. Delirium symptoms in post-acute care: prevalent, persistent, and associated with poor functional recovery. J Am Geriatr Soc. 2003 Jan;51(1):4-9. — View Citation

Simon SE, Bergmann MA, Jones RN, Murphy KM, Orav EJ, Marcantonio ER. Reliability of a structured assessment for nonclinicians to detect delirium among new admissions to postacute care. J Am Med Dir Assoc. 2006 Sep;7(7):412-5. Epub 2006 May 30. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Prevalence of delirium at two weeks after admission
Primary	Activities of Daily Living (ADL) functional improvement two weeks after admission
Primary	Full ADL functional recovery to pre-illness status three months after post-acute admission
Secondary	Examination of differences between patients in facilities receiving the Delirium Abatement Program and those not on additional outcomes of delirium persistence and ADL improvement one month following admission
Secondary	Differences in delirium severity, length of post acute stay, and health care resource utilization