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Treatment Routes for Exploring Agitation (TREA)

Primary Purpose

Dementia, Behavior Problems

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
TREA (Treatment Routes for Exploring Agitation)
Placebo Control Group
Sponsored by
National Institute on Aging (NIA)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dementia focused on measuring Cognition disorder, nursing home residents, agitation, behavior disorder

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 60 or older
  • Diagnosis of dementia derived from the resident's medical chart at the facility or from an attending physician, as based on DSM-IV criteria and the Report of the NINCDS-ADRDA
  • Resident of the facility for at least three weeks so that nursing staff members know the resident well enough to accurately assess him or her
  • Identified by nursing staff to exhibit either verbal agitation or physical non-aggressive agitation at least several times a day

Exclusion Criteria:

  • Lifelong diagnosis of schizophrenia
  • Bipolar disorder diagnosed prior to onset of dementia
  • Diagnosis of premorbid mental retardation
  • Judged by direct-care nursing staff to have a life expectancy of less than 3 months
  • Expected to leave the nursing home (either to enter the hospital or to go home) within the next 4 months
  • Agitation manifested less than 6 times a day

Sites / Locations

  • Research Institute on AgingRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Outcomes

Primary Outcome Measures

Agitation Behavior Mapping Instrument (ABMI)

Secondary Outcome Measures

affect/mood measured by Lawton's behavior stream assessment

Full Information

First Posted
January 8, 2009
Last Updated
July 1, 2009
Sponsor
National Institute on Aging (NIA)
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1. Study Identification

Unique Protocol Identification Number
NCT00820859
Brief Title
Treatment Routes for Exploring Agitation
Acronym
TREA
Official Title
Treatment of Agitation in the Nursing Home
Study Type
Interventional

2. Study Status

Record Verification Date
July 2009
Overall Recruitment Status
Unknown status
Study Start Date
June 2006 (undefined)
Primary Completion Date
June 2011 (Anticipated)
Study Completion Date
June 2011 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
National Institute on Aging (NIA)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to examine the efficacy of non-pharmacological ways to treat agitated behaviors in nursing home residents with dementia. The hypothesis is that non-pharmacological interventions will be more effective than placebo in decreasing such behaviors.
Detailed Description
Clinicians often refer to elderly persons under their care as "agitated." However, agitation is not a diagnosis, but rather, a descriptive term pertaining to a group of behavioral signs and symptoms, defined as socially inappropriate verbal, vocal, or motor (physical) activity that is not judged by an outside observer to result directly from the needs or confusion of the agitated individual. While the literature reports positive effects of non-pharmacological interventions, most studies tend to be based on small samples and do not yield statistically significant results. This study examines the impact of non-pharmacologic interventions tailored through an algorithm labeled TREA (Treatment Routes for Exploring Agitation) using a large, well-controlled, systematic research design. TREA is an objective, systematic method for developing individualized non-pharmacological treatment plans based on an analysis of the agitated person's unmet needs, past and current preferences, past role-identity, cognitive, mobility, and sensory abilities/limitations, and possible causes for particular agitated behaviors. The methodology calls for ascertaining the type of agitated behavior and the most likely etiology, and then matching the intervention to the etiology and to the participant's characteristics. The protocol involves the following steps: Baseline assessment - using standardized assessments (e.g., MMSE, ABMI, CMAI, Self-identity in dementia), collecting background demographic and medical information as well as systematic observations of the agitated resident Intervention exploration - after analyzing potential unmet needs as well as preferences, abilities and identities of each participant, investigators develop a list of potentially successful interventions, examining the effectiveness of a wide range of interventions, from family videos to manipulatives (e.g., puzzles, a tool kit) Intervention (treatment) phase - Interventions are systematically provided during the hours of highest agitation (determined at baseline) and observations are conducted at the same time. The treatment phase lasts for 10 days. The placebo control group includes a presentation to staff members as to how to intervene with behavior problems and similar observations of residents. Follow-up phase includes repeated assessments without interventions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia, Behavior Problems
Keywords
Cognition disorder, nursing home residents, agitation, behavior disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Active Comparator
Intervention Type
Behavioral
Intervention Name(s)
TREA (Treatment Routes for Exploring Agitation)
Intervention Description
Individualized non-pharmacological treatment plan for agitation
Intervention Type
Behavioral
Intervention Name(s)
Placebo Control Group
Intervention Description
A presentation on the treatment of behavior problems in dementia given to the staff caregivers of the comparison group
Primary Outcome Measure Information:
Title
Agitation Behavior Mapping Instrument (ABMI)
Time Frame
10 days of intervention vs. 10 days of baseline
Secondary Outcome Measure Information:
Title
affect/mood measured by Lawton's behavior stream assessment
Time Frame
10 days of intervention vs. 10 days of baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 60 or older Diagnosis of dementia derived from the resident's medical chart at the facility or from an attending physician, as based on DSM-IV criteria and the Report of the NINCDS-ADRDA Resident of the facility for at least three weeks so that nursing staff members know the resident well enough to accurately assess him or her Identified by nursing staff to exhibit either verbal agitation or physical non-aggressive agitation at least several times a day Exclusion Criteria: Lifelong diagnosis of schizophrenia Bipolar disorder diagnosed prior to onset of dementia Diagnosis of premorbid mental retardation Judged by direct-care nursing staff to have a life expectancy of less than 3 months Expected to leave the nursing home (either to enter the hospital or to go home) within the next 4 months Agitation manifested less than 6 times a day
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jiska Cohen-Mansfield, PhD
Phone
301-770-8453
Email
cohen-mansfield@hebrew-home.org
First Name & Middle Initial & Last Name or Official Title & Degree
Marcia S. Marx, PhD
Phone
301-770-8451
Email
marx@hebrew-home.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jiska Cohen-Mansfield, PhD
Organizational Affiliation
Research Institute on Aging
Official's Role
Principal Investigator
Facility Information:
Facility Name
Research Institute on Aging
City
Rockville
State/Province
Maryland
ZIP/Postal Code
20814
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jiska Cohen-Mansfield, PhD, ABPP
Phone
301-770-8453
Email
cohen-mansfield@hebrew-home.org
First Name & Middle Initial & Last Name & Degree
Marcia Marx, PhD
Phone
301-770-8451
Email
marx@hebrew-home.org
First Name & Middle Initial & Last Name & Degree
Jiska Cohen-Mansfield, PhD, ABPP
First Name & Middle Initial & Last Name & Degree
Marcia Marx, PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
18394647
Citation
Cohen-Mansfield J. Agitated behavior in persons with dementia: the relationship between type of behavior, its frequency, and its disruptiveness. J Psychiatr Res. 2008 Nov;43(1):64-9. doi: 10.1016/j.jpsychires.2008.02.003. Epub 2008 Apr 3.
Results Reference
background
PubMed Identifier
17702884
Citation
Cohen-Mansfield J, Libin A, Marx MS. Nonpharmacological treatment of agitation: a controlled trial of systematic individualized intervention. J Gerontol A Biol Sci Med Sci. 2007 Aug;62(8):908-16. doi: 10.1093/gerona/62.8.908.
Results Reference
background
PubMed Identifier
2715584
Citation
Cohen-Mansfield J, Marx MS, Rosenthal AS. A description of agitation in a nursing home. J Gerontol. 1989 May;44(3):M77-84. doi: 10.1093/geronj/44.3.m77.
Results Reference
background
PubMed Identifier
23059151
Citation
Cohen-Mansfield J, Thein K, Marx MS, Dakheel-Ali M, Freedman L. Efficacy of nonpharmacologic interventions for agitation in advanced dementia: a randomized, placebo-controlled trial. J Clin Psychiatry. 2012 Sep;73(9):1255-61. doi: 10.4088/JCP.12m07918.
Results Reference
derived
Links:
URL
http://www.researchinstituteonaging.org/
Description
Research Institute on Aging

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Treatment Routes for Exploring Agitation

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