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Alzheimer's Disease Multiple Intervention Trial (ADMIT)

Primary Purpose

Alzheimer's Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Home based occupational therapy
Best practices primary care
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer's Disease

Eligibility Criteria

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

Patient Inclusion Criteria:

  • Currently a patient within Wishard Health Services in Central Indiana
  • Diagnosed with possible or probable Alzheimer's Disease
  • Age 45 or older
  • English speaking
  • Hear well enough to answer questions in person or by telephone
  • Community-dwelling (includes senior communities, but not skilled nursing facilities)
  • Caregiver willing to participate in the study
  • Willing to receive home visits
  • Lives in Indianapolis metro area and planning to continue care at primary care clinic

Caregiver Inclusion Criteria

  • Age 18 or older
  • English speaking
  • Hear well enough to answer questions in person or by telephone
  • Community-dwelling
  • Willing to receive home visits

Exclusion Criteria:

  • Not a current patient within Wishard Health Services
  • Does not speak English
  • Currently enrolled in another study
  • Non-community dwelling, or residing in a skilled nursing facility

Sites / Locations

  • Wishard Health Services

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Best practices primary care

Home based occupational therapy

Arm Description

Best practices primary care encompasses the collaborative care intervention tested in a prior clinical trial (Callahan CM et al. JAMA 2006).

The intervention group receives all of the components of best practice primary care in addition to a home-based intervention designed to slow functional decline.

Outcomes

Primary Outcome Measures

Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCS - ADLI)

Secondary Outcome Measures

Short Physical Performance Battery (SPPB)
Includes Side by Side Stand, Semi-Tandem Stand, Tandem Stand, Repeated Chair Stands, and 3 or 4 meter walk
Tandem Stand, eyes closed
One Leg Stand, eyes open
Mini Mental State Examination
Word List Learning
Delayed Word List Recall
Grip Strength
Neuropsychiatric Inventory (NPI)
Alzheimer's Disease Cooperative Studies Resource Use Scale
PHQ - 9
Depression
GAD - 7
Anxiety
Comorbid Conditions
Adverse Events

Full Information

First Posted
March 10, 2011
Last Updated
March 7, 2016
Sponsor
Indiana University
Collaborators
National Institute on Aging (NIA), Regenstrief Institute, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT01314950
Brief Title
Alzheimer's Disease Multiple Intervention Trial
Acronym
ADMIT
Official Title
Alzheimer's Disease Multiple Intervention Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
July 2010 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Indiana University
Collaborators
National Institute on Aging (NIA), Regenstrief Institute, Inc.

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to conduct a two-year randomized, controlled clinical trial to improve functioning among older adults with Alzheimer's disease by comparing a control group receiving best practices primary care with an intervention group receiving best practice primary care plus a home-based occupational therapy intervention.
Detailed Description
The proposed study builds on our findings from a previous clinical trial that demonstrated the effectiveness of collaborative care for older adults with Alzheimer's disease cared for in primary care practices. In the prior trial, we demonstrated that guideline-level medical care resulted in improved quality of care and improved behavioral and psychological symptoms over one year among patients and their caregivers. However, despite finding significant differences among study groups on Neuropsychiatric Inventory scores, we did not find a significant difference between groups in functional decline. Both study groups experienced a significant decline in function over 18 months. The current study proposes to test a home-based intervention specifically designed to slow the rate of functional decline among older adults with Alzheimer's disease. In addition to building on our past research, the study also builds from recently reported research which demonstrated the short-term efficacy of home-based occupational therapy interventions among older adults with dementia. These trials show that older adults with dementia, including Alzheimer's disease, can both participate in and benefit from occupational therapy-based interventions delivered in the home. The specific aim of this study is to conduct a two-year, randomized, controlled clinical trial to improve functioning among older adults with Alzheimer's disease by comparing a control group receiving best practices primary care with an intervention group receiving best practice primary care plus a home-based occupational therapy intervention. We will test the primary hypothesis that subjects with Alzheimer's disease in the intervention group will have improved function at two years compared with the best practice primary care control group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer's Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
180 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Best practices primary care
Arm Type
Active Comparator
Arm Description
Best practices primary care encompasses the collaborative care intervention tested in a prior clinical trial (Callahan CM et al. JAMA 2006).
Arm Title
Home based occupational therapy
Arm Type
Experimental
Arm Description
The intervention group receives all of the components of best practice primary care in addition to a home-based intervention designed to slow functional decline.
Intervention Type
Behavioral
Intervention Name(s)
Home based occupational therapy
Intervention Description
An occupational therapist (OT) will deliver the home-based intervention. There are three cycles of intervention over two years, with each cycle delivering eight 60-90 minute home sessions. Cycle one takes place over 16 weeks, cycle two over 32 weeks, and cycle three over one year. Telephone calls take place in intervening weeks, with additional phone calls allowed to assist with problem solving and interval problems. At minimum, the OT will perform an assessment at the beginning of each cycle in order to tailor the home based component for individual dyads at each cycle. The OT will collaborate with the patients and caregivers to develop client centered goals with "homework" each week in order to encourage carryover of strategies, home environmental modifications, or home exercise programs.
Intervention Type
Behavioral
Intervention Name(s)
Best practices primary care
Intervention Description
Collaborative care is provided by an advanced practice nurse working in collaborations with a family caregiver, the primary care physician, and geriatric medicine specialists. Caregivers complete a formal assessment of problematic behaviors to assess current symptoms and stressors, and the care manager makes recommendations based on these results and using standardized protocols. Protocols focus first on non-pharmacologic interventions. If these interventions fail, the care manager collaborates with the primary care physician and/or specialists to institute protocol-based drug therapy or other strategies. Patients and caregivers are also offered access to support groups.
Primary Outcome Measure Information:
Title
Alzheimer's Disease Cooperative Study Activities of Daily Living Inventory (ADCS - ADLI)
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Short Physical Performance Battery (SPPB)
Description
Includes Side by Side Stand, Semi-Tandem Stand, Tandem Stand, Repeated Chair Stands, and 3 or 4 meter walk
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Tandem Stand, eyes closed
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
One Leg Stand, eyes open
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Mini Mental State Examination
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Word List Learning
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Delayed Word List Recall
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Grip Strength
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Neuropsychiatric Inventory (NPI)
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Alzheimer's Disease Cooperative Studies Resource Use Scale
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
PHQ - 9
Description
Depression
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
GAD - 7
Description
Anxiety
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Comorbid Conditions
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months
Title
Adverse Events
Time Frame
Baseline, 6 months, 12 months, 18 months, and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Patient Inclusion Criteria: Currently a patient within Wishard Health Services in Central Indiana Diagnosed with possible or probable Alzheimer's Disease Age 45 or older English speaking Hear well enough to answer questions in person or by telephone Community-dwelling (includes senior communities, but not skilled nursing facilities) Caregiver willing to participate in the study Willing to receive home visits Lives in Indianapolis metro area and planning to continue care at primary care clinic Caregiver Inclusion Criteria Age 18 or older English speaking Hear well enough to answer questions in person or by telephone Community-dwelling Willing to receive home visits Exclusion Criteria: Not a current patient within Wishard Health Services Does not speak English Currently enrolled in another study Non-community dwelling, or residing in a skilled nursing facility
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher M Callahan, MD
Organizational Affiliation
Indiana University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wishard Health Services
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16684985
Citation
Callahan CM, Boustani MA, Unverzagt FW, Austrom MG, Damush TM, Perkins AJ, Fultz BA, Hui SL, Counsell SR, Hendrie HC. Effectiveness of collaborative care for older adults with Alzheimer disease in primary care: a randomized controlled trial. JAMA. 2006 May 10;295(18):2148-57. doi: 10.1001/jama.295.18.2148.
Results Reference
background
PubMed Identifier
19689236
Citation
Callahan CM, Boustani M, Sachs GA, Hendrie HC. Integrating care for older adults with cognitive impairment. Curr Alzheimer Res. 2009 Aug;6(4):368-74. doi: 10.2174/156720509788929228.
Results Reference
background
PubMed Identifier
15331812
Citation
Guerriero Austrom M, Damush TM, Hartwell CW, Perkins T, Unverzagt F, Boustani M, Hendrie HC, Callahan CM. Development and implementation of nonpharmacologic protocols for the management of patients with Alzheimer's disease and their families in a multiracial primary care setting. Gerontologist. 2004 Aug;44(4):548-53. doi: 10.1093/geront/44.4.548.
Results Reference
background
PubMed Identifier
27893087
Citation
Callahan CM, Boustani MA, Schmid AA, LaMantia MA, Austrom MG, Miller DK, Gao S, Ferguson DY, Lane KA, Hendrie HC. Targeting Functional Decline in Alzheimer Disease: A Randomized Trial. Ann Intern Med. 2017 Feb 7;166(3):164-171. doi: 10.7326/M16-0830. Epub 2016 Nov 22.
Results Reference
derived
PubMed Identifier
22737979
Citation
Callahan CM, Boustani MA, Schmid AA, Austrom MG, Miller DK, Gao S, Morris CS, Vogel M, Hendrie HC. Alzheimer's disease multiple intervention trial (ADMIT): study protocol for a randomized controlled clinical trial. Trials. 2012 Jun 27;13:92. doi: 10.1186/1745-6215-13-92.
Results Reference
derived

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Alzheimer's Disease Multiple Intervention Trial

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