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Using Behavioral Programs to Treat Sleep Problems in Individuals With Alzheimer's Disease

Primary Purpose

Alzheimer Disease, Sleep Initiation and Maintenance Disorders

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Walking Program
Light Exposure Program
Combined Education, Walking and Light Exposure Program
Routine Medical Care with Education
Sponsored by
University of Washington
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer Disease focused on measuring Alzheimer's Disease, Insomnia, Sleep Problems, Elderly, Caregivers

Eligibility Criteria

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

Inclusion Criteria for Alzheimer's Disease Patients: Diagnosis of probable or possible Alzheimer's Disease Have at least two sleep disturbances, occurring 3 or more times per week Reside in a residential home with a family member caregiver Able to walk without assistance Exclusion Criteria for Alzheimer's Disease Patients: Pre-existing diagnosis of a primary sleep disorder, such as sleep apnea or periodic limb movement disorder Blindness Current use of photosensitizing medication Inclusion Criteria for Family Caregiver: Currently caring for a family member with Alzheimer's disease

Sites / Locations

  • University of Washington

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

1

2

3

4

Arm Description

Routine medical care with education: therapist provides information about the nature of sleep changes in people with Alzheimer's disease, general information about treatments for insomnia, and caregiver support.

Walking: the therapist introduces a walking program and assists the caregiver in establishing a daily walking routine of 30 minutes for the study participant.

Light exposure: the therapist provides a light box and teaches the caregiver how to use the box so that the study participant's daily exposure to bright light is one hour.

Combination: the therapist provides education plus assistance setting up an individualized sleep program, a daily walking routine, and a schedule for daily light exposure.

Outcomes

Primary Outcome Measures

Patient total wake time (actigraphy)
Caregiver reports of patient behavioral disturbances at night (Sleep Disorders Inventory)

Secondary Outcome Measures

Additional patient actigraphy outcomes
Patient daytime sleepiness, behavioral problems, and residential status
Caregiver sleep

Full Information

First Posted
September 13, 2005
Last Updated
January 12, 2012
Sponsor
University of Washington
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00183378
Brief Title
Using Behavioral Programs to Treat Sleep Problems in Individuals With Alzheimer's Disease
Official Title
Behavioral Treatment of Nocturnal Disturbances in Alzheimer's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
September 2009 (Actual)
Study Completion Date
March 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study will compare four different behavioral treatment programs to determine which is most effective in reducing night-time disturbances in individuals with Alzheimer's disease (AD).
Detailed Description
Nocturnal disturbances, such as getting out of bed repeatedly, having hallucinations, talking or singing in bed, and waking up confused are common among patients with AD. Such nocturnal disturbances are associated with increased physical and psychological morbidity in both AD patients and their caregivers and are a major risk factor for patient institutionalization. Nonpharmacologic treatments for these disturbances are needed. This study will assign AD patients to one of four different treatments to determine which is most effective in reducing nocturnal disturbances. This study will last 6 months. Participants will be randomly assigned to a walking program, a light exposure program, a "NITE-AD" program, combining the walking and light exposure programs, or routine AD care with nocturnal disturbance education. Walking program participants will have three 1-hour visits with a therapist over an 8-week period. The therapist and the participant will set an initial daily walking goal and develop a plan for gradually increasing the participants' walking to 30 minutes/day, to be increased at a participant-selected pace. Pedometers will be given to participants to monitor daily activity. The therapist will also discuss exercise safety and will review ways to prevent muscle soreness. Light program participants will also have three 1-hour visits with a therapist over 8 weeks. The therapist will develop a daily, caregiver-supervised light exposure plan requiring participants to sit in front of a light box for 1 hour every day. NITE-AD program participants will have six 1-hour visits with a therapist over 8 weeks; their visits will include setting up both walking and the light exposure routines. Participants assigned to education will receive information about about sleep in aging and dementia, but no assistance setting up walking or light exposure plans. Participants will be assessed at study entry and at Months 2 (post-test) and 6. The sleep patterns of both the patients and the caregivers will be measured. Caregiver reports of patients' night-time behavioral disturbances and readings from an actigraph, a small electronic device worn by participants that records and reports their levels of activity at night, will be used to estimate sleep. The study will also collect data on patient and caregiver mood, stress, and behavior. A follow-up visit will occur 6 months after study completion; at the follow-up visit, the same outcome measures will be collected as at baseline and post-test. Participants will receive 3 biannual phone follow-ups (12, 18, and 24 months) to assess patient residential status and caregiver reports of patient and caregiver sleep.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease, Sleep Initiation and Maintenance Disorders
Keywords
Alzheimer's Disease, Insomnia, Sleep Problems, Elderly, Caregivers

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
132 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Routine medical care with education: therapist provides information about the nature of sleep changes in people with Alzheimer's disease, general information about treatments for insomnia, and caregiver support.
Arm Title
2
Arm Type
Active Comparator
Arm Description
Walking: the therapist introduces a walking program and assists the caregiver in establishing a daily walking routine of 30 minutes for the study participant.
Arm Title
3
Arm Type
Active Comparator
Arm Description
Light exposure: the therapist provides a light box and teaches the caregiver how to use the box so that the study participant's daily exposure to bright light is one hour.
Arm Title
4
Arm Type
Active Comparator
Arm Description
Combination: the therapist provides education plus assistance setting up an individualized sleep program, a daily walking routine, and a schedule for daily light exposure.
Intervention Type
Behavioral
Intervention Name(s)
Walking Program
Intervention Description
The therapist introduces a walking program and assists the caregiver in establishing a walking routine of 30 minutes/day for the study participant.
Intervention Type
Behavioral
Intervention Name(s)
Light Exposure Program
Intervention Description
The therapist provides a light box and teaches the caregiver how to use the box so that the study participant's daily exposure to bright light is one hour.
Intervention Type
Behavioral
Intervention Name(s)
Combined Education, Walking and Light Exposure Program
Intervention Description
The therapist provides a combination of education plus assistance setting up an individualized sleep program, a daily walking routine, and a schedule for daily light exposure.
Intervention Type
Behavioral
Intervention Name(s)
Routine Medical Care with Education
Intervention Description
The therapist provides information about the nature of sleep changes in people with Alzheimer's disease, general information about treatments for insomnia, and caregiver support. Participants are free to use whatever medical services they wish during study participation.
Primary Outcome Measure Information:
Title
Patient total wake time (actigraphy)
Time Frame
Measured 3 times over 6 months
Title
Caregiver reports of patient behavioral disturbances at night (Sleep Disorders Inventory)
Time Frame
Measured 3 times over 6 months
Secondary Outcome Measure Information:
Title
Additional patient actigraphy outcomes
Time Frame
Measured 3 times over 6 months
Title
Patient daytime sleepiness, behavioral problems, and residential status
Time Frame
Measured 3 times over 6 months
Title
Caregiver sleep
Time Frame
Measured 3 times over 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria for Alzheimer's Disease Patients: Diagnosis of probable or possible Alzheimer's Disease Have at least two sleep disturbances, occurring 3 or more times per week Reside in a residential home with a family member caregiver Able to walk without assistance Exclusion Criteria for Alzheimer's Disease Patients: Pre-existing diagnosis of a primary sleep disorder, such as sleep apnea or periodic limb movement disorder Blindness Current use of photosensitizing medication Inclusion Criteria for Family Caregiver: Currently caring for a family member with Alzheimer's disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Susan M. McCurry, PhD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
14511168
Citation
McCurry SM, Gibbons LE, Logsdon RG, Vitiello M, Teri L. Training caregivers to change the sleep hygiene practices of patients with dementia: the NITE-AD project. J Am Geriatr Soc. 2003 Oct;51(10):1455-60. doi: 10.1046/j.1532-5415.2003.51466.x.
Results Reference
background
PubMed Identifier
15877554
Citation
McCurry SM, Gibbons LE, Logsdon RG, Vitiello MV, Teri L. Nighttime insomnia treatment and education for Alzheimer's disease: a randomized, controlled trial. J Am Geriatr Soc. 2005 May;53(5):793-802. doi: 10.1111/j.1532-5415.2005.53252.x.
Results Reference
background
PubMed Identifier
20660515
Citation
McCurry SM, Pike KC, Logsdon RG, Vitiello MV, Larson EB, Teri L. Predictors of short- and long-term adherence to a daily walking program in persons with Alzheimer's disease. Am J Alzheimers Dis Other Demen. 2010 Sep;25(6):505-12. doi: 10.1177/1533317510376173. Epub 2010 Jul 26.
Results Reference
result
PubMed Identifier
21797835
Citation
McCurry SM, Pike KC, Vitiello MV, Logsdon RG, Larson EB, Teri L. Increasing walking and bright light exposure to improve sleep in community-dwelling persons with Alzheimer's disease: results of a randomized, controlled trial. J Am Geriatr Soc. 2011 Aug;59(8):1393-402. doi: 10.1111/j.1532-5415.2011.03519.x. Epub 2011 Jul 28.
Results Reference
result

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Using Behavioral Programs to Treat Sleep Problems in Individuals With Alzheimer's Disease

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