Two Interventions for Early Stage Dementia: A Comparative Efficacy Trial
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Purpose
Alzheimer's disease (AD) is increasing exponentially, with a projected quadrupling of cases by the mid 21st century. Individuals with AD are at increased risk for a host of medical and psychiatric conditions, and evidence is accumulating supporting the efficacy and effectiveness of psychosocial interventions for improving their mood, function, health, and quality of life. Such interventions are likely to be most effective when they are implemented during the early stages of dementia, when individuals and their family members are coping with the initial diagnosis and associated changes in abilities and activities. Recent randomized clinical trials by the Principal Investigator and colleagues have developed two non-pharmacologic interventions to reduce the social, psychological, physical, and behavioral impact of dementia. This investigation is focused on facilitating their translation into ongoing community-based programs, such as those provided by Alzheimer's Association chapters, senior centers, retirement homes, and other health care providers. The core content of each intervention has been retained in order to maintain or improve their efficacy, and each has been modified to a 4-week group format to increase efficiency of delivery. These modified interventions (ESML-Social and ESML-Ex) will be compared to each other and to a usual care (UC) control group. Outcomes will be assessed at baseline, 1-month post treatment, and 4 month follow-up. Primary outcomes at the 1-month assessment include: social activity participation, family communication, physical activity participation, and physical function. Primary outcomes at 4-month follow up include overall quality of life and depression. It is hypothesized that ESML-Ex and ESML-Social both will have greater improvements than UC. It is hypothesized that ESML-Social will have greater improvements in social participation and family communication than ESML-Ex and UC. It is hypothesized that ESML-Ex will have greater improvements in physical activity participation and physical functioning than ESML-Social and UC. If successful, these 4-week programs may be developed into "modules" that can be incorporated into programming for individuals with early stage dementia in a variety of community settings.
| Condition | Intervention |
|---|---|
|
Dementia |
Behavioral: ESML-EX (Physical Activity Program) Behavioral: ESML-Social (Social Activity Program) Behavioral: Usual Care Control |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Single Blind (Outcomes Assessor) Primary Purpose: Treatment |
| Official Title: | Two Interventions for Early Stage Dementia: A Comparative Efficacy Trial |
- Change from Baseline in Social Activity at post-treatment (1 month) [ Time Frame: Baseline and post treatment (1 month) ] [ Designated as safety issue: No ]The Pleasant Events Schedule-AD, long version, will be used to evaluate social participation and activity.
- Change from Baseline in Physical Activity at post-treatment (1 month) [ Time Frame: Baseline and post-treatment (1 month) ] [ Designated as safety issue: No ]The Physical Activity Scale for the Elderly (PASE) will be used to assess level of physical activity of participants and care partners.
- Change from Baseline in Quality of Life at post-treatment (1 month) [ Time Frame: Baseline and post treatment (1 month) ] [ Designated as safety issue: No ]The Quality of Life-AD (QOL-AD)scale will measure quality of life domains identified as important for cognitively impaired older adults.
- Change from Baseline in Social Activity at 4 month follow-up [ Time Frame: Baseline and 4 month follow-up ] [ Designated as safety issue: No ]The Pleasant Events Schedule-AD, long version, will be used to evaluate social participation and activity.
- Change from Baseline in Physical Activity at 4 month follow-up [ Time Frame: Baseline and 4 month follow-up ] [ Designated as safety issue: No ]The Physical Activity Scale for the Elderly (PASE) will be used to assess level of physical activity of participants and care partners.
- Change from Baseline in Quality of Life at 4 month follow-up [ Time Frame: Baseline and 4 month follow-up ] [ Designated as safety issue: No ]The Quality of Life-AD (QOL-AD)scale will measure quality of life domains identified as important for cognitively impaired older adults.
- Change from Baseline in Communication at post-treatment (1 month) [ Time Frame: Baseline and post treatment (1 month) ] [ Designated as safety issue: No ]The Communication, Affective Expression, and Involvement subscales of the Family Assessment Measure will measure the quality of caregiver-patient communication.
- Change from Baseline in Physical Function at post-treatment (1 month) [ Time Frame: Baseline and post treatment (1 month) ] [ Designated as safety issue: No ]The Physical Functioning Scale rates the performance of everyday tasks such as walking around the residence and getting in and out of bed.
- Change from Baseline in Mood at post-treatment (1 month) [ Time Frame: Baseline and post-treatment (1 month) ] [ Designated as safety issue: No ]The Geriatric Depression Scale will assess the mood of the participant and their caregiver.
- Change from Baseline in Communication at post-treatment (1 month) [ Time Frame: Baseline and post-treatment (1 month) ] [ Designated as safety issue: No ]The Communication, Affective Expression, and Involvement subscales of the Family Assessment Measure will measure the quality of caregiver-patient communication.
- Change from Baseline in Physical Functioning at post-treatment (1 month) [ Time Frame: Baseline and post-treatment (1 month) ] [ Designated as safety issue: No ]The Physical Functioning Scale rates the performance of everyday tasks such as walking around the residence and getting in and out of bed.
- Change from Baseline in Mood at 4 month follow-up. [ Time Frame: Baseline and 4 month follow-up ] [ Designated as safety issue: No ]The Geriatric Depression Scale will assess the mood of the participant and their caregiver.
| Estimated Enrollment: | 240 |
| Study Start Date: | February 2012 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | December 2013 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: ESML-EX (Physical Activity Program)
ESML-EX consists of four weekly 90-minute classes. Each class includes exercises and a brief discussion of a specific health topic. Classes are carried out in small groups of five to six participant/care partner dyads (10-12 people total), to ensure everyone in the class gets individual attention and that all exercises are done safely using proper form.
|
Behavioral: ESML-EX (Physical Activity Program)
ESML-EX consists of four weekly 90-minute classes. Each class includes exercises and a brief discussion of a specific health topic.
|
|
Active Comparator: ESML-SOCIAL (Social Activity Program)
ESML-SOCIAL consists of four weekly 90-minute seminars. Each seminar includes discussion of a specific topic, open time for socializing, and a "homework" assignment to be completed prior to the next session. Seminars are carried out in small groups of five to six participant/care partner dyads (10-12 people total), to ensure everyone in the seminar gets individual attention and that everyone has a chance to bring up any concerns.
|
Behavioral: ESML-Social (Social Activity Program)
ESML-SOCIAL consists of four weekly 90-minute seminars. Each seminar includes discussion of a specific topic, open time for socializing, and a "homework" assignment to be completed prior to the next session.
|
|
No Intervention: Usual Care Control (UC)
This group will receive no intervention during the active phase of the study. After the final 4 month follow-up interview, participants in this group will be offered the opportunity to enroll in either of the active interventions-ESML-EX or ESML-Social.
|
Behavioral: Usual Care Control
This group will not receive an intervention during the active phase of the study.
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Dementia diagnosis
- Clinical Dementia Rating Scale score
- Care Partner agrees to participate with care recipient
- Care recipient lives in the community or a retirement home
- Both care partner and recipient speak English
Exclusion Criteria:
- Significant physical or psychiatric illness in either care partner or care recipient that would prevent participant in a exercise program
- Planning to move out of study area during the 4 month follow-up period
Contacts and Locations| Contact: Amy Moore, M.S. | 206-616-5550 | amoore@u.washington.edu |
| United States, Washington | |
| UWashington | Recruiting |
| Seattle, Washington, United States, 98195 | |
| Principal Investigator: | Rebecca G Logsdon, Ph.D. | University of Washington |
More Information
No publications provided
| Responsible Party: | Rebecca Logsdon, Research Professor, University of Washington |
| ClinicalTrials.gov Identifier: | NCT01550718 History of Changes |
| Other Study ID Numbers: | 41577-G |
| Study First Received: | March 5, 2012 |
| Last Updated: | March 7, 2012 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of Washington:
|
Aerobic Exercise Alzheimer's Disease Burden and Stress |
Caregiving Issues Quality of Life Early Stage Memory Loss |
Additional relevant MeSH terms:
|
Dementia Brain Diseases Central Nervous System Diseases |
Nervous System Diseases Delirium, Dementia, Amnestic, Cognitive Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 19, 2013