Social Dance Therapy for Early Alzheimer's Disease
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores how social dance therapy might benefit individuals with early Alzheimer's disease. Researchers believe that combining movement and mental activity, as in dance, could enhance both physical and mental abilities. Participants will join either a dance class or a walking group (known as WALK) to determine which activity better supports brain health and overall function. The trial seeks individuals with mild memory issues who can walk unaided and are not currently in an exercise program. As an unphased trial, this study offers a unique opportunity to explore innovative therapies that could enhance quality of life.
Will I have to stop taking my current medications?
The trial requires that participants are not on medications that could negatively affect cognition, such as antipsychotics, opioids, stimulants, and certain drugs for Parkinson's and multiple sclerosis. Participants must also be on stable doses of medications like Aricept or Namenda for at least 3 months before joining the study.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Studies have shown that partnered rhythmic rehabilitation (PRR) classes are safe for people with early Alzheimer's, with no reports of falls causing injury during sessions. PRR involves dancing with a partner, which helps improve both physical movement and thinking skills.
Research indicates that group walking programs can support brain health and physical function in older adults, including those with Alzheimer's. Walking is generally considered a safe and beneficial exercise.
Both treatments seem well-tolerated in similar settings, with no major safety concerns reported.12345Why are researchers excited about this trial?
Researchers are excited about these treatments for early Alzheimer's disease because they offer a non-pharmacological approach that could complement or even enhance existing therapies like medications that target neurotransmitter activity. Unlike standard drugs, which often aim to modify brain chemistry, Partnered Rhythmic Rehabilitation (PRR) and group walking (WALK) focus on physical activity and social engagement, which could improve cognitive function and quality of life. PRR is particularly unique as it incorporates music and rhythm, potentially stimulating brain areas involved in movement and memory. These treatments are exciting because they could provide holistic benefits without the side effects typically associated with medication.
What evidence suggests that this trial's treatments could be effective for early Alzheimer's disease?
Research has shown that walking in groups, one of the interventions in this trial, can help maintain mental stability in people with Alzheimer's disease. Studies have found that regular walking may slow the disease's progression and assist with daily activities. Participants in walking programs often maintain their quality of life over time.
Partnered Rhythmic Rehabilitation (PRR), another intervention in this trial, shows promise for enhancing the coordination of brain and body functions in older adults with memory issues. Early findings suggest that PRR, which combines physical activity with mental tasks in a social setting, may improve both cognitive and motor skills. This approach targets several areas, including heart health and social interaction, which are crucial for individuals in the early stages of Alzheimer's.678910Who Is on the Research Team?
Madeleine Hackney, MD
Principal Investigator
Emory University
Are You a Good Fit for This Trial?
This trial is for individuals with early Alzheimer's Disease who can walk unaided, have a certain level of cognitive function and memory concern, completed at least six grades of education or have a solid work history, are not very physically active, and willing to commit to a year-long research program. Those with severe mental health issues, recent hospitalization or conditions that could interfere with the study cannot participate.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Training
Participants are assigned to 20 biweekly 90-minute lessons over 12 weeks, focusing on either PRR or WALK interventions.
Maintenance
Participants attend weekly lessons at least 3 times per month for 9 months, continuing with either PRR or WALK interventions.
Follow-up
Participants are monitored for safety and effectiveness after the intervention period.
What Are the Treatments Tested in This Trial?
Interventions
- Group walking (WALK)
- Partnered Rhythmic Rehabilitation (PRR)
Trial Overview
The trial tests Partnered Rhythmic Rehabilitation (PRR), which is social dance aimed at improving cardiovascular health, motor-cognitive functions and social interaction against group walking. It's a 12-month Phase II trial where participants do biweekly sessions for three months followed by weekly sessions for nine months.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Participants in this study are will receive the PRR intervention. Participants will have two phases of intervention. In the three-month Training phase, participants will be assigned to 20, biweekly (90-minute) lessons over 12 weeks. In the nine-month Maintenance phase, participants will attend weekly lessons at least 3 times per month.
Participants in this study are will receive the WALK intervention. Participants will have two phases of intervention. In the three-month Training phase, participants will be assigned to 20, biweekly (90-minute) lessons over 12 weeks. In the nine-month Maintenance phase, participants will attend weekly lessons at least 3 times per month.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Emory University
Lead Sponsor
National Institute on Aging (NIA)
Collaborator
Published Research Related to This Trial
Citations
Effectiveness of a group‐walking intervention for people with ...
This study showed that a group‐walking intervention over a 28‐week period for people with dementia held the quality of life stable over all seasons and the ...
Walking stabilizes cognitive functioning in Alzheimer's disease ...
In people with dementia, several studies support a possible role of physical activity on improved cognitive function, slowed disease course and improved ADL ( ...
Walking stabilizes cognitive functioning in Alzheimer's ...
Our results demonstrated that the patients spent little time engaged in physical activity in general, their overall activity levels decreased over time, and ...
High-intensity walking in midlife is associated with improved ...
A plenty of studies have shown sustained cognitive decline in episodic memory across longitudinal AD trajectories that includes preclinical, ...
Group-Based Exercise as a Therapeutic Strategy for the ...
The present study's eight-week, low-cost, group-based exercise program resulted in a 10.89% improvement in MMSE scores, which agrees with the findings of ...
Six-Month Walking Program Changes Cognitive and ADL ...
The aim of this study was to determine whether a walking program could reduce the functional and cognitive decline of elderly nursing home residents in the ...
Implementation and evaluation of a community-based mindful ...
This study commits to sustaining cognitive health among AA older adults by developing and implementing a mindful walking intervention to serve ...
Effects of intensive lifestyle changes on the progression of ...
Comprehensive lifestyle changes may significantly improve cognition and function after 20 weeks in many patients with MCI or early dementia due to AD.
Effects of Nordic walking in Alzheimer's disease: A single ...
Our study aimed to evaluate the effects of 24-week NW training on cognitive function in patients with mild/moderate AD to implement therapeutic strategies for ...
10.
frontiersin.org
frontiersin.org/journals/aging-neuroscience/articles/10.3389/fnagi.2023.1243869/fullExercise therapy to prevent and treat Alzheimer's disease
Aerobic exercise (with an intensity of 50–75% of VO2 max) prevents hippocampal volume reduction, spatial memory reduction, and learning reduction.
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