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Dance Classes for Alzheimer's Disease (IGROOVE Trial)
N/A
Recruiting
Led By Christina Hugenschmidt, PhD
Research Sponsored by Wake Forest University Health Sciences
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, month 1, month 3, month 6
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing whether dancing can help improve memory for older adults, and how often it needs to be done to be effective.
Who is the study for?
This trial is for people aged 65+ who are worried about memory loss but don't have cognitive impairment. They must speak English, be low-active, able to do exercise tests, and have a MoCA score ≥21. Participants need reliable transport (provided if necessary) and must be MRI compatible.
What is being tested?
The study examines how dance movement and music appreciation classes affect memory and fitness in older adults at risk for Alzheimer's. Over six months, participants will attend either one, two or three weekly classes alongside clinical assessments including brain MRIs.
What are the potential side effects?
Since the interventions involve non-invasive activities like dance and music classes, side effects may include typical physical activity-related issues such as muscle soreness or fatigue. However, specific risks related to these activities aren't detailed.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, month 1, month 3, month 6
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, month 1, month 3, month 6
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Peak Oxygen Consumption (VO2)
Repeatable Battery for the Assessment of Neuropsychological Status (RBANS)
Secondary study objectives
Class Attendance
Exercise Self-Efficacy
Other study objectives
Average Heart Rate
Brief Psychological Needs Satisfaction and Frustration Scale (BPNSFS)--Frustration
Brief Psychological Needs Satisfaction and Frustration Scale (BPNSFS)--Satisfaction
+7 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
4Treatment groups
Experimental Treatment
Active Control
Group I: Dance 3 Times Weekly (3xD)Experimental Treatment1 Intervention
Participants in this arm will attend classes 3 times a week for 24 weeks. During the 24 weeks, four different dance forms will be practiced. Each dance form will be taught for 6 weeks.
Group II: Dance 2 Times Weekly (2xD)Experimental Treatment1 Intervention
Participants in this arm will attend classes 2 times a week for 24 weeks. During the 24 weeks, four different dance forms will be practiced. Each dance form will be taught for 6 weeks.
Group III: Dance 1 Time Weekly (1xD)Experimental Treatment1 Intervention
Participants in this arm will attend a class 1 time a week for 24 weeks. During the 24 weeks, four different dance forms will be practiced. Each dance form will be taught for 6 weeks.
Group IV: Music Appreciation Classes (MAC)Active Control1 Intervention
In the MAC, the music associated with that dance form will be used as the subject for classes and will also change every 6 weeks.
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Who is running the clinical trial?
National Institute on Aging (NIA)NIH
1,802 Previous Clinical Trials
28,193,821 Total Patients Enrolled
Wake Forest University Health SciencesLead Sponsor
1,401 Previous Clinical Trials
2,460,145 Total Patients Enrolled
Christina Hugenschmidt, PhDPrincipal InvestigatorWake Forest University Health Sciences
2 Previous Clinical Trials
116 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am not on any medication that could harm me during the trial.My current health does not impact my thinking, movement, or ability to attend study visits.I have been diagnosed with a major neurological disorder.I have long-term dizziness.I have had hip or knee surgery, or spinal surgery in the last 6 months.You are able to travel to the study site.I do not have severe high blood pressure, very high triglycerides, uncontrolled diabetes, or anemia.My cognitive function score is 21 or higher.My thinking and memory skills are normal.I cannot or do not want to attend weekly classes 1-3 times.I can speak English.I understand and can follow the study's procedures.I have had a stroke that affects my brain function or symptoms.You are willing and able to perform physical exercise tests.
Research Study Groups:
This trial has the following groups:- Group 1: Dance 1 Time Weekly (1xD)
- Group 2: Dance 2 Times Weekly (2xD)
- Group 3: Dance 3 Times Weekly (3xD)
- Group 4: Music Appreciation Classes (MAC)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Alzheimer's Disease Patient Testimony for trial: Trial Name: NCT05507905 — N/A