The Ohio State University
Columbus, Ohio, 43210, United States
NCT Number: NCT05270681
The purpose of this study is to determine if a movement to music exercise program delivered via telehealth is feasible and safe for individuals with neurodegenerative disease and their caregivers (Aim 1). A secondary aim will be to determine if a movement to music exercise program delivered via telehealth improves balance, cognition, mobility, and quality of life (Aim 2).
Looking for future studies?
Notify Me21 year and older
All sexes
Interventional
Not applicable
Columbus, Ohio, 43210, United States
The purpose of this study is to determine if a movement to music exercise program created for our clinic patients, called "Move to Improve," delivered via telehealth is possible and safe for individuals with neurodegenerative disease. Investigators also hope to determine if this telehealth movement to music exercise program improves balance, cognition, mobility, and quality of life. Participants will be asked to participate in a movement to music exercise program that will be accessible by video twice a week for 12 weeks and complete assessments before starting and after completing the program. Participants will be recruited from the OSU Neurology Clinic which serves a large regional area, including rural Appalachian counties. Participants will be ages 21 or older with a confirmed diagnosis of a degenerative neurologic disorder such as Huntington's disease who can access a computer, tablet, or smartphone, can complete the exercises, and have a care partner. Participants will be educated on how to access prerecorded Move to Improve classes conducted by a professional dance instructor which are accessible by computer or tablet 24/7 via a hyperlink. This link will be accessible to the community. Here is a link to an example of the class lead by the instructor for this study: https://www.youtube.com/watch?v=NdoPi9YXoWg. Classes last 45 minutes, and participants will be instructed to participate in the activity at least twice weekly, for 12 weeks. Each class uses movement to music combinations across different dance genres that build in intensity and sequence complexity, accompanied by music with faster beats, to encourage participants to achieve a moderate-vigorous level of physical and cognitive activity. Care givers will be also participate in the exercise class and will be present to ensure safety. The care giver and participant will be instructed to stand at a counter or behind a chair for safety during exercise. Participants within driving distance will come to the MEND lab for in-person outcome measures at baseline and after the 12 week intervention. Assessments will also be administered to all participants via telehealth. For those individuals who are not able to come to the lab for assessment due to distance or other reasons, tests will only be administered via telehealth. These individuals will be consented via phone. Telehealth exercise classes will be conducted using a virtual meeting platform such as Zoom, Microsoft Teams, or FaceTime. Caregivers will be present during all assessments to ensure safety.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will be educated on how to access prerecorded Move to Improve classes conducted by a professional dance instructor which will be accessible by computer or tablet 24/7 via a hyperlink. Classes last 45 minutes, and participants will be instructed to participate in the activity at least twice weekly, for 12 weeks. Each class uses movement to music combinations across different dance genres that build in intensity and sequence complexity, accompanied by music with faster beats, to encourage participants to achieve a moderate-vigorous level of physical and cognitive activity. Care partners will be present during each class to ensure safety and will also participate in the Move to Improve exercise program. The care partner and participant will be instructed to stand at a counter or behind a chair for safety during exercise.
Time frame: 12 weeks
How long a participant can stand with feet together up to 10 seconds
Time frame: 12 weeks
How long a participant can stand with feet together up to 10 seconds collected via telehealth
Time frame: 12 weeks
How long a participant can stand with feet staggered up to 10 seconds
Time frame: 12 weeks
How long a participant can stand with feet staggered up to 10 seconds collected via telehealth
Time frame: 12 weeks
How long a participant can stand with feet heel to toe up to 10 seconds
Time frame: 12 weeks
How long a participant can stand with feet heel to toe up to 10 seconds collected via telehealth
Time frame: 12 weeks
How long a participant can stand on one foot to toe up to 60 seconds
Time frame: 12 weeks
How long a participant can stand on one foot to toe up to 60 seconds collected via telehealth
Time frame: 12 weeks
How long a participant can stand up and sit down from a standard chair with arms crossed across chest in seconds
Time frame: 12 weeks
How long a participant can stand up and sit down from a standard chair with arms crossed across chest in seconds collected via telehealth
Time frame: 12 weeks
A patient-reported outcome measure that assesses perceived difficulty in completing physical tasks.
Time frame: 12 weeks
A self-administered instrument for depression module, which scores each of the items as "0" (not at all) to "3" (nearly every day), with higher scores indicating worse depression
Time frame: 12 weeks
A self-administered instrument for depression module, which scores each of the items as "0" (not at all) to "3" (nearly every day), with higher scores indicating worse depression. Collected via telehealth
Time frame: 12 weeks
A patient reported outcome measure containing 12 items that the participant rates his or her difficulties in maintaining personal care, occupational tasks and functioning in relation to family and society with a score range from 12 to 60, where higher scores indicate higher disability or loss of function.
Time frame: 12 weeks
A patient reported outcome measure containing 12 items that the participant rates his or her difficulties in maintaining personal care, occupational tasks and functioning in relation to family and society with a score range from 12 to 60, where higher scores indicate higher disability or loss of function. Collected via telehealth
Time frame: 12 weeks
A measure of cognition that involves asking the participant to name as many animals as they can in 60 seconds and then they are given a letter and asked to name all of the words that begin with that letter in 60 seconds. The more words the better the outcome.
Time frame: 12 weeks
A measure of cognition that involves asking the participant to name as many animals as they can in 60 seconds and then they are given a letter and asked to name all of the words that begin with that letter in 60 seconds. The more words the better the outcome. Collected via telehealth.
Time frame: 12 weeks
A measure of cognition that involves asking the participant to recall a series of numbers. The more numbers recalled accurately the better the outcome.
Time frame: 12 weeks
A measure of cognition that involves asking the participant to recall a series of numbers. The more numbers recalled accurately the better the outcome. Collected via telehealth
Time frame: 12 weeks
UHDRS Motor Scale is administered by a trained rater who has the individual perform tasks such as tapping fingers and standing up and walking. The rater then scores performance on a scale of 0-4. Higher scores indicates worse outcomes
Time frame: 12 weeks
A questionnaire that participants fill out rating their difficulty dealing with life situations on a yes or no scale
Time frame: 12 weeks
A questionnaire that participants fill out rating their difficulty performing tasks on a scale of 10-100 with 100 indicating independence
Time frame: 12 weeks
The SDMT is a part of the standard cognitive battery used with Huntington's disease that involves a simple substitution task, using a reference key, the examinee has 90 seconds to pair specific numbers with given geometric figures.
Time frame: 12 weeks
The Stroop is a part of the standard cognitive battery used with Huntington's disease that involves participants to read three different tables as fast as possible. Two of them represent the "congruous condition" in which participants are required to read names of colors (henceforth referred to as color-words) printed in black ink (W) and name different color patches (C). Conversely, in the third table, named color-word (CW) condition, color-words are printed in an inconsistent color ink (for instance the word "red" is printed in green ink).
Time frame: 12 weeks
A survey to describe participant perceptions about the intervention at the end of the study
Ohio State University
Other
Move to Improve: Telehealth Exercise and Music Intervention for Individuals With Huntington's Disease
Acronym: MtI
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT05250323
Basal Ganglia Diseases, Behavior
Burgos, Spain
View Trial DetailsNCT02268617
Basal Ganglia Diseases, Behavior
Columbus, Ohio, United States
View Trial DetailsNCT06667414
Basal Ganglia Diseases, Brain Diseases
Birmingham, Alabama, United States
View Trial DetailsNCT05157074
Basal Ganglia Diseases, Behavior
Baltimore, Maryland, United States
View Trial Details