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Remote research study to develop measurement technologies

Remote research study to develop measurement technologies

The goal is to develop measurement technologies that can help improve clinical trials for ataxias.

 

About the Study

Eligible Ataxia Types
Spinocerebellar Ataxias and Multiple System Atrophy

Type of Study
Research Study

Clinical Trial Phase
N/A

Age Range
Adult 18+

Study Start Date
11/2020

Estimated Completion Date
N/A – Ongoing

IRB Approval #
2019P003458

Location(s)

Massachusetts General Hospital
Remote Study

Contact Information

Rohin Manohar
rmanohar@mgh.harvard.edu
Phone: 617-726-7909

What does participation in the study entail?

No in-person visits are necessary. Participants will be asked to wear a wrist and ankle device continuously for one week, complete a speech survey and a computer mouse task twice per week for 2 weeks, and complete quality of life surveys. Participants will be asked to complete similar study tasks every 6 months for up to 3 years.

What are the potential benefits for participants?

This study will help develop measurement tools to improve clinical trials in ataxias. 

What are the potential risks for participants?

As with all studies conducted online, there is a potential for a security breach of collected data and confidentially, but we take any and all precautions to protect collected data.

Is there financial compensation?

Yes. $50-$300. Participants will receive $50 for each time they participate in the study. 

Is there travel reimbursement?

No

Who is eligible?

Adults who have been diagnosed with spinocerebellar ataxia, have a family history of ataxia, multiple system atrophy, or healthy volunteers. You are eligible to participate even if you do not have any symptoms. We want to develop tools that can detect and measure the earliest signs of ataxia.

View Other Research Opportunities

PRIME-Ataxia RCT

This study aims to determine the feasibility and efficacy of an 8-week remote intervention of high intensity aerobic exercise prior to balance training compared to an 8-week remote intervention low Read More…

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Read More »
Print Friendly, PDF & Email

The goal is to develop measurement technologies that can help improve clinical trials for ataxias.

 

About the Study

Eligible Ataxia Types
Spinocerebellar Ataxias and Multiple System Atrophy

Type of Study
Research Study

Clinical Trial Phase
N/A

Age Range
Adult 18+

Study Start Date
11/2020

Estimated Completion Date
N/A – Ongoing

IRB Approval #
2019P003458

Location(s)

Massachusetts General Hospital
Remote Study

Contact Information

Rohin Manohar
rmanohar@mgh.harvard.edu
Phone: 617-726-7909

What does participation in the study entail?

No in-person visits are necessary. Participants will be asked to wear a wrist and ankle device continuously for one week, complete a speech survey and a computer mouse task twice per week for 2 weeks, and complete quality of life surveys. Participants will be asked to complete similar study tasks every 6 months for up to 3 years.

What are the potential benefits for participants?

This study will help develop measurement tools to improve clinical trials in ataxias. 

What are the potential risks for participants?

As with all studies conducted online, there is a potential for a security breach of collected data and confidentially, but we take any and all precautions to protect collected data.

Is there financial compensation?

Yes. $50-$300. Participants will receive $50 for each time they participate in the study. 

Is there travel reimbursement?

No

Who is eligible?

Adults who have been diagnosed with spinocerebellar ataxia, have a family history of ataxia, multiple system atrophy, or healthy volunteers. You are eligible to participate even if you do not have any symptoms. We want to develop tools that can detect and measure the earliest signs of ataxia.

View Other Research Opportunities

PRIME-Ataxia RCT

This study aims to determine the feasibility and efficacy of an 8-week remote intervention of high intensity aerobic exercise prior to balance training compared to an 8-week remote intervention low Read More…

Print Friendly, PDF & Email
Read More »
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