- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02398149
Characterizing Upper Extremity Function in Individuals With Multiple Sclerosis
August 28, 2017 updated by: Jennifer Ruiz, DPT, Mount Sinai Rehabilitation Hospital
Upper extremity (UE) function is critical to maintaining independence.
Better understanding of UE involvement in MS will provide necessary information to prioritize the design and selection of future interventions.
The goal of the proposed project is to characterize UE involvement in a population of community-based persons with MS across the International Classification of Functioning, Disability & Health (ICF) domains and constructs.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
267
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Connecticut
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Hartford, Connecticut, United States, 06112
- Mandell Center for Multiple Sclerosis at the Mount Sinai Rehabilitation Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Persons with MS who receive care at the Mandell Center for Multiple Sclerosis.
Description
Inclusion Criteria:
- Confirmed clinical Clinical diagnosis of MS
- Receive MS care at the Mandell MS Center
- Cognitively able to understand directions and complete protocol
- Signed consent form approved by the Saint Francis Institutional Review Board
- 18 years of age or older
Exclusion Criteria:
- Unwilling or unable to complete assessments
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
|---|
|
PwMS receiving care at the Mandell Center
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Prevalance of Impairment in the Upper Extremity
Time Frame: 3hours
|
3hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2013
Primary Completion (Actual)
October 1, 2016
Study Completion (Actual)
October 1, 2016
Study Registration Dates
First Submitted
March 2, 2015
First Submitted That Met QC Criteria
March 19, 2015
First Posted (Estimate)
March 25, 2015
Study Record Updates
Last Update Posted (Actual)
August 30, 2017
Last Update Submitted That Met QC Criteria
August 28, 2017
Last Verified
August 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 13-12-002-E
- RG 4815A2/2 (Other Grant/Funding Number: National Multiple Sclerosis Society)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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