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Multiple Sclerosis clinical trials

View clinical trials related to Multiple Sclerosis.

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NCT ID: NCT02377323 Completed - Multiple Sclerosis Clinical Trials

Real-Life Outcomes of Multiple Sclerosis Treatment With Rebif

RLO
Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Rebif has an impact on employment status, quality of life and cognition.

NCT ID: NCT02373098 Completed - Clinical trials for Relapsing Remitting Multiple Sclerosis

Fingolimod Effect on Cytokine and Chemokine Levels

Start date: March 31, 2015
Phase: Phase 4
Study type: Interventional

The main purpose of this study was to measure the serum levels of cytokines and chemokines that are known to increase during multiple sclerosis relapses. Cytokines are a broad and loose category of small proteins that are important in cell signaling. The second purpose of the study was to test the cytokine/chemokine changes measured in the 3rd and 6th months on the efficacy parameters.

NCT ID: NCT02369224 Completed - Multiple Sclerosis Clinical Trials

Multicenter Validation of The Evergreen Myometric Strength Test for Lower Extremities (EMST-LE) in Multiple Sclerosis: Protocol for Strength Testing and Reliability Characteristics

EMST-LE
Start date: January 2015
Phase: N/A
Study type: Observational

A Cross- Sectional study; To assess the intra-rater and inter-rater reliability of a hand-held dynamometer (HHD) in the assessment of lower extremity strength in patients with multiple sclerosis

NCT ID: NCT02364505 Completed - Multiple Sclerosis Clinical Trials

A Telemedicine Mindfulness-based Intervention for People With Multiple Sclerosis and Their Caregivers

Start date: September 2014
Phase: N/A
Study type: Interventional

The aim of the project is to investigate the impact of a multiple sclerosis specific telemedicine mindfulness-based Intervention on the quality of life of people with multiple sclerosis and their caregivers.

NCT ID: NCT02346734 Completed - Multiple Sclerosis Clinical Trials

Physical Telerehabilitation in Veterans With Multiple Sclerosis

Start date: July 2012
Phase: N/A
Study type: Interventional

The primary objective of this study will be to assess the feasibility and patient acceptance of a Home Automated Telemanagement (HAT) system in multiple sclerosis patients. Our hypothesis is that home telemanagement will be effective and useful in the rehabilitation of multiple sclerosis patients. Specifically, the investigators hypothesize that home telemanagement using a daily exercise diary, monitoring of compliance with a tailored exercise program and regular assessment of strength and motor functions will: 1. Be feasible and acceptable in patients with multiple sclerosis 2. Improve patient compliance with home exercise program 3. Increase patient mobility and motor functions 4. Be a feasible and effective mechanism for affecting multiple sclerosis patient self-efficacy 5. Improve quality of life

NCT ID: NCT02346279 Completed - Multiple Sclerosis Clinical Trials

Responsiveness and Minimal Clinical Important Difference of the Multiple Sclerosis Questionnaire for Physiotherapists

Start date: April 2011
Phase: N/A
Study type: Observational

The aim of this survey is the evaluation of the responsiveness and the estimation of the MCID of the German and French Multiple Sclerosis Questionnaire for Physiotherapists, a self-rating Patient Reported Outcome questionnaire. This multicenter project uses a combined anchor and distribution based approach with multiple anchors to provide a range of MCID estimates or a single MCID for the reliable and valid Items, Activity and Participation group and the Total Score of the MSQPT, which should to be used as guidelines in daily practice.

NCT ID: NCT02340754 Completed - Multiple Sclerosis Clinical Trials

Mindfulness-based Stress Reduction for Multiple Sclerosis

Start date: May 2015
Phase: N/A
Study type: Interventional

The primary purpose of this study is to assess the feasibility of mindfulness-based stress reduction (MBSR) for adults with any type of multiple sclerosis. The secondary objectives are to: 1) Explore the ability of MBSR to improve perceived stress and quality of life compared to an education control group; and 2) Explore the durability of the effects of MBSR over one year.

NCT ID: NCT02339688 Completed - Multiple Sclerosis Clinical Trials

Psychometric Properties Mobility Measures MS

MCS-III-MOB
Start date: October 2014
Phase: N/A
Study type: Interventional

Current study will investigate the quality (psychometric properties) and clinical utility of several mobility measures, according to disability level. Therefore, several aspects will be inquired: - Was there an effect of rehabilitation - Is the measure able to detect change over time? And thus the change exceed measurement error and is it clinically important (responsiveness) - Does the measure assess what it claims to measure (validity) - Is the measure able to differentiate all performances of the patients, inclusively the very good and very bad performances (floor and ceiling effects) - Does the measure gives similar results under consistent test conditions on another testing day (reliability) Worldwide, theoretical approaches to physical therapy and rehabilitation in Multiple Sclerosis often appear significantly different. Since the present research protocol will be performed at different centers across European countries (and US sites), this multi-center study can additionally be applied for mapping the volume and content of rehabilitation, as well as the differential impact of diverse rehabilitation approaches and training volume on mobility, for several disability levels. Some health-economic analyses will be performed to examine what the approximate cost of rehabilitation compared to effects is and what drivers of costs are (setting, equipment, staff).

NCT ID: NCT02339675 Completed - Multiple Sclerosis Clinical Trials

Psychometric Properties Upper Limb Function Measures Multiple Sclerosis

MCS-III-UL
Start date: October 2014
Phase: N/A
Study type: Interventional

Current study will investigate de quality (psychometric properties) and clinical utility of several measures of upper limb function, according to disability level. Therefore, several aspects will be inquired: - Was there an effect of rehabilitation - Is the measure able to detect change over time? And thus the change exceed measurement error and is it clinically important (responsiveness) - Does the measure assess what it claims to measure (validity) - Is the measure able to differentiate all performances of the patients, inclusively the very good and very bad performances (floor and ceiling effects) - Does the measure gives similar results under consistent test conditions on another testing day (reliability) Worldwide, theoretical approaches to physical therapy and rehabilitation in Multiple Sclerosis often appear significantly different. Since the present research protocol will be performed at different centers across European countries (and US sites), this multi-center study can additionally be applied for mapping the volume and content of rehabilitation, as well as the differential impact of diverse rehabilitation approaches and training volume on mobility, for several disability levels. Some health-economic analyses will be performed to examine what the approximate cost of rehabilitation compared to effects is and what drivers of costs are (setting, equipment, staff).

NCT ID: NCT02335892 Completed - Clinical trials for Relapsing Remitting Multiple Sclerosis

PROFILE - Evaluation of QoL and PRO Outcomes in Patients Taking Fingolimod

PROFILE
Start date: November 11, 2014
Phase:
Study type: Observational

Multi centre, prospective, non interventional study in 200-240 UK relapsing remitting multiple sclerosis patients. Patients will complete questionnaires at baseline, 3, 6 and 12 months.