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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03222596 |
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Date of registration:
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16/07/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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The Impact of Exercise Training on Living Quality in Multiple Sclerosis Individuals
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Scientific title:
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The Impact of 4-weeks Mild Exercise Training on Living Quality in Ambulatory and Non-ambulatory Multiple Sclerosis Individuals (EDSS From 0-8) in Motivational and Social Supporting Environment: a Randomized Controlled Trial |
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Date of first enrolment:
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July 14, 2017 |
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Target sample size:
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40 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03222596 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Croatia
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Contacts
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Name:
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Tanja Grubic Kezele, PhD, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Biomedicine investigations |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Individuals with multiple sclerosis (EDSS 0-8)
- Ambulatory and non-ambulatory (in wheelchairs)
Exclusion Criteria:
- Individuals with contraindications for exercising
- Individuals with multiple sclerosis with EDSS over 8
Age minimum:
21 Years
Age maximum:
70 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Physical Activity
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Pain
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Disabilities Psychological
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Fatigue
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Mental Impairment
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Motivation
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Physical Disability
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Energy Supply; Deficiency
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Mental Status Change
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Multiple Sclerosis
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Quality of Life
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Disability Physical
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Intervention(s)
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Behavioral: Exercise training
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Primary Outcome(s)
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Change of grip strength.
[Time Frame: baseline, after 4 weeks]
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Change of fatigue intensity
[Time Frame: baseline, after 4 weeks]
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Change of physical abilities and limitations.
[Time Frame: baseline, after 4 weeks]
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Change of pain intensity
[Time Frame: baseline, after 4 weeks]
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Change of mental abilities and limitations.
[Time Frame: baseline]
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Change of quality of life.
[Time Frame: baseline, after 4 weeks.]
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Motivation.
[Time Frame: baseline, after 4 weeks]
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Secondary ID(s)
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602-01/17-01-147
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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