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N/A N=50 Randomized Treatment

Isokinetic Exercises in Patients With Multiple Sclerosis

Multiple Sclerosis

Enrolled (actual)
50
Serious AEs
Results posted
Jul 2019
Primary outcome: Primary: Isokinetic Muscle Strength Test of the More and Less Affected Knees — 110.48; 141.05; 123.02; 127.83 Newton/meter

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
exercises (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Aksaray University Training and Research Hospital
Primary completion
Jul 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Isokinetic Muscle Strength Test of the More and Less Affected Knees
110.48; 141.05; 123.02; 127.83; 69.25; 85.87
PRIMARY
Joint Position Sense of the More and Less Affected Knees
5.56; 4.39; 5.70; 5.03; 4.94; 4.38
PRIMARY
Tampa Scale of Kinesiophobia
42.42; 40.57; 40.33; 40.33
PRIMARY
Multiple Sclerosis Quality of Life-54 Total Score, Physical and Emotional Composite Scores, and Pain Subscale Score
52.20; 57.00; 61.38; 59.39; 50.79; 54.69
PRIMARY
Visual Analog Scale
40.78; 36.68; 41.66; 42.14

Summary

The investigators evaluated the effects of isokinetic muscle strengthening exercises of the quadriceps and hamstring on muscle strength, joint position sense, pain, kinesiophobia and quality of life in patients with multiple sclerosis.

Eligibility Criteria

Inclusion Criteria

  • definite relapsing remitting MS and secondary progressive MS diagnosis
  • mild and moderate MS determined by Kurtzke Expanded Disability Status Scale (EDSS) scores below 6.5
  • a disease duration of more than one year.

Exclusion Criteria

  • having an acute exacerbation within the last three months
  • intravenous pulse steroid therapy in the last four weeks
  • grade 3-4 spasticity according to the Modified Ashworth Scale
  • severe vision impairment
  • severe fatigue and depression
  • past knee surgery
  • other neurologic diseases
  • systemic diseases
  • pregnancy
  • having received an exercise program within the last four weeks.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03779724). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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