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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04853654
Other study ID # ipekkirmaci
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 15, 2018
Est. completion date June 15, 2020

Study information

Verified date December 2021
Source Sanko University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Selective exercise programs specific to muscle groups, with the workload to be done in line with the muscle's own structure, can enable more strength to be released with less fatigue in MS, and this increase in strength can increase balance and functional activities. to determine the effects of type training (selective exercise training), eccentric and concentric training on function, balance, fatigue and muscle architecture.


Description:

Recovery and enhancement of muscle function in MS is one of the main goals in physiotherapy and rehabilitation. In literature studies, it is stated that eccentric and concentric exercises are effective exercise approaches in increasing strength and reducing fatigue. However, the best exercise method is not yet clear in terms of providing better performance adaptation with less fatigue. Considering the architectural features of the lower extremity muscles, it is aimed to increase the angle of pennation with programs that include concentric strengthening of the quadriceps, gastro-soleus and gastrocnemius muscles, which are suitable muscle groups to produce large forces by design. With programs that include eccentric strengthening of the hamstring and tibialis anterior muscles that function in a wide range of motion and have high excursion ability, it is aimed to increase fiber length.


Recruitment information / eligibility

Status Completed
Enrollment 33
Est. completion date June 15, 2020
Est. primary completion date April 15, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: - Between the ages of 18-50, - With an Extended Disability Status Scale (EDSS) score of 4 or less, - No regular exercise habit - Able to walk on the treadmill, - No pregnancy, - Not receiving corticosteroid treatment in the last month, - Fampridine etc. in the last 1 month. not taking medication, - Patients who have not received Botox treatment in the last 6 months Exclusion Criteria: patients who do not agree to volunteer

Study Design


Related Conditions & MeSH terms


Intervention

Other:
exercise
exercise training for 8 weeks

Locations

Country Name City State
Turkey Zekiye Ipek Katirci Kirmaci Gaziantep

Sponsors (1)

Lead Sponsor Collaborator
Sanko University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary muscle architecture parameter 1 The pennation angle were evaluated with Ultrasound Change from Baseline at 8th weeks and 12th weeks
Primary muscle architecture parameter 2 The fiber length were evaluated with Ultrasound Change from Baseline at 8th weeks and 12th weeks
Primary muscle architecture parameter 3 The muscle thickness were evaluated with Ultrasound Change from Baseline at 8th weeks and 12th weeks
Primary Muscle strength low extremity muscles were evaluated with hand dynamometer Change from Baseline at 8th weeks and 12th weeks
Secondary walking fatigue Walking Fatigue Index Change from Baseline at 8th weeks and 12th weeks
Secondary perceived fatigue Fatigue Severity Scale Change from Baseline at 8th weeks and 12th weeks
Secondary physical fatigue Modified Borg Scale before and after 6-minute walking test Change from Baseline at 8th weeks and 12th weeks
Secondary static balance Single standing tests Change from Baseline at 8th weeks and 12th weeks
Secondary dynamic balance 4 square step tests Change from Baseline at 8th weeks and 12th weeks
Secondary Functional activities 1 timed-up go test Change from Baseline at 8th weeks and 12th weeks
Secondary Functional activities 2 2-minute walk test Change from Baseline at 8th weeks and 12th weeks
Secondary Functional activities 3 25-feet walk test Change from Baseline at 8th weeks and 12th weeks
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