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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03636854
Other study ID # ConEcc
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 15, 2018
Est. completion date May 28, 2019

Study information

Verified date July 2020
Source Dokuz Eylul University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study is to compare the effects of concentric and eccentric exercises on muscle strength, muscle thickness and balance in healthy Individuals. Participants will randomly be divided into 2 groups: Concentric exercise (CE) group, eccentric exercise (EE) group. Concentric exercise group will be doing 2 concentric exercises and eccentric exercise group will be doing 2 eccentric exercise for 8 weeks. The evaluations will be repeated after 8 weeks of training to reveal the effects of concentric and eccentric exercises.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date May 28, 2019
Est. primary completion date April 15, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 25 Years
Eligibility Inclusion Criteria:

- Age between 18-25

- Healthy individuals

- Able to read, write and understand Turkish

- Willing and able to attend study

Exclusion Criteria:

- Any neurological, musculoskeletal or vascular disease in any of the lower extremity

- Having lower extremity musculoskeletal pain

- Previous history of surgery in any of the lower extremity

- Mental and cognitive disorders that would seriously affect cooperation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Concentric exercises
Resistance concentric straight leg raise and knee extension will be done.
Eccentric exercises
Resistance eccentric straight leg raise and knee extension will be done.

Locations

Country Name City State
Turkey Dokuz Eylul University Izmir

Sponsors (1)

Lead Sponsor Collaborator
Dokuz Eylul University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in muscle thickness Change in muscle thickness will be measured by using Ultrasound Before training and after 8 weeks of training
Secondary Change in muscle strength Change in muscle strength will be assessed by using hand-held dynamometer. Before training and after 8 weeks of training
Secondary Change in balance Change in balance will be measured by using Biodex Balance System. Before training and after 8 weeks of training
Secondary Change in function Change in function will be measured by using single leg hop test Before training and after 8 weeks of training
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