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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05108181
Other study ID # BC-10253
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 9, 2021
Est. completion date December 8, 2023

Study information

Verified date April 2024
Source University Ghent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall aim of this project is to investigate if the responsiveness to chronic resistance training is dependent on the muscle typology. In a second aim we will investigate the most optimal training frequency for slow-twitchers and fast-twitchers. For the latter we hypothesize that slow-twitchers might cope better with higher frequencies and higher volumes compared to fast-twitchers. Male and female adult participants (18-45y) will be recruited. The subjects' muscle typology will be non-invasively estimated in the leg muscles by measurement of muscle carnosine using H-MRS. In total 21 subjects (11 slow and 10 fast subjects) will participate. Subjects will be assigned to a whole-body resistance training exercise protocol of 9 weeks in wich arm A and leg A will train 3 times per week and arm B and leg B will train 2 times per week. Before and following the training period, subjects will be subjected to different measurements (fitness level, muscle volume, strength tests, blood sampling, muscle biopsies).


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 8, 2023
Est. primary completion date December 8, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Fast or slow muscle typology - 18 - 45 years old - no strength training experience Exclusion Criteria: - Vegan/vegeterian diet - Supplement intake - chronic diseases - Hypertension, - Smoking - Medication use - Coagulation disorder, infectious diseases

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Muscle typology + exercise training
Exercise training: Participants perform 9 weeks of strength training at 60% of their 1RM.
Muscle typology + training frequency
Training frequency: leg A and arm A of the participants train 3 times per week, leg B and arm B train 2 times per week.

Locations

Country Name City State
Belgium Department of Movement and Sports Sciences, Ghent University Gent Oost-Vlaanderen

Sponsors (1)

Lead Sponsor Collaborator
University Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from baseline muscle volume at 9 weeks Muscle volume of the legs and the upper arms - MRI Pre and post the 9 weeks training period
Primary Change from baseline dynamic muscle strength at 3 weeks Upper legs and upper arms - strength training devices Pre, mid and post 9 weeks training period
Primary Change from baseline dynamic muscle strength at 6 weeks Upper legs and upper arms - strength training devices Pre, mid and post 9 weeks training period
Primary Change from baseline dynamic muscle strength at 9 weeks Upper legs and upper arms - strength training devices Pre, mid and post 9 weeks training period
Primary Change from baseline isometric muscle strength at 9 weeks Upper legs and upper arms - Biodex Pre and post 9 weeks training period
Primary Change in muscle fiber type specific hypertrophy at 9 weeks Legs - Biopsy (vastus lateralis) Pre and post 9 weeks training period
Secondary Change of baseline antropometry at 9 weeks Height, weight, skinfolds Pre and post 9 weeks training period
Secondary Change of baseline skeletal muscle protein content at 9 weeks Histochemistry and protein content of markers of relevance for skeletal muscle function Pre and post 9 weeks training period
Secondary Change of baseline histochemistry at 9 weeks Histochemistry of markers of relevance for skeletal muscle function Pre and post 9 weeks training period
Secondary Change from basline fatigue feeling over 9 weeks training period Number of repetitions during every training, questionnaire (VAS-scale) before every training, RPE after every training Assessed every training during the 9 weeks training period
Secondary Change from baseline fasting insulin, glucose, cholesterol and triglycerides at 9 weeks Fasted blood samples Pre and post 9 weeks training period
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