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Exercise Training in Healthy Young Men

The Impact of Timed Protein Supplementation to Maximize the Skeletal Muscle Adaptive Response to Resistance Type Exercise Training in Healthy Young Men

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02222415
Enrollment
44
Registered
2014-08-21
Start date
2011-10-31
Completion date
2012-02-29
Last updated
2014-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gaining Skeletal Muscle Mass and Strength

Keywords

Muscle mass, Strength, Cross-sectional area, Protein

Brief summary

Resistance type exercise training has been shown to be a potent stimulus to increase skeletal muscle mass and strength in healthy men. Furthermore, timed protein intake is also known to affect the muscle adaptive response following exercise. Whether timed protein intake could augment the increase in muscle fiber size and/or satellite cell content following long-term exercise intervention remains to be established. We hypothesize that protein supplementation before sleep, on both training and non-training days, during a 12 week resistance training program further increases type II muscle fibre cross sectional area when compared to the placebo group.

Interventions

DIETARY_SUPPLEMENTExercise + Protein drink

Sponsors

Maastricht University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Male * Healthy * Age between 18 and 30 years * BMI between 18.5 and 30 kg/m2 * Recreationally active, performing sports on a non-competitive basis between 2 and 5 hours p/wk * Participants willing and able to give written informed consent and to understand, to participate and to comply with the biomedical research project requirements

Exclusion criteria

* HbA1C level above 6.5% * Fasted blood glucose level above 7 mmol/L * Serum creatinine level beneath 60 or above 120 µmol/L * Participants with a recent history or current state of COPD * Participants with a recent history or current state of rheumatoid arthritis * Participants with a recent history or current state of musculoskeletal/orthopedic disorders * Participants with a recent history or current state of renal disorder * Participants with a recent history or current state of cognitive impairment * Participants with orthopedic metal implants in the spine and/or upper/lower extremities * Participants with lactose intolerance and/or dairy protein allergy * Participants who are enrolled in an interventional biomedical research project or have received an investigational new drug or product with the last 30 days prior to screening. * Participants on medication, including anticoagulants

Design outcomes

Primary

MeasureTime frameDescription
Skeletal muscle fiber size12 weeksSkeletal muscle fiber size will be assessed by muscle biopsy sampling before, during and after the 12 wks intervention period. Muscle fiber size will be expressed in µm2

Secondary

MeasureTime frameDescription
Quadriceps cross-sectional area12 weeksQuadriceps cross-sectional area will be assessed by CT-scan before and after the 12 wks intervention period. Quadriceps cross-sectional area will be expressed in cm2
Whole body en regional body composition12 weeksBody composition (whole-body as well as regional) well be determined by DXA-scan performed before and after the 12 wks intervention period. Results will be expressed in kilograms
1RM strength12 weeksMaximum muscle strength will be assessed before, during and after 12 wks of exercise training by means of a 1 rep max test and will be expressed in kilograms.

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026