Skip to content

Effect of Carnitine Supplementation and Resistance Training on Skeletal Muscle Function

Effect of Carnitine Supplementation and Resistance Training on Skeletal Muscle Function in Aging

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03907592
Enrollment
60
Registered
2019-04-09
Start date
2017-09-01
Completion date
2018-07-07
Last updated
2019-04-10

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

Conditions

Sarcopenia

Keywords

L-Carnitine, Resistance training, Magnetic resonance imaging, Muscle function, Aging, Leucine

Brief summary

The primary aim of the current research project is to explore whether nutritional supplementation and resistance training might be combined to produce synergistic effects in the prevention of muscle loss during aging. A secondary aim of this project is to investigate the effects of carnitine with leucine supplementation, in comparison to carnitine supplementation alone, on muscle strength and body composition. The hypothesis is that resistance training combined with nutritional supplementation have a more beneficial effect than resistance training alone in the prevention of muscle loss during aging. Leucine stimulates carnitine transport into the muscle cells, which improve mitochondrial capacity. Modification in energetic of skeletal muscle affects the body composition and muscle performance.

Detailed description

The study will be included volunteers - women between 60 - 72 years old (n=60). The patients are randomly assigned to two experimental groups (n=20) and control group (n=20). During the 24-weeks intervention period, Group A undergoes training procedure supplemented with the carnitine and leucine, whilst group B undergoes training procedure supplemented with leucine. At the same time control group go through only training procedure. Measurements are performed before, at the mid-point, and at the end of the intervention period. Approximately 1 week prior to the experimental trial day, participants perform a familiarization session during which one-repetition maximum (1RM) strength testing is also performed to determine the experimental exercise load. Resistance exercise training is performed twice weekly on non-consecutive days (Monday+Thursday, or Tuesday+Friday) for 24-weeks under direct supervision by a research assistant. Prior to a training session subjects are required to perform warm - up on the treadmill (walk) and static stretching, after each session - cool down on the cycle ergometer and static stretching. Resistance exercise for each session consisted of 6 exercises: horizontal seated leg press, seated chest press, leg extension, shoulder press, lat pull-down seated row, seated cable row First two weeks of training consist of 3 sets of 10-12 repetitions and are keeping exercises at 65% of 1 repetition maximum (1RM). After this period training consists of 3 sets of 6-8 repetitions and is progressing to 80% of 1RM. The 1RM is re-evaluated every 2 weeks, and the training load is adjusted accordingly. The exercise program follows the recommended guidelines for older adults by the American College of Sports Medicine and the National Strength and Conditioning Association.

Interventions

DIETARY_SUPPLEMENTL-carnitine supplementation

Supplementation of 1000 mg L-carnitine-L-tartrate in combination with 3000 mg L-leucine per day throughout the study period.

DIETARY_SUPPLEMENTLeucine supplementation

Supplementation of 4000 mg L-leucine per day throughout the study period.

PROCEDUREResistance training

Resistance training at the gym, twice a week for 24 weeks (48 training units in total).

Sponsors

Medical University of Gdansk
CollaboratorOTHER
National Science Centre, Poland
CollaboratorOTHER_GOV
Gdansk University of Physical Education and Sport
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
60 Years to 72 Years
Healthy volunteers
Yes

Inclusion criteria

* aged-matched, no chronic disease, doctor's note about the lack of restrictions to perform resistance exercises

Exclusion criteria

* diabetes, liver, heart and renal diseases, gastric problems, as well as using the vitamin supplements

Design outcomes

Primary

MeasureTime frameDescription
Volumetric changes in knee extensor muscleValues at baseline will be compared to values recorded at 12 and at 24 weeks after supplementation and training procedure.Volumetric examination of cross section area (CSA) of knee extensor muscles determined by a 1.5 T MRI scanner.

Secondary

MeasureTime frameDescription
Changes in the strength of muscle knee extensorValues at baseline will be compared to values recorded at 12 and at 24 weeks after supplementation and training procedure.Maximal isometric knee extensor peak torques determined by the dynamometer (Biodex System 4 Pro).
Changes in Lean Body MassValues at baseline will be compared to values recorded at 12 and at 24 weeks after supplementation and training procedure.Lean Body Mass measured by dual-energy X-ray absorptiometry (DXA).

Countries

Poland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026