Clinical Trials Directory

Trials / Completed

CompletedNCT05120011

Carnitine Supplementation and Bone Mineral Density

Effect of Carnitine Supplementation and Resistance Training on Bone Mineral Density

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
36 (actual)
Sponsor
Poznan University of Physical Education · Academic / Other
Sex
Female
Age
60 Years – 75 Years
Healthy volunteers
Accepted

Summary

The primary aim of the current research project is to explore whether carnitine supplementation and resistance training may prevent decrements in bone mineral density of aged women. A secondary aim of this project is to investigate the effect of supplementation on body composition and blood markers.

Detailed description

The study includes postmenopausal women. The subjects participate in resistance training (twice a week) 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. During the 24-weeks training programme participants are supplemented by carnitine with leucine, or leucine alone (placebo).

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTL-carnitineL-carnitine-L-tartrate
DIETARY_SUPPLEMENTL-leucineL-leucine

Timeline

Start date
2017-09-01
Primary completion
2018-07-07
Completion
2018-07-07
First posted
2021-11-15
Last updated
2022-08-16

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT05120011. Inclusion in this directory is not an endorsement.