University of Saskatchewan
Saskatoon, SK - Saskatchewan, S7N 5B2, Canada
Location status: Recruiting
NCT Number: NCT07625202
GLP-1 receptor agonists are effective for weight loss, but significant muscle mass is lost as a proportion of this weight loss. This study combines resistance-training and creatine supplementation to try to prevent this loss of muscle mass.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Saskatoon, SK - Saskatchewan, S7N 5B2, Canada
Location status: Recruiting
GLP-1 receptor agonists are highly effective for weight loss and increasing in popularity for those trying to lose weight. One concern with these medications is the potential for loss of lean tissue mass during rapid weight loss. This may affect strength and functional performance in people taking these medications. Resistance-training helps to offset loss of muscle mass during weight loss. Supplementation with creatine monohydrate is also effective for improving muscle mass and strength. The purpose of this pilot study is to determine the effectiveness of creatine supplementation during a resistance training program in people who are starting GLP-receptor agonist medication for preventing loss of lean tissue mass and functional performance. The investigators will randomize 40 people who are starting GLP-1 agonists to receive either 10g per day creatine or placebo during a resistance-training program (i.e., resistance-training three days per week for 12 weeks). It is hypothesized that participants on the creatine supplement will have superior maintenance of lean tissue mass and function performance compared to participants taking placebo.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
creatine supplementation
Placebo
Time frame: 12 weeks
change in number of times sitting and standing in 30 seconds
Time frame: 12 weeks
change in walking speed over 10 meters
Time frame: 12 weeks
change in time to stand up, walk 3m, turn, around, walk 3 m and sit down
Time frame: 12 weeks
Change in lean tissue mass as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in fat mass as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in bone mineral density as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in bone mineral density as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in bone mineral density as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in bone mineral density as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in hip section modulus as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in muscle thickness measured by ultrasound
Time frame: 12 weeks
Change in muscle thickness measured by ultrasound
Time frame: 12 weeks
change in upper body strength measured by predicted one repetition maximum
Time frame: 12 weeks
Change in lower body strength measured by predicted one repetition maximum
Time frame: 12 weeks
Change in hip buckling ratio as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in hip cross-sectional area as determined by dual energy x-ray absorptiometry
Time frame: 12 weeks
Change in hip cortical thickness as determined by dual energy x-ray absorptiometry
Contact information is provided by the study sponsor or research team.
University of Saskatchewan
Other
A Pilot Study on Creatine Supplementation During Resistance-training for Prevention of Lean Tissue Mass Loss During GLP-1 Receptor Agonist Therapy
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06329622
Atrophy, Chronic Disease
Shanghai, China
View Trial DetailsNCT07715721
Atrophy, Mental Disorders
Tainan, Taiwan
View Trial DetailsNCT07724587
Atrophy, Muscular Atrophy
Ningbo, China
View Trial DetailsNCT07500376
Atrophy, Bronchial Neoplasms
Samsun, Turkey (Türkiye)
View Trial Details