None listed
Conditions
Interventions
Behavioral, Dietary Supplement : Intervention 1. Control Group:
Participants maintain their usual daily life for 12 weeks, and no separate exercise or supplement intake intervention is provided.
Inte
Sponsors
Kangwon National University
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: Min 65 years ~ Max 78 years (1) Individuals aged 65 years or older who were able to participate in regular resistance exercise; (2) Individuals who voluntarily agreed to participate in the study; (3) A total of 100 elderly people without insulin resistance (HOMA-IR = 2.5) were recruited.
Exclusion criteria
Exclusion criteria: (1) Individuals diagnosed with a musculoskeletal disorder in the past 6 months that prevents them from participating in walking or exercise programs; (2) Individuals with severe cardiovascular disease that precludes participation in resistance exercise programs; (3) Individuals unable to perform daily activities independently due to depression, anxiety, or insomnia; (4) Individuals currently taking any medication to lower blood glucose levels; (5) Individuals who are currently on a diet or planning to start a diet, or those already participating in two or more structured exercise sessions per week; (6) Individuals deemed unsuitable for participation in this clinical trial due to other medical conditions that may affect the outcomes, as determined by the attending physician or research staff. However, individuals taking antihypertensive or lipid-lowering medications will be allowed to participate if their medication regimen remains stable throughout the study period.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body compositon(Height, Muscle mass, Fat mass, Fat percent);Myokine;Insulin;Inflammation | — |
Secondary
| Measure | Time frame |
|---|---|
| physical fitness | — |
Countries
Korea, Republic of
Contacts
Public ContactDeokhwa Jeong
Kangwon National University
Outcome results
None listed