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Effects of Combined Concurrent Training with Cricket Peptide Supplementation on Cardiometabolic and Functional Fitness Parameters in Older Adults

Phase 2
Completed
Conditions
Older adults
aging
combined exercise
physical fitness
protein supplementation
quality of life
Registration Number
TCTR20230208010
Lead Sponsor
Graduate School, Kasetsart University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
44
Inclusion Criteria

1. Males and females aged 55 and over
2. Body mass index between 18.5-27.5 kg/m2
3.Systolic blood pressure equal to or greater than 130 mmHg and/or diastolic blood pressure equal to or greater than 85 mmHg
4. Availability to attend the exercise program three times a week

Exclusion Criteria

1. The allergic reaction with crustaceans
2. Current smoking
3. Unstable and/or uncontrolled cardiovascular diseases
4. Musculoskeletal problems to physical exercise
5. Severe visual impairment
6. Kidneys or livers disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Body composition before and after 12 weeks of intervention Dual-energy X-ray,Physical function before and after 12 weeks of intervention Senior fitness test,Muscle strength before and after 12 weeks of intervention 1RM of bench press and leg press,Insulin-like growth factor-1 before and after 12 weeks of intervention IRMA kits ,Fasting blood glucose before and after 12 weeks of intervention automated analyzer ,Plasma insulin concentration before and after 12 weeks of intervention commercial radioimmunoassay kits ,Lipid profiles before and after 12 weeks of intervention automated colorimetric assay ,Serum hs-CRP concentration before and after 12 weeks of intervention high-sensitivity immunoturbidimetric assay ,Blood pressure before and after 12 weeks of intervention automated sphygmomanometer,Arterial stiffness before and after 12 weeks of intervention pulse wave velocity,Heart rate variability before and after 12 weeks of intervention eMotion Faros
Secondary Outcome Measures
NameTimeMethod
Quality of life before and after 12 weeks of intervention World Health Organization Quality of Life Brief Version Thai
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