Aerobic Exercise Clinical Trial
Official title:
The Effect of Different Order of Concurrent Training Consisting Aerobic and Resistance Exercise on Improving Visceral Adipose Tissue and Insulin Resistance for Community Residents With Obesity.
NCT number | NCT05580263 |
Other study ID # | 110-551 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 31, 2022 |
Est. completion date | June 30, 2023 |
Verified date | February 2024 |
Source | National Tainan Junior College of Nursing |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Purposes: The purpose of one-year project is to compare the effect of different intrasession exercise order of AE and RE during concurrent training on reducing VAT and improving insulin resistance for inactive middle-age community residents with obesity. Methods: Purposive sampling will be used to enroll community residents aged 40-64 years with inactive habit and body fat percentage ≧ 25% for male and ≧ 30% for female in southern Taiwan. Eligible participants will be stratified by sex and age (40-55years and 56-64 years) then block randomly divided into training group of AE preceding RE, RE preceding AE or a control group. The exercise training program will under supervision lasting 16 weeks with 3 times per week. The concurrent training prescription consist of AE 30 minutes and RE 15 minutes per session. A 5-minute interval between two exercise modalities. All participants will be evaluated outcomes for two time points including baseline (T0) and after 16-week intervention (T1). The primary outcomes are VAT and insulin resistance. A two-way ANOVA with repeated measures will be performed to compare changes of outcome variables over the intervention period. Relevance to clinical practice: The results of this project can assist health professionals to know how to properly prescribe concurrent training of AE and RE to achieve the greatest effects on VATreduction and insulin resistance improvement for middle-age residents with obesity.
Status | Completed |
Enrollment | 92 |
Est. completion date | June 30, 2023 |
Est. primary completion date | June 30, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 40 Years to 64 Years |
Eligibility | Inclusion Criteria: - 40 to 64 years old. - body fat percentage ? 25% for male and ? 30% for female. - with inactive habit (= 3 days of physical activity per week and = 30 min per session). - can communicate in Mandarin or Taiwanese. Exclusion Criteria: - with recent unstable conditions in which had potential risk on exercise including stroke, cardiovascular and respiratory diseases, handicap, pregnancy. - with any contraindications to body composition analyzer measurement including body embed pacemakers and artificial metal joints, amputated hands or feet. - cannot corporate with either examination or intervention. - use psychotropic or appetite-regulating medicine. - under oral hopoglycemic agent or insulin treatment. |
Country | Name | City | State |
---|---|---|---|
Taiwan | Natioal Tainan Junior College of Nursing | Tainan |
Lead Sponsor | Collaborator |
---|---|
National Tainan Junior College of Nursing |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | visceral adipose tissue | Participants will measure visceral adipose tissue measure at baseline by body composition analyzer. | at baseline | |
Primary | visceral adipose tissue | Participants will measure visceral adipose tissue measure after 16-week intervention by body composition analyzer. | 16-week after intervention | |
Primary | Insulin | Participants will collect insulin at baseline by blood samples | at baseline | |
Primary | Insulin | Participants will collect insulin after 16-week intervention by blood samples | 16-week after intervention | |
Primary | Fasting glucose | Participants will collect fasting glucose at baseline by blood samples | at baseline | |
Primary | Fasting glucose | Participants will collect fasting glucose after 16-week intervention by blood samples | 16-week after intervention | |
Secondary | waist circumference | Participants will measure waist circumference at baseline by tape measurement | at baseline | |
Secondary | waist circumference | Participants will measure waist circumference after 16-week intervention by tape measurement | 16-week after intervention | |
Secondary | hip circumference | Participants will measure hip circumference at baseline by tape measurement | at baseline | |
Secondary | hip circumference | Participants will measure hip circumference after 16-week intervention by tape measurement | 16-week after intervention | |
Secondary | weight | Participants will measure weight at baseline by body composition analyzer | at baseline | |
Secondary | weight | Participants will measure weight after 16-week intervention by body composition analyzer | 16-week after intervention | |
Secondary | body fat percentage | Participants will measure body fat percentage at baseline by body composition analyzer | at baseline | |
Secondary | body fat percentage | Participants will measure body fat percentage after 16-week intervention by body composition analyzer | 16-week after intervention |
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