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Effect of exercise on adolescent health risk factors

Combined Physical Exercise and Cardiometabolic Risk Factors in Adolescents

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7js6r9
Enrollment
Unknown
Registered
2018-01-31
Start date
2018-04-02
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Interventions

Experimental Design A randomized and controlled clinical trial lasting 12 weeks will be adopted for the present investigation. To do so, 80 participants will be subdivided into four distinct groups, n
group 2 - combined intervention in overweight (n = 20)
group 3 - eutrophic control (n = 20)
group 4 - overweight control (n = 20). All groups will be accompanied by a nutritionist. The data collection will be carried out in the Laboratory of Biodynamics of the Human Movement, of the Health S
WESTON , WISLØFF, COOMBES, 2013, WISLØFF et al., 2007, WISLØFF, COOMBES, ROGNMO, 2015). Thus, each session will begin with five minutes of warm-up, with intensity of 50% of HRmax on the treadmill. The
Behavioural
Other
G11.427.410.698.277
E02.760.169.063.500.387.875

Sponsors

Universidade Estadual do Norte do Paraná
Lead Sponsor
Universidade Estadual do Norte do Paraná
Collaborator

Eligibility

Age
15 Years to 19 Years

Inclusion criteria

Inclusion criteria: Be between 15 and 19 years old; not have recognized cardiovascular disease; no diagnosis of diabetes and hypertension; not been participating in a physical activity / exercise program for at least three months; do not present limiting conditions for the practice of physical exercises

Exclusion criteria

Exclusion criteria: Report stage of sexual maturation below IV, present body mass index greater than 40; do not meet pre-participation recommendations on physical tests and weekly sessions.

Design outcomes

Primary

MeasureTime frame
Expected outcome 1: reduction of fat percentage (~5%) after 12 weeks of intervention, estimated using the skinfold method;Expected outcome 2: reduction of percentage of glycated hemoglobin (~2%) after 12 weeks of intervention, analyzed by means of high efficiency liquid chromatography;Expected outcome 3: decrease in resting blood pressure values (~10%) after 12 weeks of intervention, measured by a digital device with dimensions appropriate for the circumference of the arm

Secondary

MeasureTime frame
Expected outcome 1: improvement in cardiorespiratory fitness (~50%) after 12 weeks of intervention, analyzed by means of the 20-meter back-and-forth test.;Expected outcome 2: increased strength and muscular endurance (30-50%) after 12 weeks of intervention, verified through arm flexion, horizontal and abdominal bounce tests in one minute.

Countries

Brazil

Contacts

Public ContactWaynne Faria

Universidade Estadual do Norte do Paraná

fariawf@outlook.com+55 (043) 3525-0498

Outcome results

None listed

Source: REBEC (via WHO ICTRP)