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Effects of recreational Volleyball program in Obese adolescents

Effects of a 12-week recreational Volleyball program in Obese adolescents: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7rrrvjw
Enrollment
Unknown
Registered
2025-04-02
Start date
2025-04-01
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

Body Weight

Interventions

A randomized controlled trial will be conducted with 40 adolescents (12-17 years) over 12 weeks. Initially, a randomization will be carried out, where each individual selected according to the inclusi
I03.450.642.845.932

Sponsors

Instituto de Educação Física e Esportes
Lead Sponsor
Universidade Federal do Ceará
Collaborator

Eligibility

Age
12 Years to 17 Years

Inclusion criteria

Inclusion criteria: Be between 12 and 17 years old; both genders; display body mass index > 2 standard deviations above the specific for the age and se according to the World Health Organization reference medians; be in the final stages of the pubertal maturation

Exclusion criteria

Exclusion criteria: Have medical conditions that contraindicate participation in physical activities; the use of medication that influences the results observed; participation in structured exercise, nutrition or weight loss programs weight in the 6 months prior to the initial screening

Design outcomes

Primary

MeasureTime frame
It is expected that the body mass of the individuals undergoing the intervention will decrease after this period compared to that presented at the previous time.

Secondary

MeasureTime frame
It is expected that the physical fitness of the individuals undergoing the intervention will improve after this period compared to that presented at the previous time.

Countries

Brazil

Contacts

Public ContactAlexandre Medeiros

Universidade Federal do Ceará

alexandremedeiros@ufc.br+55 (85) 33669217

Outcome results

None listed

Source: REBEC (via WHO ICTRP)