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This study aims to evaluate the effects of different basketball training programs on adolescents with obesity. The objective is to assess how these programs influence body weight, physical fitness, motivation to exercise, and basketball skills.
Three types of programs are being compared:
Participants are adolescents aged 15 to 17 years with moderate obesity who will engage in one of the programs for seven weeks, with one training session per week.
Body weight, physical fitness, motivation, and basketball skills will be measured before and after the intervention to determine which approach is most effective.
The study aims to identify engaging and effective methods for promoting physical activity, health, and basketball skill development in adolescents with obesity.
Full description
This randomized controlled trial (RCT) includes three parallel intervention arms designed to evaluate the effects of different basketball teaching programs on adolescents with obesity. The intervention spans seven consecutive weeks and consists of one structured basketball session per week, each lasting 60 minutes and delivered during regular physical education (PE) classes.
A total of 55 adolescents (33 females and 22 males), aged 15 to 17 years and classified as having moderate obesity (BMI: 30-34.9 kg/m²), were recruited from a secondary school in the Sidi Bouzid region of Tunisia. Participants were randomly assigned using a computer-generated sequence to one of the following groups:
Pre- (T0) and post-intervention (T1) assessments included: (i) anthropometric measurements (BMI), (ii) physical fitness tests, (iii) evaluations of technical basketball performance (passing, dribbling, shooting), and (iv) assessments of motivation. Motivation was assessed following the first and final sessions.
Each session was structured into three phases: a standardized warm-up (15 minutes), a main instructional phase (40 minutes), and a cool-down period (5 minutes). The adapted program was tailored to the specific needs of adolescents with obesity by modifying drills, reducing competitiveness, and incorporating extended recovery and instructional periods. Pre-session videos in the ADAPT+VID group were uploaded to a private Facebook group 48 hours prior to each session and engagement was monitored.
The study received approval from the appropriate institutional ethics committee and was conducted in accordance with the Declaration of Helsinki. Written informed consent was obtained from all participants and their legal guardians prior to enrollment.
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55 participants in 3 patient groups
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Data sourced from clinicaltrials.gov
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