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Healthy Living in Overweight and Obese Adolescents ASGE-FABES Program in Development of Formats

NCT04794244 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2021-03-12

No results posted yet for this study

Summary

The aim of this project is to develop multiple behavioral strategies for the prevention of obesity in adolescents.

ASGE-FABES \[Adolescent Health Promotion Physical Activity, Physical activity of overweight and obese youth of Nutrition, Stress Management\] Program,to evaluate its effects on nutrition and mental health. Program overweight and obeseadolescents to lose weight in a healthy way, healthy lifestyle behaviors make healthy choices, nutritional and physical activity knowledgecognitive and It aims to gain behavioral skills. In the study, "pretest-posttest in randomized groupswith control group, with repeated measures \& quot; experimental design type is used. The sample of the research,250 (125-experiment, 125-control) constituted an overweight and obese adolescent.

Conditions

  • Healthy Lifestyle Behaviors
  • Overweight Adolescents
  • Obese Adolescents

Interventions

BEHAVIORAL

ASGE-FABES Program

In the control group study, pretest-posttest and experimental design with repeated measurements were used in randomized groups. An overweight and obese adolescent constituted the sample of 250 (125-experiment, 125-control) of the study. Research data Socio-Demographic Features Information Form, Adolescent Nutrition Information Scale, Adolescent Physical Activity Information Scale, Adolescent Lifestyle Scale, Healthy Lifestyle Choice Scale for Adolescents, Beck Anxiety Scale, Daily Food Consumption Form, Beverage Consumption Form, collected using. Data are saved before and after application. ASGEFABES PROGRAM was applied to the experimental group for 10 weeks. Measurements after the training program were collected in four measurements: 1st week, 6th and 12th months.

Sponsors & Collaborators

  • aysun ardıç

    lead OTHER

Principal Investigators

  • aysun ARDIÇ, Ph.D · Istanbul University - Cerrahpasa

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
11 Years
Max Age
12 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-09-20
Primary Completion
2017-12-20
Completion
2019-07-09

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04794244 on ClinicalTrials.gov