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Completed

NCT Number: NCT02453269

Transdisciplinary Program Against Childhood Obesity

The purpose of this study was to evaluate the outcome of a 1-year transdisciplinary program against childhood obesity.

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Key information

Age range

7 year–11 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Carminda Maria Goersch Fontenele Lamboglia

Fortaleza, Ceará, 60.811-905, Brazil

About this study

The study was quasi-experimental with a quantitative approach.5 Epidemiologically, the study may be characterized as a controlled, randomized trial. Twenty participants were selected non-randomly from an elementary school in Fortaleza, Brazil. The parents or caretakers of the participants gave their informed written consent. The 20 participants were distributed randomly into two groups, G1 (intervention, n=10) and G2 (control, n=10). Six children did not complete the study protocol: three in G1 due to insufficient attendance, and three in G2 for unspecified reasons. To be eligible for the study, children should i) be overweight or obese in accordance with the definition given above6, ii) be considered healthy by a physician after undergoing a clinical examination, iii) attend the transdisciplinary intervention sessions once a week (minimum attendance required: 90%) and iv) be authorized to participate by their parents or caretakers. The children in the control group were not submitted to the intervention and were not participating in any other program involving obesity control or supervised physical activity. All children (G1+G2) were instructed to maintain their habitual level of physical activity and attend the school's regular physical education classes. The latter were scheduled twice a month during the first term and four times a month during the second. The decision to increase the frequency was made by the school's director in acknowledgment of the importance of physical activity, but the change affected the two groups equally. Children were ineligible if they had chronic diseases (defined as diseases requiring continuous therapy), mental disorders or cognitive impairments which might interfere with communication, or used a pacemaker, or declined participation. Children in G1 missing more than 10% of the total intervention sessions were excluded from the sample. The study was conducted at an elementary school in Fortaleza, Brazil, maintained by the Edson Queiroz Foundation/UNIFOR. Data were collected at baseline in May 2013 (pre-test) and after one year of intervention, in May 2014 (post-test), as part of the transdisciplinary program against childhood obesity. Children in G1 were submitted to a transdisciplinary intervention once a week. Each child received a nutritional education kit including four games ("Cool Diet", a board game, a memory game and a word search puzzle) and an interactive booklet containing illustrations of foods selected from the participants' cultural context (Northeastern Brazil). The kit was validated by Munguba. The children in the control group (G2) were not exposed to interventions during the study period. They attended the school's regular physical education classes, but were excluded from the sample if they joined any other physical activity or weight control program. At the end of the study, the children in G2 received the booklet described above, including the results of the physical fitness evaluation. Talks about the importance of physical activity and healthy food in this group were scheduled for early 2015. Upon the first visit, all participants were given a physical evaluation (BMI, height and waist circumference) following the procedures standardized by Lohman, Roche and Martorell. The body composition was determined by bioelectrical impedance (Bodystat 1500 MMD) upon the second visit. Upon the first, the children were instructed in how to prepare for the test: abstain from food and drink (4 hours before), exercise (12 hours before), alcohol (24 hours before) and diuretic medication (7 days before), and urinate 30 min before the test. The subject is measured lying down, with electrodes attached to hands and feet. The muscular fitness assessment was based on FitnessGram®, a criterion-referenced test, but was limited to flexibility and abdominal muscle strength/endurance. The evaluation of sexual maturity was based on the age at menarche in girls and on armpit hair development in boys. The purpose of this evaluation was to identify each participant's stage of growth, development and maturity.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • To be eligible for the study, children should
  • be overweight or obese in accordance with the definition given above6,
  • be considered healthy by a physician after undergoing a clinical examination,
  • attend the transdisciplinary intervention sessions once a week (minimum attendance required: 90%)
  • be authorized to participate by their parents or caretakers.
  • The children in the control group were not submitted to the intervention and were not participating in any other program involving obesity control or supervised physical activity.
  • All children (G1+G2) were instructed to maintain their habitual level of physical activity and attend the school's regular physical education classes.
  • The latter were scheduled twice a month during the first term and four times a month during the second.
  • The decision to increase the frequency was made by the school's director in acknowledgment of the importance of physical activity, but the change affected the two groups equally.

Exclusion criteria

  • Children were ineligible if they had chronic diseases (defined as diseases requiring continuous therapy), mental disorders or cognitive impairments which might interfere with communication, or used a pacemaker, or declined participation.
  • Children in G1 missing more than 10% of the total intervention sessions were excluded from the sample.

Treatment and study plan

Transdisciplinary program

Behavioral

Primary outcomes

  1. Height (cm) (outcome)

    Time frame: Participants were followed for the duration of one year

  2. Body mass (kg) (outcome)

    Time frame: Participants were followed for the duration of one year

  3. Body mass index (kg/m2) (outcome)

    Time frame: Participants were followed for the duration of one year

  4. Waist circumference (cm) (outcome)

    Time frame: Participants were followed for the duration of one year

  5. Waist circunference/height ratio (outcome)

    Time frame: Participants were followed for the duration of one year

  6. Body fat percentage (%) (outcome)

    Time frame: Participants were followed for the duration of one year

  7. Fat body mass (kg) (outcome)

    Time frame: Participants were followed for the duration of one year

  8. Lean body mass (kg) (outcome)

    Time frame: Participants were followed for the duration of one year

  9. Abdominal strength (repetition) (outcome)

    Time frame: Participants were followed for the duration of one year

  10. Flexibility (cm) (outcome)

    Time frame: Participants were followed for the duration of one year

Sponsors and collaborators

Lead sponsor

Fortaleza University

Other

Registry information

Official study title

Outcome of a 1-year Transdisciplinary Program Against Childhood Obesity

Acronym: OTPACO

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
May 25, 2015
Registry last updated
May 25, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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