Transdisciplinary Program Against Childhood Obesity (OTPACO)
Outcome of a 1-year Transdisciplinary Program Against Childhood Obesity
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Ceará
-
Fortaleza, Ceará, Brazil, 60.811-905
- Carminda Maria Goersch Fontenele Lamboglia
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Transdisciplinary program
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).
|
|
|
No Intervention: Control group
The children in the control group (G2) were not exposed to interventions.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Height (cm) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Body mass (kg) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Body mass index (kg/m2) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Waist circumference (cm) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Waist circunference/height ratio (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Body fat percentage (%) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Fat body mass (kg) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Lean body mass (kg) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Abdominal strength (repetition) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
|
Flexibility (cm) (outcome)
Time Frame: Participants were followed for the duration of one year
|
Participants were followed for the duration of one year
|
Collaborators and Investigators
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- TRANS 123
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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