Overweight, Quality of Life and Psychological Difficulties in Teenagers

NCT ID: NCT02417909

Last Updated: 2015-08-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

173 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-07-31

Study Completion Date

2015-07-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Obesity is a major public heath issue. It may have various impacts on a patient's life by causing psychological problems, altering a patient's quality of life,etc. These led to the investigators' hypothesis which is examining the psychological dimensions of a teenager suffering for obesity.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

There are two groups in this study : healthy volunteers and teenagers suffering from obesity.

Patients and healthy volunteers will come to the nutrition clinic center Naturalpha where the patient will complete a questionnaire. The included patients will also complete a questionnaire privately (without the presence of the parents), they will also be weighted and measured.

No further tests or questionnaires will be given after the enrollment day.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Obesity

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Healthy volunteers

This group is composed of healthy teenagers that volunteered to participate in the trial and that will answer questionnaires about quality of life. Parents will anwser questionnaires too.

questionnaires about quality of life

Intervention Type OTHER

all teenagers included in the trial and their parents must complete the questionnaires given of them the day of enrollment.

Obese teenagers

This group is composed of obese teenagers that have been recruited to participate in the trial and that will answer different questionnaires quality of life. Parents will anwser questionnaires too.

questionnaires about quality of life

Intervention Type OTHER

all teenagers included in the trial and their parents must complete the questionnaires given of them the day of enrollment.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

questionnaires about quality of life

all teenagers included in the trial and their parents must complete the questionnaires given of them the day of enrollment.

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients aged between 11 and 16 years old at the moment of enrollment.
* Body Mass Index between the 1st and 2nd degree of the obesity zone (over the 97th percentile curve regarding corpulence curves of the Plan National Nutrition Santé (PNNS) based on the gender (boys/girls))
* The teenagers have an appointment in the pediatric unit of the Saint Vincent de Paul Hospital for an examination regarding excess weight


* Patients aged between 11 and 16 years old at the moment of enrollment
* Body Mass Index located between the 3rd and the 97th percentile on the corpulence curves of the PNNS
* The teenagers and their parents have replied to and advertisement of the trial

Exclusion Criteria

* Body Mass Index over the 97th percentile curve on the corpulence curves of the PNNS
* Handicapped teenagers


* Body Mass Index over the 97th percentile curve or under the 3rd percentile curve on the corpulence curves of the PNNS
* Handicapped, asthmatic, obese or diabetic teenagers
Minimum Eligible Age

11 Years

Maximum Eligible Age

16 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Lille Catholic University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Gronnier Pascale, MD

Role: PRINCIPAL_INVESTIGATOR

Groupment des Hôpitaux de l'Institut Catholique de Lille

Gueorguieva Iva, MD

Role: PRINCIPAL_INVESTIGATOR

Centre Hospitalier Universitaire de Lille

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

RC-P0011

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Pediatric Obesity Management Study
NCT05622981 TERMINATED NA
Lille Study for Childhood Health Promotion
NCT05121090 NOT_YET_RECRUITING