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Completed No phase listed Observational

Influence of Parents and Friends on Children and Adolescents

ClinicalTrials.gov ID: NCT00875576

Public ClinicalTrials.gov record NCT00875576. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 1:37 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to directly compare the effects of parents and friends on overweight and non-overweight children and adolescents' food intake and food selection using a cross-sectional design. Overweight and non-overweight children (5-6 year-old) and adolescents (13-14 year-old) will share a meal with a friend and with a parent on separate occasions. Participants' food selection and the amount of food they consumed will be compared across conditions. Hypothesis 1: The investigators hypothesize that overweight children and adolescents will select more unhealthy food items and eat more in the presence of an overweight friend than when eating with a lean friend; whereas lean participants eating with an overweight friend will eat a similar amount of food than lean youth eating with a lean friend. Hypothesis 2: The investigators predict that overweight children and adolescents (but not lean children and teens) will consume more food in the presence of their mother than in the presence of a friend. Hypothesis 3: The investigators also predict that overweight youth's energy intake will be related to parental prompts. Hypothesis 4: The investigators expect greater similarities in terms of food selection and food intake between adolescents and their friend than between adolescents and their parent.

Study identification

NCT ID
NCT00875576
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
University at Buffalo
Other
Enrollment
40 participants

Conditions and interventions

Conditions

Interventions

Not listed

Eligibility (public fields only)

Age range
5 Years to 14 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2008
Primary completion
May 31, 2010
Completion
May 31, 2010
Last update posted
Jun 27, 2010

2009 – 2010

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
University at Buffalo, Division of Behavioral Medicine Buffalo New York 14214

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00875576, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 27, 2010 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00875576 live on ClinicalTrials.gov.

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