Peer Education, Exercising and Eating Right - Obesity Prevention in Freshmen Women

NCT ID: NCT01043614

Last Updated: 2010-01-07

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

300 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-08-31

Study Completion Date

2010-05-31

Brief Summary

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

Project PEER utilizes a randomized controlled study design to investigate the combined effects of an exercise and nutrition intervention that is based on self-efficacy principles and delivered primarily by peer educators to reduce the risk for obesity in female college freshman over one academic year (N = 300). The control group will receive minimal interaction from the research team, paralleling the typical freshman experience on the UIUC campus. Recruitment will take place in two waves (consecutive fall terms with n = 150).

During the final year (Fall 2010) of the project, a General Education course will be offered that targets weight management. Importantly, the discussion groups for this course will be taught by peer educators trained using the peer resources further refined during the PEER project. In addition to conventional measures of content knowledge assessed in the college classroom when obtaining class credit, personal physical activity and nutrition behaviors along with behavioral determinants (self-efficacy, self-regulatory skills and outcome expectations) will also be assessed.

Primary Aim 1: To determine the effectiveness of a peer-delivered self efficacy-based behavioral intervention to enhance nutrition and physical activity behaviors and subsequently weight management success in female university freshman over one academic year. We hypothesize that freshmen randomized to the intervention group will be more successful in losing or maintaining weight than the control group through a combination of diet and physical activity strategies.

Primary Aim 2: To examine the role played by social cognitive factors in changing nutrition and physical activity behaviors across one academic year. We hypothesize that self-efficacy will have both a direct influence on behavior and an indirect effect through its influence on self-regulatory skills and outcome expectations.

Detailed Description

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

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.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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

Peer group education

Small groups of female college freshmen facilitated by peer educators

Group Type EXPERIMENTAL

PEER group intervention

Intervention Type BEHAVIORAL

An exercise and nutrition intervention that is based on self-efficacy principles and delivered primarily by peer educators to reduce the risk for obesity in female college freshman over one academic year

Interventions

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

PEER group intervention

An exercise and nutrition intervention that is based on self-efficacy principles and delivered primarily by peer educators to reduce the risk for obesity in female college freshman over one academic year

Intervention Type BEHAVIORAL

Eligibility Criteria

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

Inclusion Criteria

* Female
* In first year on campus, enrolled full-time, and in residence on the UIUC campus
* Aged 17-19 yrs (minors will be required to obtain parental signature on the IRB form)
* Free from any chronic disease/condition that would alter ability to exercise or preclude diet manipulation such as diabetes, hypertension or pregnancy.
* Free from an eating disorder as assessed using the Eating Disorder Inventory
* Free from any medications that would alter adiposity or psychological outcomes
* Sedentary or participation in non-professional recreational activity
* Non-smoking
* Body mass index (BMI) between the 50th and 95th BMI-for-age percentile

Exclusion Criteria

* Male
* Status other than freshman or enrolled for entire year
* Not living on campus
* Smoking
* Pregnant
* Competitive athlete
* Chronic condition that would alter ability to exercise or preclude diet manipulation such as diabetes, hypertension
* Eating disorder as assessed using the Eating Disorder Inventory
* Taking medications that would alter adiposity or psychological outcomes
* Participation in competitive athletics
* BMI outside parameters
Minimum Eligible Age

17 Years

Maximum Eligible Age

19 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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

University of Illinois at Urbana-Champaign

OTHER

Sponsor Role lead

Responsible Party

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

University of Illinois at Champaign-Urbana

Principal Investigators

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

Ellen M Evans, PhD

Role: PRINCIPAL_INVESTIGATOR

Uiversity of Illinois at Urbana- Champaign

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University of Illinois at Urbana-Champaign

Urbana, Illinois, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

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

2007-04574

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

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

Black Women's Wellness Project
NCT04063059 COMPLETED NA
Weight Gain Prevention
NCT00606840 COMPLETED NA
BfedBwell Proof-of-Concept Pilot
NCT06191666 ACTIVE_NOT_RECRUITING NA