- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01043614
Peer Education, Exercising and Eating Right - Obesity Prevention in Freshmen Women (ProjectPEER)
Project PEER: Peer Education, Exercising and Eating Right
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.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Voraussichtlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Illinois
-
Urbana, Illinois, Vereinigte Staaten, 61801
- University of Illinois at Urbana-Champaign
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
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
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Peer group education
Small groups of female college freshmen facilitated by peer educators
|
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
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Anthropometric measures (eg; weight, hip/ waist dimensions)
Zeitfenster: Baseline, 3 mo, 8 mo, 1 y and 2 y follow up
|
Baseline, 3 mo, 8 mo, 1 y and 2 y follow up
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Self-efficacy measures for physical activity, nutrition
Zeitfenster: Baseline, 3 mo, 8 mo, 1 y and 2 y follow up
|
Baseline, 3 mo, 8 mo, 1 y and 2 y follow up
|
Mitarbeiter und Ermittler
Ermittler
- Hauptermittler: Ellen M Evans, PhD, Uiversity of Illinois at Urbana- Champaign
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Voraussichtlich)
Studienabschluss (Voraussichtlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 2007-04574
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .