Get in the GROOVE! (GROOVE)
20. Februar 2017 aktualisiert von: Patrice G. Saab, University of Miami
Get in the GROOVE (Girls Realizing Options Through OpenSim Virtual Experiences)!
Get in the GROOVE! will address health disparities impacting underserved youth. Given the alarming rate of overweight and obesity among high school minority youth, the project will focus on middle school with the primary aim of reaching middle school girls before unhealthy habits become firmly ingrained.
The primary aim of the research project is to investigate the impact of two types of summer science enrichment programs (that focus on health and wellness) on middle school girls' self-efficacy, health knowledge, health behaviors, and interest in science. One program will present the curriculum by conventional means (GROOVE condition) while the second program will include the addition of a closed 3-D virtual world environment to reinforce concepts (GROOVE+ condition).
The following hypotheses will be tested in the randomized controlled trial:
- Upon completion of the summer program, the enhanced summer program GROOVE+ relative to the conventional summer program will result in a) increased self-efficacy for adopting healthy behavior change; b) increased health knowledge; c) enhanced science self-concept; and e) more positive behavior change (e.g., improved nutrition, increased physical activity).
- At follow-up, the enhanced summer program relative to the conventional summer program will result in further and/or sustained improvements in positive behavior health behaviors and attitudes.
Studienübersicht
Status
Abgeschlossen
Bedingungen
Studientyp
Interventionell
Einschreibung (Tatsächlich)
375
Phase
- Unzutreffend
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienorte
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Florida
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Miami, Florida, Vereinigte Staaten, 33129
- Patricia and Phillip Museum of Science
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New York
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Queens, New York, Vereinigte Staaten, 11368
- New York Hall of Science
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Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
11 Jahre bis 14 Jahre (Kind)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Weiblich
Beschreibung
Inclusion Criteria:
- Girls 11-14 years old
Exclusion Criteria:
Girls are excluded if they are:
- not fluent in English
- enrolled in a special education program at school (other than gifted program) that would interfere with ability to master the material
- have a condition that would preclude their participation in the dance activities of the summer program
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
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Aktiver Komparator: Summer wellness program - nutrition & physical activity
The GROOVE condition uses conventional means to address health-related activities and content within the context of a science museum summer enrichment program.
The emphasis is on nutrition, physical activity, and healthy lifestyle.
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The enhanced virtual world education (GROOVE+) will be compared to conventional approach (GROOVE).
Each program is Monday-Friday, 9:30-3:30, for 3 weeks in the summer.
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Experimental: Summer program plus virtual world technology
The GROOVE+ condition enhances the conventional approach to address health-related activities and content within the context of a science museum summer enrichment program by employing technology and a 3-D virtual world as a key educational strategy.
The emphasis is on nutrition, physical activity, and healthy lifestyle.
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The enhanced virtual world education (GROOVE+) will be compared to conventional approach (GROOVE).
Each program is Monday-Friday, 9:30-3:30, for 3 weeks in the summer.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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change in Health Knowledge
Zeitfenster: pretreatment ( Day1-2) and post treatment (end of 3 week summer session)
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Multiple choice questionnaire used to assess participants' health knowledge pertaining to nutrition, physical activity, weight, and lifestyle.
The measure will test for the content of the summer program.
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pretreatment ( Day1-2) and post treatment (end of 3 week summer session)
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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change in Self-efficacy - physical activity
Zeitfenster: pretreatment ( Day1-2) and post treatment (end of 3 week summer session)
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The physical activity self-efficacy support seeking and barriers subscales developed by Saunders, Pate, Felton et al.'s (1997, Preventive Medicine, vol.
26, 241-247) will be used.
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pretreatment ( Day1-2) and post treatment (end of 3 week summer session)
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change in Self-efficacy - fruit and vegetable consumption
Zeitfenster: pretreatment ( Day1-2) and post treatment (end of 3 week summer session)
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The food-related self-efficacy scale items comes from the work of Reynolds et al. ( 2002, Health Psychology, vol.
21, 51-60) and addresses fruit and vegetable consumption.
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pretreatment ( Day1-2) and post treatment (end of 3 week summer session)
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change in Self-efficacy - science
Zeitfenster: pretreatment ( Day1-2) and post treatment (end of 3 week summer session)
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Science self-efficacy assesses confidence to master the GROOVE program science components.
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pretreatment ( Day1-2) and post treatment (end of 3 week summer session)
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Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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change in health behaviors
Zeitfenster: pretreatment ( Day1-2), post treatment (end of 3 week summer session), and up to a year follow-up
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eating habits and physical activity habits
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pretreatment ( Day1-2), post treatment (end of 3 week summer session), and up to a year follow-up
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change in Science attitudes and aspirations
Zeitfenster: pretreatment ( Day1-2), post treatment (end of 3 week summer session), and up to a year follow-up
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This measure consist of items drawn from Louise Archer et al.'s (2013, Journal of Education Policy, 1-28, http://www.tandfonline.com/doi/abs/10.1080/02680939.2013.790079#.UbDmUuARtm1) ASPIRES project.
Participants are asked to make ratings reflecting science attitudes, aspirations, and interests.
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pretreatment ( Day1-2), post treatment (end of 3 week summer session), and up to a year follow-up
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change in Family and participant habits
Zeitfenster: pretreatment ( Day1-2), post treatment (end of 3 week summer session - for participant only), and up to a year follow-up
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Assesses family and participant activities and habits and ratings of participant health and interests.
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pretreatment ( Day1-2), post treatment (end of 3 week summer session - for participant only), and up to a year follow-up
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change in Pedometer activity
Zeitfenster: Participants will be given a pedometer to wear during the 3 week summer program period
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Pedometers will be used daily to assess physical activity.
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Participants will be given a pedometer to wear during the 3 week summer program period
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Change in eating behavior
Zeitfenster: Up to 4 assessments will occur over the 3 week program.
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The Eating Behavior Scale consists of 28 items; all 20 items from Fahlman et al. (2013, American Journal of Health Education, vol.
43, 165-171) and 8 additional items from the 2009-2010 School Physical Activity and Nutrition Project (https://sph.uth.edu/content/uploads/2011/12/SPAN_2009-10_8th-11thStudentSurveyEnglish_FINAL.pdf).
The measure asks participants to indicate how many times they consumed an item on the day before (e.g., fruits, vegetables, candy, etc).
A subsample of students will complete up to three 24-hour dietary recalls to examine the validity of the self-report items in the study's participants.
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Up to 4 assessments will occur over the 3 week program.
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change in Presence
Zeitfenster: up to 3 times during the GROOVE+ condition
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The presence scale consists of 11 items influenced by the work of Fox et al. (2009, Presence Vol.
18,294-303) will be completed by the participants in the GROOVE+ condition.
The scale assesses the extent to which the participant feels present in the 3-D virtual world.
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up to 3 times during the GROOVE+ condition
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Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Mitarbeiter
Ermittler
- Hauptermittler: Patrice G Saab, Ph.D., University of Miami
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn
1. Mai 2013
Primärer Abschluss (Tatsächlich)
1. September 2016
Studienabschluss (Tatsächlich)
1. Januar 2017
Studienanmeldedaten
Zuerst eingereicht
30. Juni 2014
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
10. Juli 2014
Zuerst gepostet (Schätzen)
11. Juli 2014
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
23. Februar 2017
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
20. Februar 2017
Zuletzt verifiziert
1. Februar 2017
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Andere Studien-ID-Nummern
- 20111081
- 5R25OD010525 (US NIH Stipendium/Vertrag)
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
Produkt, das in den USA hergestellt und aus den USA exportiert wird
Nein
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 .
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