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Promoting Physical Activity In After-School Programs for Urban Adolescents

16 september 2013 bijgewerkt door: Montclair State University

Involving Adolescents in Physical Activity Promotion

RATIONALE: Physical activity may lower the risk of some types of cancer and other chronic diseases.

PURPOSE: This clinical trial is studying ways to increase physical activity in urban adolescents who attend after-school programs.

Studie Overzicht

Gedetailleerde beschrijving

OBJECTIVES:

Primary

  • Develop educational, promotional, and evaluation materials for use in promoting physical activity (PA) in community-based after-school programs by multiethnic, urban adolescents.
  • Develop a series of workshops for promoting physical activities (PAs) that are "a good fit" in after-school programs for these participants.
  • Determine a small set of feasibility tests as a first step towards pursuing funding for a full-scale experimental study.
  • Development of print materials for a series of skills-building workshops for these participants.
  • Development of evaluation materials, including self-report survey questions and structured interview protocols for qualitative assessment of participants' skills in identifying PAs that are a "good fit" for them.

OUTLINE: Youth participants will be assigned to one of two groups and may be involved in one or more research activities conducted during after-school hours at a community-based, after-school program site.

  • Focus group: Participants, consisting of 5-8 adolescents per focus group, either all male or all female, attend a single audiotaped focus group with a trained moderator for 60 minutes. Participants complete an anonymous participant information form, and explore their perceptions of physical activity (PA), perceptions of audience segments among peers that would be appropriate for tailoring physical promotions, and responses to images and graphic designs for use in developing print materials. Some participants may also be eligible to participate in a second focus group and the survey if interested.
  • One-on-one interview: Participants attend a one-on-one audiotaped individual interview with a trained interviewer for 60 minutes. Participants in the first set of interviews explore their perceptions of PA, their perceptions of the concept of finding PAs that are "a good fit", and their perceptions of audience segmentation for promoting PA. In the second set of interviews, participants test a protocol for qualitative assessment of adolescents' skills in assessing "good fit" of PA. Participants are involved in a series of visual and written scenarios depicting a variety of PAs, and use a structured interview format to identify the PA they most or least enjoy. Participants will also be asked to elaborate on criteria and experiences on which they based their decisions. Participants may also participate in the survey if interested.
  • Survey: Participants complete a paper and pencil 60-minute questionnaire about PA behaviors, attitudes, environments, and person-physical activity skills (i.e., skills in finding PAs that are "a good fit"). Two weeks later, participants are asked to complete a second questionnaire.
  • Key informant interview (adult): Participants attend a 60-minute, audiotaped interview with a trained interviewer that focuses on respondents' perceptions of the PA-related attitudes, behaviors, strengths, and barriers of the young adolescents who participate in their program, the respondents' experiences with promoting PA in their program participants, and respondents' suggestions for program elements and logistics to enhance the feasibility and effectiveness of after-school workshops to promote PA.
  • Workshop pilot testing: After data collection from the above field work is completed, 1-2 workshop activities are conducted in cooperation with program leaders at community-based, after-school programs.

PROJECTED ACCRUAL: Approximately 420 participants (400 adolescents and 20 adults) will be accrued for this study.

Studietype

Ingrijpend

Inschrijving (Verwacht)

420

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • New Jersey
      • Montclair, New Jersey, Verenigde Staten, 07043
        • Werving
        • Health and Nutrition Sciences at Montclair State University
        • Contact:
          • Amanda S. Birnbaum, PhD, MPH
          • Telefoonnummer: 973-655-7115

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

11 jaar tot 14 jaar (Kind)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

DISEASE CHARACTERISTICS:

  • Noninstitutionalized, community-residing youth living in and attending after-school programs in New York City or Newark, NJ OR
  • After-school program leaders at community agencies (i.e., adults) who participate in key informant interviews

PATIENT CHARACTERISTICS:

  • Any racial or ethnic background

PRIOR CONCURRENT THERAPY:

  • Not specified

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Preventie

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Behavior changes regarding physical activity by self-reported questionnaire

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Studie stoel: Amanda S. Birnbaum, PhD, MPH, Montclair State University

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start

1 september 2004

Primaire voltooiing (Verwacht)

1 augustus 2008

Studieregistratiedata

Eerst ingediend

8 maart 2006

Eerst ingediend dat voldeed aan de QC-criteria

8 maart 2006

Eerst geplaatst (Schatting)

10 maart 2006

Updates van studierecords

Laatste update geplaatst (Schatting)

17 september 2013

Laatste update ingediend die voldeed aan QC-criteria

16 september 2013

Laatst geverifieerd

1 juni 2009

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • CDR0000455588
  • MSUHNS-0003669
  • FWA00005270

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

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