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Promoting Physical Activity In After-School Programs for Urban Adolescents

16 de septiembre de 2013 actualizado por: 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.

Descripción general del estudio

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Anticipado)

420

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • New Jersey
      • Montclair, New Jersey, Estados Unidos, 07043
        • Reclutamiento
        • Health and Nutrition Sciences at Montclair State University
        • Contacto:
          • Amanda S. Birnbaum, PhD, MPH
          • Número de teléfono: 973-655-7115

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

11 años a 14 años (Niño)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Todos

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Behavior changes regarding physical activity by self-reported questionnaire

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Silla de estudio: Amanda S. Birnbaum, PhD, MPH, Montclair State University

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de septiembre de 2004

Finalización primaria (Anticipado)

1 de agosto de 2008

Fechas de registro del estudio

Enviado por primera vez

8 de marzo de 2006

Primero enviado que cumplió con los criterios de control de calidad

8 de marzo de 2006

Publicado por primera vez (Estimar)

10 de marzo de 2006

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

17 de septiembre de 2013

Última actualización enviada que cumplió con los criterios de control de calidad

16 de septiembre de 2013

Última verificación

1 de junio de 2009

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • CDR0000455588
  • MSUHNS-0003669
  • FWA00005270

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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