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Neighborhood Influence on Parenting Practices Regarding Youth Outdoor Play

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ClinicalTrials.gov Identifier: NCT03379090
Recruitment Status : Enrolling by invitation
First Posted : December 20, 2017
Last Update Posted : April 4, 2018
Sponsor:
Collaborator:
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Information provided by (Responsible Party):
Maura Kepper, Pennington Biomedical Research Center

Brief Summary:
Parental constraint of outdoor play may be fueling unhealthy emotional and physical development in today's children and adolescents. Time spent outdoors is a key determinant of unstructured play and overall physical activity levels, both of which are crucial to optimal development in youth. Modern barriers - such as crime, poor social ties among neighbors, and unsafe physical environments - constrain parental practices and reduce opportunities for outdoor play in children and youth. Low levels of perceived collective efficacy, a measure of perceived neighborhood cohesion and the collective capacity to solve neighborhood problems, has been proposed as a social environmental factor that constrains outdoor play by parents either attempting to avoid potentially dangerous situations or using defensive behavior by upgrading security measures. Moreover, incivilities in the neighborhood physical environment (e.g. litter, graffiti, blighted property) may influence parents' perceived collective efficacy. Consequently, a child's ability to achieve the recommended minimum of 60 minutes of daily physical activity may be limited by a complex interaction between neighborhood social and physical environmental factors and the extent to which parents respond by constraining offspring outdoor play. The central hypothesis of this research is that modifiable factors in the neighborhood social and physical environment result in parental constraint of offspring outdoor play, which reduces overall physical activity during critical years of development. This research will use qualitative methods to generate a comprehensive understanding of how and which environmental factors play a crucial role in parental constraint of outdoor play and promote low levels of within-neighborhood physical activity. This ancillary study will recruit 32 parents/guardians of participants from the parent study, Translational Investigation of Growth and Everyday Routines in Kids (TIGER Kids) Study (USDA 3092-51000-056-04A), to participate in in-depth interviews. My ultimate goal is to use knowledge gained from this ancillary study to generate community-based interventions that will target neighborhood factors to successfully reduce parental constraints on outdoor play.

Condition or disease
Physical Activity Adolescent Behavior Parenting

Study Type : Observational
Estimated Enrollment : 32 participants
Observational Model: Case-Only
Time Perspective: Cross-Sectional
Official Title: Using In-depth Interviews to Examine Neighborhood Influence on Parenting Practices Regarding Youth Outdoor Play and Physical Activity.
Actual Study Start Date : March 26, 2018
Estimated Primary Completion Date : December 7, 2018
Estimated Study Completion Date : August 6, 2019

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Parenting




Primary Outcome Measures :
  1. Perceptions of how the social environment influences parenting practices related to outdoor play and youth's physical activity. [ Time Frame: One time-point, 1 hour in-depth interview ]
    Indepth interviews will be used to measure parental perceptions of how the social environment in which they live influences their parenting decisions regarding their child's outdoor play.



Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population
32 parents/guardians of participants from the TIGER Kids parent study will be recruited for this study. All parents/guardians will be recruited after their child has completed the baseline (Y0) TIGER Kids study visit.
Criteria

Inclusion Criteria:

-Child completed baseline measures (Y0) for the parent study, TIGER Kids Study (USDA 3092-51000-056-04A).

Exclusion Criteria:

  • Child did not complete baseline measures (Y0) of the TIGER Kids Study.
  • Did not report a home address at the baseline (Y0) TIGER Kids study visit.
  • Unwilling or unable to participate in an in-depth interview.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03379090


Locations
United States, Louisiana
Pennington Biomedical Research Center
Baton Rouge, Louisiana, United States, 70808
Sponsors and Collaborators
Pennington Biomedical Research Center
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
Investigators
Principal Investigator: Maura Kepper, PhD Pennington Biomedical Research Center
  Study Documents (Full-Text)

Documents provided by Maura Kepper, Pennington Biomedical Research Center:
Informed Consent Form  [PDF] April 6, 2017


Responsible Party: Maura Kepper, Postdoctoral Fellow, Pennington Biomedical Research Center
ClinicalTrials.gov Identifier: NCT03379090     History of Changes
Other Study ID Numbers: 2017-017-PBRC
1F32HD093282-01 ( U.S. NIH Grant/Contract )
First Posted: December 20, 2017    Key Record Dates
Last Update Posted: April 4, 2018
Last Verified: April 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Plan Description: There is currently no plan to share IPD. Qualitative data may be difficult to prepare to ensure privacy of the participant. Furthermore, we do not see the benefit of sharing IPD from this study as qualitative data cannot be easily reanalyzed to validate study findings, combined with other datasets, and has a high risk of being analyzed using invalid/non-rigorous methods.

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No