Elsevier

Addictive Behaviors

Volume 18, Issue 1, January–February 1993, Pages 51-56
Addictive Behaviors

Demographic, psychosocial and behavioral differences in samples of actively and passively consented adolescents

https://doi.org/10.1016/0306-4603(93)90008-WGet rights and content

Abstract

Requiring active consent from parents leads to different self-reports by adolescents than when it is not required. The present study compares self-reported demographic, psychosocial, and behavior variables between those students from whom active consent was and was not obtained. As found in previous studies, fewer minorities, fewer persons who were dissatisfied with school, fewer persons whose parents were of lower educational levels, and fewer cigarette smokers were represented in the sample recruited by active parental consent. Extending on previous work, we found those students whose parents failed to respond to the consent procedure were less likely to live with both parents, were more likely to be latch-key children, placed a lower priority on health, and were higher in risk-taking, lower in self-esteem, and lower in assertiveness than those whose parents had responded. These data further support the suggestion that those children who are omitted from a research study because of lack of action on the part of the parent are at higher risk for a number of health and social problems. These children need to be included in evaluation samples in order to accurately assess the effectiveness of prevention programming. Future studies should employ a passive consent procedure as a means of recruiting a representative subject pool in school-based prevention research.

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Cited by (89)

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    The low-response rates reported in active consent studies reflect a systematic bias of sampling in a way that over-represents some portions of the population while under-representing others. For example, active consent procedures yielded study samples that over-represented female and Caucasian students [15,16] and students with high academic achievement [10], and under-represented minority groups such as African-American and Asian American students, Hispanic youth [9,17], children who were low achievers, and children whose parents were less well-educated [15,16]. Significant differences between respondents and nonrespondents may also emerge in the prevalence of risk behaviors when active consent procedures are used [12,17].

  • Measuring Success: Evaluation Designs and Approaches to Assessing the Impact of School-Based Health Centers

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    Although this manuscript was not structured as a systematic review, an example of each approach in practice is also provided. Suboptimal participation rates—both in terms of absolute numbers and representativeness—introduce the possibility of bias and have been documented as a challenge [35,44–46]. Through planning, coordinating with school events, and collaborating with teachers and administrators, researchers can work to obtain high, representative rates of participation while adhering to ethical principles [13], regardless of the format by which parental permission is solicited (i.e., active or passive “opt-out”).

  • The association between peer victimization and functioning at school among urban Latino children

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    The small sample size was partially due to the relatively low overall positive consent rate and the students who took part in the study may be more academically engaged than their non-participating peers. Researchers typically have difficulty obtaining parental consent when conducting school-based research (Fletcher & Hunter, 2003) and the problems appear to be magnified in schools with children from low SES backgrounds (Dent et al., 1993). Measuring all of the variables concurrently is another major limitation of the current study.

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This research was supported by a grant from the National Cancer Institute (CA#44907) awarded to S. Sussman, C.W. Dent, D. Burton, A. Stacy, and B.R. Flay.

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