Department of Internal Medicine and VCU Massey Cancer Center, Virginia Commonwealth University, 1200 East Broad Street, P.O. Box 980306, Richmond, VA 23298, USA.
Prev Med. 2012 Feb;54(2):150-6. doi: 10.1016/j.ypmed.2011.11.005. Epub 2011 Dec 3.
We implemented a theory-based randomized controlled trial (Living Free of Tobacco, Plus (LIFT+) in ten rural middle schools and assessed impact on tobacco use and fruit/vegetable (F/V) intake in 2008-2010. Data on F/V intake at baseline, immediate post intervention, and 1-year follow-up are presented.
Schools were randomized to intervention or control groups. Goal setting, peer leaders, and class workshops with parent involvement, were intervention features; community partners were supportive. Seventh graders filled out surveys on health behaviors, psycho-social variables, and demographic characteristics. Adjusted models comparing intervention and control conditions were analyzed.
Sample (n=1119) was 48.5% female, 50% White, with a mean age of 12.7 years. Mean F/V servings were significantly higher in intervention schools at immediate post (3.19 servings) and at 1-year (3.02 servings) compared to controls (2.90, 2.69 respectively). Knowledge of 5-a-day recommendation was significantly higher in intervention schools at immediate post test (75.0%) versus controls (53.8%) but not at 1-year follow-up.
Intervention schools reported significantly higher mean F/V servings at post intervention and 1-year, and for knowledge of F/V recommendations at immediate post compared to controls. Higher levels of parent and community involvement may further increase F/V intake in future interventions. ClinicalTrials.gov Identifier: NCT01412697.
我们在十所农村中学实施了一项基于理论的随机对照试验(LIFT+),评估了其对 2008-2010 年期间烟草使用和水果/蔬菜(F/V)摄入量的影响。本文呈现了基线、即时干预后和 1 年随访时 F/V 摄入量的数据。
学校被随机分为干预组和对照组。目标设定、同伴领导、有家长参与的班级研讨会,是干预的特点;社区合作伙伴提供支持。七年级学生填写了关于健康行为、心理社会变量和人口特征的调查。对干预和对照条件进行了调整模型分析。
样本(n=1119)中,女性占 48.5%,白人占 50%,平均年龄为 12.7 岁。干预组在即时后(3.19 份)和 1 年后(3.02 份)的 F/V 摄入量明显高于对照组(分别为 2.90 份和 2.69 份)。即时后测试中,干预组对 5-a-day 推荐量的知晓率明显高于对照组(75.0%对 53.8%),但在 1 年后的随访中则不然。
干预组在即时后和 1 年后报告的 F/V 平均摄入量更高,对 F/V 推荐量的知识也更高,即时后测试中,干预组对 5-a-day 推荐量的知晓率明显高于对照组。未来的干预措施中,家长和社区更高水平的参与可能会进一步增加 F/V 的摄入量。临床试验注册号:NCT01412697。