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Child Behavior clinical trials

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NCT ID: NCT02091154 Completed - Health Behavior Clinical Trials

How Environmental Interventions Influence Behavior in School Lunchrooms

Start date: March 2012
Phase: N/A
Study type: Interventional

The investigators hypothesize that the new United States Department of Agriculture (USDA) regulations for lunches served as part of the National School Lunch Program will decrease the percentage of enrolled students purchasing lunch, increase the percentage of children taking fruit and vegetables, decrease the percentage of fruit and vegetable servings being thrown away, and increase the total number of fruit and vegetable servings eaten. The investigators also hypothesize that when the regulations are in force, simple behavioral interventions can counteract the potentially negative impact on lunch sales and consumption. In other words, implementing the regulations and behavioral interventions together, the percentage of enrolled students taking a school lunch will increase at least back to baseline levels, the percentage of children taking fruits and vegetables will increase, the percentage of fruit and vegetable servings wasted will decrease, and the total number of fruit and vegetable servings eaten will increase.

NCT ID: NCT01802294 Completed - Parenting Clinical Trials

Sinovuyo Caring Families Project - Pilot Trial

SCFP
Start date: February 2013
Phase: Phase 1
Study type: Interventional

This pilot feasibility trial will evaluate the Sinovuyo Caring Families Program in a small-scale randomized controlled trial in Cape Town, South Africa (n=60 families). The pilot study will use a mixed-methods approach to intervention evaluation. Self-report and observed quantitative data for intervention and control groups will be collected at pre-test and post-test evaluation. Primary outcomes will include parent-reports and observations of child behavior problems. In addition, as an exploratory study, this phase will examine initial pre-post intervention effects for potential mediating factors of parenting behavior, parental stress, parental depression, and perceived social support. However, this phase will not test mediation effects due to small sample sizes. Quantitative assessments will also collect data on program fidelity, exposure/adherence, participant engagement, and satisfaction. Furthermore, qualitative focus groups with intervention participants and group leaders will examine issues of program feasibility, content, deliver, and satisfaction. Randomization will be done on an individual level and include a wait-list control group that will receive the intervention 3 months after the post-test evaluation. Results from the feasibility pilot study will be shared with intervention partners and advisory groups. If necessary, final program adjustments will be made prior to further testing. Results will also be disseminated to community forums, local organizations, government stakeholders, and via academic conferences. Research hypotheses: Hypothesis 1: Children in the intervention group will demonstrate reduced observed and parent-reported child behavior problems in comparison to the control group. Hypothesis 2: Parents in the intervention group will demonstrate increased observed and self-reported positive parenting outcomes and decreased observed and self-reported harsh and inconsistent parenting outcomes in comparison to the control group. Hypothesis 3: Parents in the intervention group will demonstrate decreased parental depression and parental stress outcomes and increased perceived social support outcomes in comparison to the control group. Hypothesis 4: The Sinovuyo Caring Families Program will be implemented with an acceptable degree of program fidelity, exposure/adherence, and participant satisfaction.

NCT ID: NCT01683565 Completed - Preterm Birth Clinical Trials

Preemie Tots: A Pilot Study to Understand the Effects of Prematurity in Toddlerhood

Start date: September 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to examine whether supplementation with certain polyunsaturated fatty acids can help development and behavior of children born preterm.

NCT ID: NCT00912626 Completed - Child Behavior Clinical Trials

Family Functioning and Child Behavior When a Sibling is Critically Ill

Start date: June 2009
Phase: N/A
Study type: Interventional

The goal of this study is to determine if there is a correlation between an efficacious family environment and sibling behavior in families with children who are critically ill.

NCT ID: NCT00902395 Completed - Dental Caries Clinical Trials

Efficacy of Moderate Sedation for Dental Treatment of Young Children

Start date: June 2008
Phase: Phase 4
Study type: Interventional

There is lack of clinical trials on pediatric dental sedation. The purpose of this study is to test (using a randomized controlled trial design) the hypothesis that young children behavior during dental treatment improves with oral midazolam sedation. A further aim of this study was is explore whether behavior also changes over sessions needed to dental treatment completion.

NCT ID: NCT00133055 Completed - Child Behavior Clinical Trials

Parenting Matters: Helping Parents With Young Children

Start date: July 2005
Phase: Phase 2
Study type: Interventional

Sleep and discipline problems are the most common problems for parents of young children (ages 2 to 5 years old) and are the two concerns with the strongest relations to future child behavior problems. The Parenting Matters program combines treatment booklets and telephone support to help parents deal with sleep or discipline problems. Parents with concerns and who are interested in the study are identified during a visit to their family physician. We, the investigators at the University of Western Ontario, expect that parents receiving treatment booklets, along with usual care by their family physician, will have greater reductions in their child's sleep or discipline problems, improved parenting practices, and greater reductions in child behaviour problems after receiving the Parenting Matters intervention, compared to parents receiving usual medical care.

NCT ID: NCT00060697 Recruiting - Adolescent Behavior Clinical Trials

A Mother's Role in Delaying Onset of Sexual Activity in Her Children

Start date: December 2000
Phase: Phase 2
Study type: Interventional

The goal of this study is to enhance the mother's role in promoting avoidance of sexual risks and problem behaviors in 6- to 12-year-old children. Consenting mothers will attend a 10-session program designed to enhance the quality of mother-child communication, identify sexual risks, and increase parental monitoring and self-efficacy.

NCT ID: NCT00059241 Recruiting - Child Behavior Clinical Trials

The "Reach For Health" Program: Delaying Sexual Activity in Children

Start date: July 2000
Phase: Phase 2
Study type: Interventional

Working with multiple schools in Brooklyn, NY, this study will develop and evaluate school- and community-based strategies designed to reduce early sexual activity and risky sexual behavior in middle school-aged children. These strategies will focus on parent education, classroom health curriculum, and learning through participation in community service.