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Risk Reduction Behavior clinical trials

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NCT ID: NCT01170260 Completed - Health Behavior Clinical Trials

Alcohol, Marijuana, and Risky Sex: Group Interventions With Detained Adolescents

MARS
Start date: August 2010
Phase: N/A
Study type: Interventional

This research is studying behaviors that young people engage in that may place them at risk for contracting a sexually transmitted disease like HIV/AIDS, and what kind of educational program works best to reduce these risky behaviors.

NCT ID: NCT00906321 Completed - Clinical trials for Risk Reduction Behavior

Facilitating Web-based Patient Decision Support: Decision About Medication to Lower Breast Cancer Risk

Start date: May 18, 2009
Phase: N/A
Study type: Interventional

Background: - Chemoprevention is the use of preventive medications to reduce the risk of breast cancer for women who are at a high risk of developing the disease. Although the treatment has shown effectiveness in preventing cancer development, chemoprevention is notably underutilized even by women who are at a high risk of developing breast cancer. - Researchers are interested in determining if better decision support mechanisms, such as interactive Web sites, can help to overcome some of the barriers to chemoprevention. Objectives: - To develop and test a prototype Web-based module that will provide decision support to women who are considering chemoprevention for breast cancer. Eligibility: - Women 35 years of age and older who are at high risk for breast cancer and whose doctor has recommended chemoprevention (either Tamoxifen or Raloxifene), and who have no other history of cancer (apart from non-melanoma skin cancer or precancerous cervical lesions). - Participants must have a working e-mail address and access to a computer with internet access and a telephone. Design: - Participants who are considering chemoprevention will be randomized to a Web-based decision support module or standard care online information resources. - Participation lasts two months and involves using the online resources provided and filling out questionnaires two times during the study (at the beginning and the end). The first time will be at the begin of the study. - No medical treatments are offered as a part of this study

NCT ID: NCT00443638 Completed - Clinical trials for Risk Reduction Behavior

Longitudinal Follow Up of Subjects Enrolled in Randomized Trial of Prenatal and Infancy Home Visitation

ElmiraY19
Start date: May 1998
Phase: N/A
Study type: Interventional

The Elmira follow-up study is designed to assess the extent to which prenatal and infancy home visitation by nurses affects the life-course development of 19-year-old youth whose mothers received those services during pregnancy and the first two years of the child's life.

NCT ID: NCT00438594 Completed - Clinical trials for Risk Reduction Behavior

Age 9 Follow-up of Preventive Intervention (Denver)

DenverY09
Start date: February 2004
Phase: N/A
Study type: Interventional

To examine the impact of prenatal and infancy home visiting by paraprofessionals and by nurses from child age 2 through 9.

NCT ID: NCT00438516 Completed - Clinical trials for Adolescent Development

Follow-up of Families in Early Preventive Intervention

MemphisYear9
Start date: June 2000
Phase: N/A
Study type: Interventional

This project supports the post-third-grade assessment of 693 children and their families who were enrolled in a randomized trial of a program of prenatal and infancy home visitation by nurses that was epidemiologically and theoretically grounded. The project will determine whether the beneficial effects of the program on maternal, child, and family functioning extend through the early elementary school years, giving particular attention to maternal life-course and children's emerging antisocial behavior. Assessments of the children will be based on both mother and teacher reports. Teachers are independent, natural raters of the children's adaptation to an important social context. There are numerous reasons to expect that, from a developmental perspective, the effects of the program will increase as children experience the increased academic demands associated with entry into third grade. In addressing these questions, the current study will determine the extent to which this program of prenatal and infancy home visitation by nurses can produce enduring effects on maternal and child functioning (giving particular attention to the prevention of early-onset disruptive behavior disorders) in urban African Americans that are consistent with those achieved with whites in a central New York state county in a separate trial of this program conducted over the past 20 years.

NCT ID: NCT00438282 Completed - Clinical trials for Risk Reduction Behavior

Age 6 Test of Home Visits by Nurses vs Paraprofessionals

DenverY06
Start date: March 2001
Phase: N/A
Study type: Interventional

To examine the impact of prenatal and infancy home visiting by paraprofessionals and by nurses from child age 2 through 6.

NCT ID: NCT00438165 Completed - Clinical trials for Risk Reduction Behavior

Age 12 Follow-up of Early Preventive Intervention (Memphis)

MemphisY12
Start date: September 2003
Phase: N/A
Study type: Interventional

To examine the impact of prenatal and infancy home visiting by nurses from child age 2 through 12.

NCT ID: NCT00153426 Completed - Clinical trials for Risk Reduction Behavior

West Virginia WISEWOMAN Project

Start date: July 2003
Phase: N/A
Study type: Interventional

To provide low-income, under- or uninsured 40- to 64-year-old women with the knowledge, skills, and opportunities to improve diet, physical activity, and other lifestyle behaviors to prevent, delay and control cardiovascular and other chronic diseases.