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Health 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: NCT02056483 Completed - Depression Clinical Trials

REBECCA - Research in Rehabilitation After Breast Cancer

REBECCA
Start date: July 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to examine if a psychosocial intervention including a nurse navigator and systematic symptom screening may reduce psychological and physical symptoms as well as health behavior after breast cancer.

NCT ID: NCT02053194 Completed - Health Behavior Clinical Trials

A Trial to De-prescribe Inappropriate Medications in the Community Dwelling Elderly

D-PRESCRIBE
Start date: March 2014
Phase: Phase 4
Study type: Interventional

The objective of this trial is to test the beneficial effect of a pharmacist-initiated knowledge transfer intervention to both patients and prescribers on the discontinuation of inappropriate prescriptions, compared to usual care. The investigators hypothesize that the pharmacist-led intervention will reduce inappropriate prescriptions by at least 20% over 6-months compared to usual care. The intervention consists of simultaneously educating consumers and providing physicians with an evidence-based pharmaceutical opinion on inappropriate prescriptions.

NCT ID: NCT02012712 Completed - Health Behavior Clinical Trials

Personal Health Records and Elder Medication Use Quality

Start date: July 2010
Phase: N/A
Study type: Interventional

Purpose: To examine the impact of a personal health record (PHR) on medication use safety among older adults. Background: Online PHRs have potential as tools to manage health information. We know little about how to make PHRs accessible for older adults and what effects this will have. Methods: A PHR was designed and pretested with older adults and tested in a six-month randomized controlled trial. After completing mailed baseline questionnaires, eligible computer users aged 65 and over were randomized 3:1 to be given access to a PHR (n=802) or serve as a standard care control group (n=273). Follow-up questionnaires measured change from baseline medication use, medication reconciliation behaviors, and medication management problems.

NCT ID: NCT01979107 Completed - Smoking Clinical Trials

Early Detection of and Intervention Towards Chronic Diseases Among Individuals Without Formal Education

Start date: April 22, 2014
Phase: N/A
Study type: Interventional

In this randomized controlled study it is investigated if a proactive action by the general practitioner offering individuals without formal education a preventive health check will lead to a larger number of diagnoses in form of chronic obstructive pulmonary disease, cardiovascular diseases, and diabetes among participants in the intervention group compared to the control group. Furthermore it will be investigated if the proactive action by the general practitioner will be associated with a higher smoking cessation rate at 12 month follow-up.

NCT ID: NCT01969864 Completed - Health Behavior Clinical Trials

University Student Intervention to Increase Organ Donation

Start date: October 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of brief organ donation video interventions on consent for organ donation among college and university students. Our hypothesis is that the organ donation video interventions will be superior to lay health websites for increasing organ donation consent.

NCT ID: NCT01963494 Completed - Physical Activity Clinical Trials

Days in Motion: A Planning Intervention Study With Couples to Enhance Daily Physical Activity

DiM
Start date: March 2013
Phase: N/A
Study type: Interventional

Regular physical activity is one prominent health-protective behaviour which might increase with the help of self-regulatory strategies such as action planning. The aim of this randomised controlled trial is to examine changes in daily moderate physical activity in couples following (a) a dyadic planning intervention, (b) an individual planning intervention or (c) a no-planning control condition. Changes in daily physical activity will be examined over a period of one year. It is assumed that target persons from couples receiving a dyadic planning intervention will show greater increases in daily physical activity than target persons from couples receiving an individual planning intervention. For couples receiving a dyadic planning intervention or an individual planning intervention, it is hypothesized that target persons will show higher increases in daily physical activity than target persons from couples participating in the no-planning control condition.

NCT ID: NCT01943734 Completed - Health Behavior Clinical Trials

The Influence of Health Information in Stretch Break Program Participant's Lifestyle

Start date: March 2010
Phase: N/A
Study type: Interventional

Objective: To verify the influence of information passed during anthropometric assessment would have in physical exercise (PhE) and eating habits of 14 participants (female=11; 51,07+-8,17 years) from the Stretch Break Program of Federal University of Paraíba (SBP of FUPb). Methods: The research was a descriptive cross-sectional quantitative and qualitative approach. Were applied, between March and May of 2010, anthropometric evaluation and semi-structured interviews. During the evaluation were provided information and guidance on health.

NCT ID: NCT01878214 Completed - Cancer Clinical Trials

Promoting Smoking Cessation in Carpenters

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

The purpose of this study is to test an innovative and sustainable intervention to increase participation in a union-sponsored smoking cessation program among carpenters and floor layers. The investigators will conduct a randomized controlled trial comparing targeted messaging versus standard messaging. All subjects will receive information about the free, union-sponsored smoking cessation program. Subjects randomized to the intervention group will receive additional targeted materials to encourage enrollment in the union's smoking cessation program. The intervention will include monthly mailed and text messages. The investigators hypothesize that subjects who receive targeted messages will be more likely to enroll in the union-sponsored smoking cessation program, be more likely to show change in readiness to quit smoking, and be more likely to quit smoking compared to subjects who receive only standard messaging.

NCT ID: NCT01875146 Completed - Health Behavior Clinical Trials

Effects of High-intensity Interval Training in Combination With Side-alternating Whole-body Vibration

Start date: January 2013
Phase: N/A
Study type: Interventional

Investigation of the training effects following 8 weeks of high-intensity interval training (HIT)in combination with side-alternating whole-body vibration compared to conventional HIT or side-alternating whole-body vibration. The adaptations are investigated on a molecular (muscle biopsy of the M. vastus lateralis) and systemic (e.g. cycling, jumping mechanography, dynamometry) level. In addition, the acute effects of the first and last training session will be investigated on a molecular (e.g. satellite cell activation, mRNA abundance) and systemic (e.g. ventilatory ga exchange, heart rate, rating of perceived exertion) level.