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Lifestyle clinical trials

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NCT ID: NCT02843269 Active, not recruiting - Neck Pain Clinical Trials

Multiple-component Workplace FRamed Intervention to Decrease Occupational Muscle Pain - FRIDOM

FRIDOM
Start date: September 2014
Phase: N/A
Study type: Interventional

Several RCT studies have aimed to reduce either musculoskeletal disorders, sickness presenteeism, sickness absenteeism or a combination of these among females with high physical work demands. These studies have provided evidence that workplace health promotion (WHP) interventions are effective, but long-term effects are still uncertain. These studies either lack to succeed in maintaining intervention effects or lack to document if effects are maintained past a one-year period. FRIDOM (FRamed Intervention to Decrease Occupational Muscle pain) is a WHP program among health care workers. A job group characterized by having high physical work demands, musculoskeletal disorders, high sickness presenteeism - and absenteeism. FRIDOM aimed to reduce neck and shoulder pain and secondary to reduce sickness presenteeism and sickness absenteeism. An other secondary aim was to decrease lifestyle-diseases such as other musculoskeletal disorders as well as metabolic-, and cardiovascular disorders - and to maintain participation to regular physical exercise training, after a one year intervention period. The entire concept was tailored to a population of female health care workers. This was done through a multi-component intervention including 1) intelligent physical exercise training (IPET), dietary advice and weight loss (DAW) and cognitive behavioural training (CBT).

NCT ID: NCT02786394 Completed - Aging Clinical Trials

Return to Everyday Activities in the Community and Home

REACH
Start date: May 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to test feasibility for the delivery and perceptions of a lifestyle model for middle-aged and older adults by involving participants in its development. The goal of the program is to reduce sedentary behaviour, increase physical activity, and increase strength and balance. An optional walking program will be run in parallel to emphasize the importance of moving more. Participants will be asked to fill out questionnaires on course delivery, content and effect throughout the program and 2-3 recorded interviews throughout the study. We will collect measurements of physical performance before and after the program.

NCT ID: NCT02744157 Completed - Quality of Life Clinical Trials

Long Term Effects of a Structured Lifestyle Program

Start date: January 2008
Phase: N/A
Study type: Interventional

The aim of the present study was to describe a structured intervention to reduce cardiovascular risk in a clinical setting and to study the effects of the program on lifestyle habits and quality of life in individuals at risk after six months and one year.

NCT ID: NCT02742662 Completed - Obesity Clinical Trials

Smart Technology for Weight Loss and Metabolic Health

Start date: April 2016
Phase: N/A
Study type: Interventional

The study will evaluate whether a technology-based lifestyle intervention program using primarily a smartphone platform is an acceptable and effective way for treating obesity. The goal of the program is to achieve weight loss and enhance the health of overweight or obese subjects by improving their diet and activity via smartphone applications as compared with conventional in-person weight management programs.

NCT ID: NCT02736214 Completed - Pregnancy Clinical Trials

Reproductive Life Plan-based Counseling With Men

Start date: October 2014
Phase: N/A
Study type: Interventional

Many women and men in fertile age are at risk for sexual transmitted infections and unwanted pregnancies, and have insufficient knowledge of health promoting lifestyle prior to conception. There is a need to increase awareness among people in fertile age about how sexual risk-taking and unhealthy lifestyle can negatively affect fertility and pregnancy outcomes. Previous studies on preconception health and care have mainly focused on women. The aim of our study was to investigate if Reproductive Life Plan-based counseling with a midwife could increase men's reproductive knowledge. The second aim was to evaluate men's experiences of the intervention.

NCT ID: NCT02669602 Enrolling by invitation - Chronic Disease Clinical Trials

Dynamic Mediterranean Prospective Cohort: the SUN Project

Start date: December 1999
Phase:
Study type: Observational

Dynamic prospective cohort of Spanish university graduates. The main objective is to evaluate the associations between nutrition and lifestyle and chronic diseases.

NCT ID: NCT02648555 Not yet recruiting - Lifestyle Clinical Trials

A Lifestyle Intervention to Improve in Vitro Fertilization Results

W+D
Start date: May 2016
Phase: N/A
Study type: Interventional

Embryo adhesion and placentation depend on tissue plasminogen activator (tPA)-mediated activation of brain-derived neurotrophic factor, vascular endothelial growth factor and other growth factors, formation of hemidesmosomes, and degradation of extracellular matrix and basement membrane, either directly or by activating matrix metalloproteinases. Since glucose and insulin stimulate release of a major tPA inhibitor by endothelial cells - plasminogen activator inhibitor (PAI)-1 - the investigators hypothesized that lifestyle interventions proven effective in maintaining glucose and insulin levels within the normal range would increase the take home baby rate in women undergoing assisted reproduction.

NCT ID: NCT02449460 Recruiting - Hypertension Clinical Trials

Cardiovascular Epidemiology in Russian Federation

ESSE-RF
Start date: July 2012
Phase: N/A
Study type: Observational

The study addresses epidemiology of cardiovascular risk factors and major cardiovascular diseases in Russian Federation (urban and rural population). 12 regions of 1600 participants in each will be included.

NCT ID: NCT02382250 Completed - Clinical trials for Coronary Artery Disease

Relationship Between Diet, Lifestyle, and the Severity of Coronary Artery Disease

Start date: February 1, 2015
Phase: N/A
Study type: Observational

This study is a prospective study of patients referred for coronary angiography at Bellevue Hospital Center and NYU Langone Medical Center. Subjects enrolled in this study will complete two one-page questionnaires, including information about diet, lifestyle, perceptions of health and perceived barriers to healthy lifestyles. Patients will be contacted at one and six months following their procedure to complete follow-up questionnaires to assess changes in diet and perceptions of their health after knowing the results of their coronary angiogram. The primary outcome measure will be change in dietary patterns/perception of lifestyle between baseline and one- month and six-month follow-up. Secondary measures will include association between dietary patterns/perception of lifestyle and degree of CAD and socioeconomic status.

NCT ID: NCT02211781 Completed - Lifestyle Clinical Trials

Study of Diets and Way of Life of Native Americans and Hispanics in New Mexico During the Time of the Trinity Nuclear Test

Start date: August 1, 2014
Phase:
Study type: Observational

Background: - The National Cancer Institute has been studying health risks to people in New Mexico at the time of the first nuclear bomb test. This was called the Trinity nuclear test. It took place in 1945. Researchers want to also learn about Native Americans and Hispanics at that time. They want to learn about their way of life and their diets. This will give a more complete picture of the health risks to people in New Mexico in 1945. Objectives: - To learn about the activities and eating habits of Hispanic and tribal communities during the 1940s. - To see if a group of Hispanic and Native Americans who were living in New Mexico in 1945 can be gathered. Eligibility: - Native American or Hispanic adults who were alive in 1945. They must know firsthand about the lifestyle and diet in New Mexico at that time. Design: - Participants will have 1 visit. They will be interviewed at a place like a library or office. They will answer questions about their lifestyle and diet around 1945. This will take up 60 90 minutes. - Participants may agree to have their interviews taped. Their names will not be kept with their answers from the interviews.