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Health Behavior clinical trials

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NCT ID: NCT03077568 Completed - Health Behavior Clinical Trials

Evaluation of a Web Application That Supports Behavior Change in Work Related Stress

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

A randomized controlled trial is needed to strengthen the evidence in the area of web-based self-management programs for stress-reduction. Aim The aim for the study is to compare the effects of the web-application that supports behavior change in stress-management to a waiting list group in persons with perceived stress. Method This study will have the design of a randomized controlled trial (RCT). The CONSORT guidelines will be used for reporting the study. Sample: Different sectors in the region will be included. Three different high-schools in Västerås City, social services authority in Västerås municipality, a large private company in the region, three different clinics within the county council and the municipality of Köping have signed the attestation of participation. Intervention: The intervention is the program for web-based stress self-management My Stress Control. Procedure: After informed consent the participants will, during approximately 2-4 months by their own go through the web-based program for stress self-management. The waiting-list group will also get access to My Stress Control after post-measurements. Data-analysis: Descriptive statistics will be used for demographic data. Missing data will be replaced as recommended for the different measurements included, commonly by using the mean for responded items within the sub scale. Inferential analyses will be conducted by using multivariate statistical analysis. Drop-out analysis will be conducted by comparing pre-interventions measures for those who completed the program with those who did not.

NCT ID: NCT03076996 Completed - Health Behavior Clinical Trials

Youth Power Action Feasibility Study of Online Support Group Intervention Among Adolescents Living With HIV in Nigeria

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

This study will examine the feasibility and acceptability of an intervention designed to improve retention in HIV care services and improve anti-retroviral therapy (ART) adherence among adolescents ages 15-19 years living with HIV enrolled in ART services.

NCT ID: NCT03071796 Completed - Health Behavior Clinical Trials

Influences of Multivitamin Supplementation on Health Parameters

Start date: March 7, 2017
Phase: N/A
Study type: Interventional

In this study the investigator will evaluate whether a liquid multivitamin supplement influences blood and vital parameters. Furthermore the investigator will establish the effects on life quality, mood and perception of stress and will characterize changes on immune system.

NCT ID: NCT03071029 Completed - Health Behavior Clinical Trials

PAFP Provider Feedback Trial in Nepal

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

A six-month RCT conducted within 36 health centres throughout urban and rural Nepal. The purpose of the RCT is to test the effectiveness of a peer comparison intervention at increasing uptake of long-acting reversible contraceptives (LARCs) as a percentage of PAFP uptake among clients who receive a safe abortion at a Marie Stopes International Nepal. The total sample size will be ~12,000 safe abortion clients. The primary outcome of interest is LARCs among safe abortion clients at Marie Stopes Centres in Nepal. The secondary outcome is to evaluate the impact of behaviorally designed intervention on the service providers' engagement in discussing measures to increase PAFP LARC uptake among women.

NCT ID: NCT03040154 Completed - Health Behavior Clinical Trials

Engaging Immigrants in Preventive Parenting Interventions

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

The objective of this community-based randomized controlled trial is to evaluate the outcomes of a theory-based parent engagement intervention (i.e., culturally-tailored video) aimed at promoting the participation of Filipino parents and grandparents in an evidence-based preventive parenting intervention.

NCT ID: NCT03036267 Completed - Health Behavior Clinical Trials

Feasibility of the BREATHE Asthma Intervention Trial

Start date: April 4, 2017
Phase: N/A
Study type: Interventional

Asthma rates are high and asthma control is greatly reduced in Black, Medicaid-insured adults, due in part to their poor adherence to inhaled corticosteroids (ICS), which in turn may be due to erroneous health beliefs about asthma and negative beliefs regarding ICS. A brief shared decision-making intervention for use by primary care providers in Federally Qualified Health Centers (FQHCs) has the potential to be a novel avenue to greatly improve asthma control in this high-risk patient group.

NCT ID: NCT03030534 Completed - Health Behavior Clinical Trials

Research Protocol On Developing an Integrated Technology-Moderated Institutional Health Promotion Model

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to adopt an operational research approach that seeks to design, develop and pilot-test the health-promotion lifestyle model that will enhance health-promoting behaviour and lifestyle modification of university staff in Nigeria. The following are the hypotheses of the study: 1. There will be a significant difference in the pre and post intervention practices of health promoting lifestyle behaviours (behaviour specific cognition and affect) of NOUN staff 2. There will be significant association between the health promoting lifestyle behaviours (behavioural outcome) and health status of NOUN staff 3. There will be a significant difference in the pre-and post-intervention health promoting lifestyle behaviours (behavioural outcome) of staff of NOUN 4. There will be a significant difference in the pre-and post-intervention health status measure (specific health measurement indicators) of staff of NOUN

NCT ID: NCT03021226 Completed - Health Behavior Clinical Trials

Evaluation of the Brothers United Fatherhood Program

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

The Brothers United Fatherhood Program (BUFP) will be conducting an evaluation that builds on literature and existing research from the healthy marriage/responsible fatherhood initiatives developed by ACF over the last 10 years, in particular the Supporting Healthy Marriage Program initiative that established a randomized clinical trial. The Brothers United Fatherhood Program will provide important data to expand the area of fatherhood development with the target population. This program is funded through an initiative of the Administration for Children and Families, Office of Family Assistance (OFA). The study is intended to measure if the identified interventions improve the well-being and relationship between targeted participants and their families. The study intends to focus on the following outcomes: - Demonstrate increased intake & knowledge of systems that help fathers - Improvement in knowledge of employment & learn new opportunities for economic mobility - Improvement communication & empathy skills towards partner - Increase in understanding of healthy marriage & its value to fathers - Demonstrate an understanding of financial planning - Demonstrate improved conflict resolution, behavior patterns, including those leading to domestic violence - Increase in reports of improved adult & child relationships - Demonstrate an increase job readiness skills such as employment preparedness & career direction

NCT ID: NCT03012516 Completed - Quality of Life Clinical Trials

Physical Activity on Prescription in Patients With Metabolic Risk Factors.

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

The aim of this study is to evaluate a one year intervention with physical activity on prescription (PAP) treatment for patients in a primary health care center setting versus an enhanced PAP-support with physiotherapist regarding physical activity (PA) level, metabolic health effects and health-related quality of life. One hundred ninety patients, 27-85 years, physically inactive, having at least one component of the metabolic syndrome and not responding with increased PA level after a 6-months PAP-treatment in primary health care centre are randomized to either enhanced support by physiotherapist (Intervention group) or continued ordinary PAP-treatment at the health care centre (Control group).

NCT ID: NCT03011385 Completed - Health Behavior Clinical Trials

Effects of Individual, Dyadic, and Collaborative Plans on Physical Activity in Partner-Partner Dyads

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

OBJECTIVE: The project aims at investigating of the effects of three types of planning (individual planning, collaborative planning, and dyadic planning) on physical activity among dyads.The influence of three planning interventions are compared with an active control condition, including physical activity education. PARTICIPANTS: The effects of the interventions are evaluated among dyads of two adults (partner-partner dyads). Adults forming dyads (e.g. two romantic partners, two relatives, two co-workers, two friends) who are in regular contact for at least one year will be enrolled. A minimum of 50 dyads enrolled into the each arm of the trial (a total of 200 dyads). The interventions consist of six planning sessions. DESIGN: The dyads are randomly assigned to one of four experimental conditions. The assessment of the main and secondary outcomes is conducted at the baseline, at 1 week after the first intervention session, at post-intervention (after six intervention sessions are completed), and at 6-, and 12-month follow-ups. OUTCOMES: Physical activity constitutes the main outcome, whereas health-related quality of life (HRQOL), body mass index, and sedentary behavior as well as the self-regulatory strategy called the use of planning (individual, dyadic and collaborative) are secondary outcomes.