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Self Efficacy clinical trials

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NCT ID: NCT03301714 Completed - Quality of Life Clinical Trials

Oral Health Education Interventions Among Seniors

Start date: October 15, 2017
Phase: N/A
Study type: Interventional

The study aims to assess the efficacy of an oral health education group based activity versus an individual based oral health education activity in terms of changes in oral health related quality of life (OHRQoL), self-efficacy and oral health knowledge.

NCT ID: NCT03281447 Completed - Quality of Life Clinical Trials

Nurse Navigation Versus Current Care Coordination During Colorectal Cancer Trajectories

NaviCan
Start date: February 26, 2016
Phase: N/A
Study type: Interventional

In western countries, the number of cancer survivors increases, and current cancer care seems insufficient with both patients' experiences of lack of help in transitions and up to 60 % of the patients having psychological problems after treatment. Further, Denmark shall have new hospitals, where researchers and healthcare professionals are expected to merge tasks and reach a higher patient experienced quality of care, without additional costs, so a better way to provide cancer care, which benefits the patients and supports the ideas within the new hospitals in Denmark, is needed. In a randomized controlled trial, the organizational structure of the healthcare system is challenged and the impact of a coherent nurse navigation practice compared to the currently existing department-specific care coordination is tested. The primary data are changes in patients' self-reported cancer-related self-efficacy from inclusion till one week after receipt of the information that they have reached the end of treatment, or in case of prolonged treatment, till not later than one year after inclusion. Patients can participate if they are 18 years of age or older, speak and understand Danish, and have a proven lesion suspected of cancer in the colon or rectum after colonoscopy or sigmoidoscopy at the Danish endoscopy centers at Odense University Hospital (the cities: Nyborg, Svendborg and Odense) or at Slagelse Hospital. Furthermore, participants must not be mentally retarded, they must not suffer from a constant life-threatening disease, and they must not suffer from, or be in the diagnostic phase of, dementia or severe psychiatric disease. Participants are allocated to support from nurse navigation or to current care coordination, and fill in four questionnaires during their cancer trajectory: 1) At inclusion, 2) Three days before treatment start, 3) One week after receipt of information about treatment end or not later than one year after inclusion, and 4) Six weeks after measure point 3. Data is analyzed using suitable statistical models. With positive results, participants in nurse navigation are better helped during their cancer trajectory and have a better psychological start on the rest of their lives after cancer treatment. Focus will be on colon and rectum cancer care, but the results will be transferable to similar settings. Furthermore, positive results will support changes in the onset of rehabilitation initiatives.

NCT ID: NCT03261700 Completed - Clinical trials for Intimate Partner Violence

Recovering From Intimate Partner Violence Through Strengths and Empowerment (RISE)

RISE
Start date: October 22, 2018
Phase: N/A
Study type: Interventional

Intimate partner violence (IPV) is a major health concern for women Veterans. IPV is associated with numerous physical and mental health conditions. VHA is implementing IPV screening programs to identify female patients who experience past-year IPV. Despite strong evidence that screening increases detection of IPV, less is established about how to intervene following IPV disclosure in health care settings, in order to improve health outcomes. Existing healthcare-based interventions result in minimal effects on health and well-being, likely because they are too brief and generic. In response, the PI has developed Recovering from IPV through Strengths and Empowerment (RISE), based on the IPV-related health care needs and preferences of women Veterans. RISE is designed to be delivered in primary care and is an individualized, variable-length, modular-based intervention that addresses - safety planning; - education on the health effects of IPV and warning signs; - increasing coping skills and self-care; - enhancing social support; - making difficult decisions; and - connecting with resources. This study is aimed at refining and evaluating RISE for use with female VA patients who have experienced past-year IPV. This brief counseling intervention is intended to be administered in conjunction with primary care, as this is a frequent point of healthcare contact for women Veterans and where disclosure of IPV is most prevalent.

NCT ID: NCT03124563 Completed - Sedentary Lifestyle Clinical Trials

Planning the Next Steps: Using an Implementation Intention Approach to Increase Daily Walking

Start date: June 2015
Phase: N/A
Study type: Interventional

The study goal is to design an intervention utilizing implementation intentions to help participants prospectively plan and visualize ways to increase activity for the next day among working adults who do not currently exercise or use an activity monitor. Investigators will assess the level of and changes in physical activity, and how this relates to various individual factors that are related to exercise and health, including self-efficacy, control beliefs, and cognition.

NCT ID: NCT03124537 Completed - Aging Clinical Trials

Increasing Physical Activity Among Sedentary Older Adults:What, Where, When, and With Whom

Start date: October 16, 2017
Phase: N/A
Study type: Interventional

The goal of this study is to develop a smart phone app to administer a behavior change program that helps adults to increase daily steps by planning where, when, and with whom to walk. The investigators tested the effectiveness of the walking program app for increasing the number of daily steps among sedentary older adults. The investigators examined the effects on self-efficacy and social integration/support.

NCT ID: NCT03019484 Completed - Self Efficacy Clinical Trials

Synergy, Self-efficacy, Breastfeeding and Care (SInergia, Autoeficacia, Lactancia y Cuidados)

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

The aim of the study was to evaluate the effectiveness of a breastfeeding self-efficacy promotion intervention. More specifically our objectives were to: explore changes in self-efficacy following the intervention; explore changes in the initiation and maintenance of breastfeeding following the intervention.

NCT ID: NCT02979990 Completed - Self Efficacy Clinical Trials

Learning From Online Video Education for Controlled Ovarian Stimulation

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

The Learning from Online Video Education (LOVE) study seeks to determine if online instructional videos on how to administer medication needed for in vitro fertilization (IVF) help improve the quality of life and reduce stress during the IVF process.

NCT ID: NCT02906306 Completed - Well-being Clinical Trials

Effects of Individual and Group Occupational Therapy on General Self-Efficacy, Psychological Well-Being, Personal Independence and Occupational Therapy in Older Adults

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

The objective of this study is to determine whether individual and/or group occupational therapy leads to changes in generalized self-efficacy and psychological well-being, and to identify the type of therapy that has the best effects on older adults.

NCT ID: NCT02770898 Completed - Self-efficacy Clinical Trials

Improving Family Holistic Health in Probationers

Start date: July 2015
Phase: N/A
Study type: Interventional

Evaluating the impact of probation on probationers is necessary for both effective practice of probation officers and their assessment of the success of their work. At present, there are limited studies that have evaluated the impact of probation services on probationers and their family. There are even fewer studies that have examined interventions on probationers' well-being and family relations in a Chinese society. Compared with the general population, probationers are associated with poorer mental (e.g., depression, lower levels of self-esteem, high level of stress) and physical health, and often experience higher levels of family conflict, and poorer quality of family relationships. Given the vulnerabilities, there is a need to strengthen and promote healthy lifestyle and enhance individual and family well-being among probationers. As part of the FAMILY project, the current study focuses on "FAMILY Holistic Health" which emphasizes a comprehensive approach to improving physical, mental, and social health and well-being. This project will be conducted as a pilot project in the Social Welfare Department (SWD) in the Eastern District of Hong Kong. Interventions will be delivered to promote and enhance probationer's wellbeing, as well as enhancing FAMILY 3Hs (Happiness, Health, and Harmony). Training programs will be provided to probation officers and/or workers of SWD in order to equip them with knowledge and skills in implementing health-related family intervention programs.

NCT ID: NCT02236455 Completed - Anxiety Clinical Trials

Effects of Complementary Therapies Delivered Via Mobile Technologies

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

The purpose of this study is to determine the effects of complementary therapies delivered via mobile technologies have a therapeutic effect on surgical patients' anxiety, pain, and self-efficacy in healing reports before, following, and at 10-day follow-up.