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Self Efficacy clinical trials

View clinical trials related to Self Efficacy.

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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: NCT02830386 Recruiting - Self Efficacy Clinical Trials

Chinese Registry of Assisted Embolization for Ruptured Wide Necked Intracranial Aneurysm Using LVIS Stent

CRANIAL-2
Start date: June 2016
Phase: N/A
Study type: Observational

This study aims to investigating the efficacy and safety of low profile visualized intraluminal support (LVIS) stents for the treatment of ruptured intracranial saccular aneurysms. The follow-up duration is 1 year.

NCT ID: NCT02830373 Recruiting - Self Efficacy Clinical Trials

Chinese Registry of Assisted Embolization for Unruptured Wide Necked Intracranial Aneurysm Using LVIS Stent

CRANIAL-1
Start date: June 2016
Phase: N/A
Study type: Observational

This study aims to investigating the efficacy and safety of low profile visualized intraluminal support (LVIS) stents for the treatment of unruptured intracranial saccular aneurysms.

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: NCT02391766 Enrolling by invitation - Quality of Life Clinical Trials

Group Intervention Empowerment Dementia

Start date: September 2014
Phase: Phase 0
Study type: Interventional

After diagnosis of a dementing illness, patients and their spouses have many concerns related to the disease and their future. This often leads to poor psychological well-being and reduced health-related quality of life (HRQoL) of the family. Support for Empowerment has been proven to be an effective method to improve prognosis of asthma, heart failure, osteoarthritis.and diabetes. However empowering interventions have not been studied in dementia. Therefore, the investigators aim was to examine, in an objective-oriented group intervention, the efficacy of empowerment support program (ESP) on the HRQoL of dementia patients and their spousal caregivers as well as on the sense of competence and psychological well-being of caregivers. Methods: During the years 2014 to 15, 180 dementia patients and their spouses will be recruited from memory clinics or day centers and randomized into two arms: 90 patients for group-based ESP sessions including topics selected by the participants and the use of the by us for us guides, 90 patients will serve as controls in usual community care. Sessions may include topics on dementia, active lifestyle and prevention for cognitive decline, spousal relationship, future planning and emotional well-being. The patients and spouses will have their separate group sessions (ten participants per group) once a week for eight weeks.