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Self Efficacy clinical trials

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NCT ID: NCT01385241 Completed - Clinical trials for Human Immunodeficiency Virus (HIV)

Feasibility of a Stigma Reduction Intervention for Human Immunodeficiency Virus (HIV)-Infected Women

Start date: July 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to test the feasibility of a stigma reduction intervention in Human Immunodeficiency Virus(HIV)-positive women using a video of first-person narratives delivered via personal Ipod Touch.

NCT ID: NCT01327729 Recruiting - Hepatitis C Clinical Trials

Y- Shaped Pegylated Interferon (YPEG-IFNα-2a) Plus Ribavirin in Egyptian Patients With Untreated Chronic Hepatitis C

Start date: November 2010
Phase: Phase 2/Phase 3
Study type: Interventional

The objective is to assess the efficacy, dosing, safety and tolerance of Y- shaped pegylated interferon (YPEG-IFNα-2a) plus ribavirin in Egyptian patients with chronic hepatitis C and with no prior treatment for hepatitis C virus (HCV). Methods: Randomized, Open-label trial, in 3 parallel groups (each of 100 patients)

NCT ID: NCT01179854 Completed - Self Efficacy Clinical Trials

Remegal Different Doses in Patients With Refractory Partial Seizures

Start date: September 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine weather different doses of Remegal are effective,safety and tolerant in Additional Therapy for Patients With Refractory Partial Seizures and pharmacokinetics definition

NCT ID: NCT01141556 Completed - Self Efficacy Clinical Trials

Effects of High-dose Intravenous Selenium (Selenase®) in Adult Patients Subjected to Elective All-cause Heart Surgery

Start date: December 2010
Phase: Phase 3
Study type: Interventional

Selenoenzymes play a major role in protecting cells against lipid peroxidation and they are involved in the inflammatory response regulation. The degree of selenium deficiency correlates with disease severity and the incidence of mortality in critically ill patients. The aim of our study is to evaluate, if high dosis selenium supplementation (loading dose 4000 μg, daily dosage 1000 μg) results in a significant reduction of inflammation-induced organ dysfunction and length of ICU-stay in patients after heart surgery.

NCT ID: NCT01001286 Completed - Education Clinical Trials

Questscope Non-Formal Education Impact Study

QSNFEIS
Start date: October 2009
Phase: Phase 2
Study type: Interventional

This randomized controlled trial (RCT) evaluates the effectiveness of Questscope Non-Formal Education (QS NFE) on impacting psychosocial outcomes for out-of-school youth, ages 13-21, in Jordan. QS NFE is an empowerment-based education program. A unique agreement with the Jordanian Ministry of Education enables participating youth to receive a 10th-grade equivalent certificate upon successful completion of the 24-month non-formal education. The main components of QS NFE include retraining formal education teachers for fostering positive relationships with at-risk youth, asset-building learning and social activities, and a youth-driven learning environment. The study hypothesis is that by engaging youth in positive relationships with local teachers and enabling the youth to drive the learning experience, the intervention will have positive impacts on general self-efficacy, social supports, social skills, and strengths and difficulties.

NCT ID: NCT00888953 Completed - Quality of Life Clinical Trials

Nursing Homes Study of Fall Risk Assessment Oriented to Intervention

EMERCOIR
Start date: May 2009
Phase: N/A
Study type: Interventional

The aim of the study is to establish the impact of a falls screening questionnaire in the adoption of preventive interventions and eventually in the reduction of falls and its consequences in elder people living in nursing homes.

NCT ID: NCT00512590 Completed - Pain Clinical Trials

Pilot Study: Relaxation and Guided Imagery in Hispanic Persons Diagnosed With Fibromyalgia

Start date: April 2005
Phase: N/A
Study type: Interventional

The purpose of this pilot study was to test the effects of a 10-week relaxation and guided imagery intervention on pain perception, functional status, self-efficacy and levels of distress in Hispanic adults diagnosed with fibromyalgia.

NCT ID: NCT00145834 Completed - Breastfeeding Clinical Trials

Early Breastfeeding Cessation - is It Possible to Prevent?

Start date: February 2004
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate if a postnatal public health breastfeeding intervention relying on the importance of the psychosocial factors can prolong the period with exclusive breastfeeding duration among mothers who want to breastfeed.