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Hospitalization clinical trials

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NCT ID: NCT00828217 Recruiting - Hospitalization Clinical Trials

Adapted Physical Activity, Health-related Quality of Life and Satisfaction With Care in Hospitalized Children

ACTIVHOP
Start date: November 2008
Phase: N/A
Study type: Interventional

The aim of this study is to assess the efficacy of adapted physical activity intervention on health-related quality of life and satisfaction with care in hospitalized children and adolescents. This is a randomized controlled study. The hypothesis is that children practicing adapted physical activity during their hospitalization present a higher health-related quality of life and satisfaction with care than those who do not.

NCT ID: NCT00715962 Completed - Hospitalization Clinical Trials

Efficacy and Safety of a Hospital Walking Program for Older Adults

Start date: January 2010
Phase: Phase 2
Study type: Interventional

Low mobility, defined as being limited to bed or chair, is common during acute hospitalization. This study will evaluate the impact and safety of a hospital walking program for older patients during acute general medical hospitalization. Participants who are 65 years of age or older, will be randomized to usual care (UC) or to a hospital walking program (WP), which includes twice daily walks with assistance, provision of necessary ambulatory devices, and a behavioral intervention strategy designed to encourage out of bed activity. Throughout hospitalization, the WP and UC veterans will were wireless monitors on the thigh and ankle that measure activity. The primary goal will be in increase the length of time veterans spend out of bed and to assure this out of bed activity is safe.

NCT ID: NCT00527774 Completed - Quality of Life Clinical Trials

Effect of HCV Infection on Insulin Resistance and Malnutrition-inflammation Complex Syndrome in Regular Hemodialysis Patients

Start date: September 2007
Phase: N/A
Study type: Observational

The purpose of this study is to study whether hepatitis C virus (HCV)infected maintenance hemodialysis (MHD)patients have distinct metabolic, inflammatory and adipokine characteristics that can be linked to poor clinical outcome and to examine the hypothesis that HCV infected MHD patients with metabolic syndrome have higher risks for hospitalization, cardiovascular and all-cause mortality.

NCT ID: NCT00501501 Completed - Hospitalization Clinical Trials

The Association Between Delivery Method and Maternal Rehospitalization

Start date: January 1999
Phase: N/A
Study type: Observational

Hypothesis: The rates of rehospitalization after cesarean section are significantly higher than those following spontaneous vaginal delivery and are due mainly to late bleeding and less to infection.

NCT ID: NCT00462059 Completed - Hospitalization Clinical Trials

Assessment of a Medication Reconciliation Program on Transitional Care

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

The purpose of this study is to assess and compare the effectiveness of the Kaiser Permanente Colorado’s (KPCO) Call Center’s Medication Reconciliation Program and standard care in regards to their impacts on emergency department (ED) and urgent care visits, inpatient rehospitalizations, and adherence to preferred, formulary medications.

NCT ID: NCT00370916 Completed - Hospitalization Clinical Trials

Reducing Transition Drug Risk

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

Patient transfer between sites of care is regular practice during an episode of care in our current health care system. Yet inter-site transfer is associated with lapses in care quality that adversely affect patient outcomes. A common iatrogenic harm precipitated at the time of transfer is harm from drug prescribing, or adverse drug events (ADEs). In this study we will evaluate a medication reconciliation tool developed to help providers make effective prescribing decisions at the time of transfer between VA sites of care (Improved Prescribing after Transfer (IPT)). We will evaluate the quantitative effectiveness of the tool in reducing transition drug risk and ADEs. We additionally will conduct focus group discussions and cognitive task analysis among end-users to better understand how providers make drug-prescribing decisions at the time of transfer and to assess factors influencing effective use of the tool.

NCT ID: NCT00278746 Completed - Diarrhea Clinical Trials

Addition of Zinc to the Current Case Management Package of Diarrhea in a Primary Health Care Setting

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

Several studies have shown the beneficial effect of zinc treatment in acute diarrhea. There was a significant reduction in duration of the treated episodes and in their severity as measured by diarrheal stool output or frequency. Zinc is a potentially important immunomodulator or nutraceutical which may have great impact as therapeutic agent in conditions like diarrhea and pneumonia. The issue is whether and how zinc should be introduced in primary health care programs for treatment of acute diarrhea. A practical, sustainable intervention for introduction of zinc as treatment of acute diarrhoea in national programs is therefore required. This study aimed to address this issue.

NCT ID: NCT00278681 Completed - Diarrhea Clinical Trials

Effectiveness of Adding Zinc to the Current Case Management Package of Diarrhea in a Primary Health Care Setting

Start date: August 2003
Phase: Phase 1
Study type: Interventional

Use of zinc in diarrhea may be an effective intervention to reduce hospitalizations and child mortality as it could reach the most vulnerable children in a community and reduce severity of not only diarrhea but also of associated infections. It might also potentially reduce antibiotic use. We conducted a pilot study prior to conducting a community based controlled effectiveness trial to assess whether addition of zinc as a therapeutic modality for diarrhea delivered through existing channels, reduces visits to health care providers, antibiotic and other drug use, and increases ORS use during diarrhea.

NCT ID: NCT00244673 Completed - Mortality Clinical Trials

Randomized Study of Not Giving Diphteria-tetanus-pertussis Vaccination With or After Measles Vaccination

Start date: October 2005
Phase: Phase 4
Study type: Interventional

In non-randomized studies, routine childhood vaccinations have been observed to have non-targeted effects. Difteria-tetanus-pertussis (DTP) vaccine provided with or after measles vaccine (MV) is associated with increased mortality in areas with herd immunity to pertussis. We will examine in a randomised study of 6000 children the effect of not administering DTP simultaneously with or after MV on overall child mortality, hospitalization rates, and the immunological responses after vaccination. We will also examine potential sex-differential effects in the outcomes and interactions with other vaccines, other health interventions and season.