NCT00316966

Brief Summary

With the introduction of the National Insurance Law in Israel in 1995, there have been increased efforts to reduce hospitalization in general and length of stay in the hospital in particular. Under nourished patients have been shown to have a longer mean length of stay and they are more likely to suffer from complications, which significantly increase cost of care. Intense nutritional intervention programs, aimed at decreasing rehospitalizations and post hospitalization complications, are not clearly currently included in the basket of services provided under the law. Nutritional intervention has been shown to be clinically efficacious and cost-effective. Demonstration of the benefits of such intervention, both in terms of reduced expenditures and quality of care, may open a path for specific nutritional intervention programs that are needed for older persons during and after discharge from Acute Care. Given the effort made to reduce the length of hospitalization time, even in frail elderly patients, it is clear that full scale nutritional intervention cannot be completed during their hospitalization. Therefore, there is a need to create continuity between in-patient and follow-up nutritional intervention. This combined policy has the potential to improve general health, reduce the rates of under nutrition and its associated complications, and thus reduce future hospitalization, along with the mortality and morbidity associated. It is plausible that improved general health and less frequent hospitalization will eventuate in cost reduction and allow the intervention to be cost effective. Furthermore, the descriptive information regarding the nutritional status of older patients admitted to an Acute Care department may be important for policy makers in their development of nutritional intervention programs to support the elderly before, during and after hospitalization. Study Hypothesis: We hypothesize that multidisciplinary nutritional intervention, during and following hospitalization, will improve dietary intake and nutritional status. Improvement in nutritional status will, in turn, cut health care costs by decreasing the use of health services. In-hospital nutritional care will be beneficial, but combined in-hospital and community care will be more clinically efficacious and more cost effective in the long run.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P75+ for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2003

Completed
2.9 years until next milestone

First Submitted

Initial submission to the registry

April 20, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

April 21, 2006

Completed
Last Updated

August 10, 2010

Status Verified

May 1, 2005

First QC Date

April 20, 2006

Last Update Submit

August 9, 2010

Conditions

Keywords

Nutritional status, dietary intervention, health care use, costs

Outcome Measures

Primary Outcomes (2)

  • Health care use

  • Nutritional status

Secondary Outcomes (2)

  • Dietary intake

  • Blood measurements

Interventions

Eligibility Criteria

Age65 Years - 95 Years
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • \- All patients aged 65 or over admitted to one of three Internal Medicine Departments (A, C, F) at Soroka hospital during 18 months will be recruited

You may not qualify if:

  • Having cancer, having cognitive function \< 24, being clinically depressed and inability or unwillingness to sign an informed consent. In addition, due to the need for long-term intervention, only patients who live in the city of Beer-Sheva will be included. -

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ben-Gurion University

Beersheba, 84105, Israel

Location

Study Officials

  • Danit R Shahar, PhD

    Ben-Gurion University, Beer-Sheva, Israel

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
FACTORIAL
Sponsor Type
OTHER

Study Record Dates

First Submitted

April 20, 2006

First Posted

April 21, 2006

Study Start

June 1, 2003

Last Updated

August 10, 2010

Record last verified: 2005-05

Locations