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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01260493
Other study ID # VårdkedjaVårdal
Secondary ID
Status Completed
Phase N/A
First received November 30, 2010
Last updated June 11, 2014
Start date October 2008
Est. completion date October 2011

Study information

Verified date June 2014
Source Vardalinstitutet The Swedish Institute for Health Sciences
Contact n/a
Is FDA regulated No
Health authority Sweden: Swedish National Council on Medical Ethics
Study type Interventional

Clinical Trial Summary

The present study "Continuum of care for frail elderly people" form part of the research programme "Support for frail elderly persons - from prevention to palliation" (www.vardalinstitutet.net) which comprises research into three interventions. The program comprises interventions addressing frail elderly people in different phases of the disablement process, from elderly people who are beginning to develop frailty to very frail elderly people receiving palliative care.

The intervention "Continuum of care for frail elderly people" addresses elderly people who are frail and that have a great risk of high health care consumption. The hypothesis is that an intervention program for frail elderly people can reduce the number of visits to the emergency department, increase the life satisfaction and maintain the functional ability. The intervention, including an early geriatric assessment at the emergency department, early family support, a case manager in the community with a multi-professional team and active follow-up by the case manager, contributes to early recognition of the elderly people's need of information, care and rehabilitation and of informal caregivers' need of information. It enhances the transfer of information and integrates the care between different caregivers and different care levels, thereby better recognize frail elderly people's needs. Specifically, this study is expected to show that the intervention has a positive effect on the frail elderly person's functional ability, life satisfaction, satisfaction with health and social care, and health care consumption.


Recruitment information / eligibility

Status Completed
Enrollment 181
Est. completion date October 2011
Est. primary completion date June 2010
Accepts healthy volunteers No
Gender Both
Age group 65 Years and older
Eligibility Inclusion Criteria:

- 80 years and older or 65 to 79 years and having at least one chronic disease and being dependent in at least one activity of daily living

Exclusion Criteria:

- acute severely sick who immediately needs the assessment of a physician (within ten minutes)

- those with diagnosis of dementia (or severe cognitive impairment)

- patients in palliative care

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Other:
integrated health care chain
Geriatric assessment at ED, case manager with multiprofessional team in the community, support for informal caregivers

Locations

Country Name City State
Sweden University of Gothenburg Gothenburg

Sponsors (2)

Lead Sponsor Collaborator
Vardalinstitutet The Swedish Institute for Health Sciences VinnVård

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Health Care Consumption Number of hospital days and admission will be analysed 1 year No
Primary Dependence in Activities of Daily Living Changes in number of person dependent in one or more daily activity from baseline to follow-up. 1 year No
Primary Satisfaction With Health and Social Care 1 year No
See also
  Status Clinical Trial Phase
Completed NCT02834728 - Frail Elderly Subjects - Evaluation and Follow-Up N/A