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The ElderCare Project
This study is currently recruiting participants.
Verified by Memorial University of Newfoundland, September 2007
First Received: March 26, 2007   Last Updated: September 20, 2007   History of Changes
Sponsored by: Memorial University of Newfoundland
Information provided by: Memorial University of Newfoundland
ClinicalTrials.gov Identifier: NCT00452465
  Purpose

Hypothesis: It is hypothesized that older adults who receive the ElderCare intervention will, when compared with a control group of older adults show a significant improvement in quality of life,a significant decrease in symptomatology, significantly higher satisfaction with their care, and less utilization of health care resources.

The Eldercare project involves a detailed assessment by a nurse done in the patients home, followed by the development and delivery of a Eldercare Plan using a Goal Attainment Scaling approach.

Outcomes include quality of life, symptomatology, satisfaction, and health care utilization.


Condition Intervention
Care of the Elderly
Behavioral: ElderCare Plan

Study Type: Interventional
Study Design: Health Services Research, Randomized, Open Label, Active Control, Parallel Assignment
Official Title: The elderCare Project: Primary Healthcare for Community Living Old Elderly

Further study details as provided by Memorial University of Newfoundland:

Primary Outcome Measures:
  • Quality of Life [ Time Frame: Prospective ]
  • Symptomology [ Time Frame: Prospectiv e ]
  • Satisfaction [ Time Frame: Prospective ]
  • Health care service utilization [ Time Frame: Prospective ]

Estimated Enrollment: 320
Study Start Date: February 2007
Estimated Study Completion Date: March 2010
Detailed Description:

Objectives: The main objective of this study is to improve the care of the old elderly. This will be done by implementing and evaluating a year long program which is intended to optimize quality of life, symptom management and utilization of both health care and community services for the old elderly.

Hypothesis: It is hypothesized that older adults who receive the ElderCare intervention will, when compared with a control group of older adults: a) show a significant improvement in quality of life - as measured by the SF-36, b) show a significant decrease in symptomatology - as measured by the Comorbidity Symptom Scale, c) show significantly higher satisfaction - as measured by the Patient Satisfaction Questionnaire d) have increased utilization of community-based services, e) have fewer emergency room visits, f) have fewer hospitalizations, and g) fewer visits to the family doctor

Research Plan: The ElderCare program is a nurse-based program of home-delivered care that will be linked directly with the primary care practitioner or primary care team of each older adult in the study. The nurse will be part of the primary health care team for a number of different family physicians practices. The nurse will serve as a link or interface between the family physicians practice (or other primary health care professional or team) and the community services. The nurse will i) evaluate the clinical and personal needs of the patient, ii) develop a management plan based on that review (the review includes chart review, patient assessment and contacting community agencies that have been involved with the patients care). , iii)review the plan with the family physician and the patient/family; iv) implement the plan v) provide patient education; and vi) monitor the patient regularly in his/her home over the course of a year. Evaluation will involve comparing a group of old elderly who receive the ElderCare program (intervention) with a control group. Groups will be evaluated using a variety of assessments which will be done at baseline, 6 months and 12 months.

The steps that will be taken in carrying out the research are outlined as follows:

  1. Physician Recruitment
  2. Patient Recruitment
  3. Baseline Data Collection
  4. Randomization - Physicians will be cluster randomized to decrease contamination
  5. ElderCare Program delivered to intervention group old elderly
  6. Usual care for control group old elderly
  7. Outcomes measured at 6 and twelve months - outcomes include quality of life, change in symptomatology, patient satisfaction, use of community services, visits to family doctor, hospitalizations, emergency room visits
  8. Data Analysis, Interpretation, Reporting and Analysis
  Eligibility

Ages Eligible for Study:   80 Years and older
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Patients of a family practice who are 80 years or older, who are independently living and do not have a diagnosis of dementia.

Exclusion Criteria:

  • MMSE score 25 or less
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00452465

Contacts
Contact: Marshall Godwin, MD 709-777-8373 godwinm@mun.ca
Contact: Farah McCrate, MSc 709-777-6694 fmccrate@mun.ca

Locations
Canada, Newfoundland and Labrador
Primary Healthcare Research Unit, Memorial University of Newfoundland Recruiting
St. John's, Newfoundland and Labrador, Canada, A1B 3V6
Contact: Farah McCrate, MSc     709-777-6694     fmccrate@mun.ca    
Contact: Marshall Godwin, MD     709-777-8373     godwinm@mun.ca    
Sponsors and Collaborators
Memorial University of Newfoundland
Investigators
Principal Investigator: Marshall Godwin, MD Memorial University of Newfoundland
  More Information

No publications provided

Study ID Numbers: 200603MOP-158331-SDA-CJAA
Study First Received: March 26, 2007
Last Updated: September 20, 2007
ClinicalTrials.gov Identifier: NCT00452465     History of Changes
Health Authority: Canada: Research Ethics Board

Keywords provided by Memorial University of Newfoundland:
Elderly
Nursing care plan
Quality of Life

Study placed in the following topic categories:
Quality of Life

ClinicalTrials.gov processed this record on September 10, 2009