Skip to main content
Clinical Trials/NCT02273934
NCT02273934
Unknown
Not Applicable

The Effectiveness of Reablement in Home Dwelling Adults. A Quasi Experimental Trial

Frode F. Jacobsen1 site in 1 country500 target enrollmentApril 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Physical Disability
Sponsor
Frode F. Jacobsen
Enrollment
500
Locations
1
Primary Endpoint
Change in score in Canadian Occupational Performance Measure
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to determine whether a special kind of rehabilitation offered to home-dwelling adults is effective with regards to functional ability, health-related quality of life, coping, mental health and municipal costs.

Detailed Description

Health promotion and prevention of functional decline among home dwelling adults and immediate onset of rehabilitation, can improve function, and reduce or delay need for home-based assistance and institution placement. In the coming years there will be a significant increase in number of persons in Norway that need interventions aiming at coping with everyday activities. Therefore there is a call for new models for early intervention and rehabilitation in order to give service to a larger amount of home living people. Reablement is a new and promising rehabilitation model which many Norwegian municipalities are implementing in order to meet current and future needs for municipal home-based services. However, very little research has been performed regarding the effectiveness of this intervention. This study aims at assessing the effectiveness of reablement in terms of daily functioning, health-related quality of life, coping, mental health and economic municipal costs. The study will be conducted in 44 municipalities in Norway. It is a quasi-experimental intervention trial, recruiting home-dwelling adults with an initial functional decline in daily activities. The intervention is intensive, multidisciplinary, home-based rehabilitation given by home-trainers, under supervision from an occupational therapist, nurse or a physiotherapist. The control intervention is standard home-based treatment and care. A total of approximately 750 participants will be recruited, including approximately 100 participants the control group. The participants will be assessed at baseline, and at 10 weeks ,6-, and 12 months follow-up. Primary outcomes will be participation, activity, and municipal expenditures. Costs are generated by the working hours of the different professions. Hence, there will be a weekly registration of the working hours different health care professions spend in the private homes of the participants. Data analyses will be performed according to intention to treat. Univariate analysis of covariance will be used to investigate differences between the groups from baseline to the end of intervention. The working hour data is panel data and will be analyzed accordingly; a random or a mixed effect regression model will be employed. Also, descriptive statistics and simpler tests will be carried out.

Registry
clinicaltrials.gov
Start Date
April 2014
End Date
December 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Frode F. Jacobsen
Responsible Party
Sponsor Investigator
Principal Investigator

Frode F. Jacobsen

Professor

Bergen University College

Eligibility Criteria

Inclusion Criteria

  • Home-dwelling person
  • Applicant of home-based services
  • Above 18 years old
  • Functional decline in at least one activity
  • Able to understand written and oral Norwegian

Exclusion Criteria

  • Cognitive disability
  • Terminal ill
  • Being assessed as needing nursing home placement
  • Being assessed as needing institution-based rehabilitation

Outcomes

Primary Outcomes

Change in score in Canadian Occupational Performance Measure

Time Frame: Baseline, 10 weeks, 6 months and 12 months

Activity and participation will be measured using Canadian Occupational Performance Measure (COPM) The COPM is a measure of a client's self-perception of occupational performance in the areas of self-care, productivity and leisure. Outcome measures for the COPM are: the client's most important problems in occupational performance and a total score of performance and a total score of satisfaction for these problems.

Secondary Outcomes

  • Expenditure(Weekly from baseline to 6 months)
  • Short Physical Performance Battery(Baseline, 10 weeks, 6 months and 12 months)

Study Sites (1)

Loading locations...

Similar Trials