Evaluation of Homecare Reablement, the Trondheim Model
Primary Purpose
Mobility Limitation, Asthenia
Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Homecare reablement
usual care
Sponsored by
About this trial
This is an interventional prevention trial for Mobility Limitation focused on measuring Rehabilitation, Evaluation studies, Home care services
Eligibility Criteria
Inclusion Criteria:
- receive homecare services
- live within the catchment area
Exclusion Criteria:
- In-patient length of stay (IPLOS) score > 2.0
- severe dementia
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Homecare reablement
Usual care
Arm Description
Receives comprehensive assessment and individualized follow-up according to a plan with short and longterm goals.
Receives normal care
Outcomes
Primary Outcome Measures
Change in Activity level (measured by body-worn sensors)
measured by body-worn sensors over 4 days
Secondary Outcome Measures
Change in Short Physical performance battery score
Performance based test of lower extremity function
Change in received hours with homecare services
Including nursing, assistance in activities of daily living and domestic work
Qualys (EQ- 5D)
EQ- 5D
Change in IPLOS score
A composite score on level of dependency in 17 different areas related to activities of daily living, including cognitive function
Change in cognitive function (Subscore of the Iplos score)
Subscore of the Iplos score
Full Information
NCT ID
NCT02298374
First Posted
October 3, 2014
Last Updated
April 20, 2017
Sponsor
Norwegian University of Science and Technology
Collaborators
Trondheim Kommune, St. Olavs Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02298374
Brief Title
Evaluation of Homecare Reablement, the Trondheim Model
Official Title
Evaluation of Homecare Reablement, the Trondheim Model
Study Type
Interventional
2. Study Status
Record Verification Date
April 2017
Overall Recruitment Status
Withdrawn
Why Stopped
no funding
Study Start Date
November 2014 (undefined)
Primary Completion Date
January 2017 (Anticipated)
Study Completion Date
June 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Norwegian University of Science and Technology
Collaborators
Trondheim Kommune, St. Olavs Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim is to evaluate a model of home-based rehabilitation. The intervention targets elder persons who receive homecare services, but still are relatively independent in most activities of daily living. The model focuses on early identification of decline in function and intervention in the home environment through close cooperation between the participant, homecare services and therapists.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mobility Limitation, Asthenia
Keywords
Rehabilitation, Evaluation studies, Home care services
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Homecare reablement
Arm Type
Experimental
Arm Description
Receives comprehensive assessment and individualized follow-up according to a plan with short and longterm goals.
Arm Title
Usual care
Arm Type
Active Comparator
Arm Description
Receives normal care
Intervention Type
Other
Intervention Name(s)
Homecare reablement
Intervention Type
Other
Intervention Name(s)
usual care
Primary Outcome Measure Information:
Title
Change in Activity level (measured by body-worn sensors)
Description
measured by body-worn sensors over 4 days
Time Frame
1 years
Secondary Outcome Measure Information:
Title
Change in Short Physical performance battery score
Description
Performance based test of lower extremity function
Time Frame
1 year
Title
Change in received hours with homecare services
Description
Including nursing, assistance in activities of daily living and domestic work
Time Frame
1 year
Title
Qualys (EQ- 5D)
Description
EQ- 5D
Time Frame
1 year
Title
Change in IPLOS score
Description
A composite score on level of dependency in 17 different areas related to activities of daily living, including cognitive function
Time Frame
one year
Title
Change in cognitive function (Subscore of the Iplos score)
Description
Subscore of the Iplos score
Time Frame
one year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
receive homecare services
live within the catchment area
Exclusion Criteria:
In-patient length of stay (IPLOS) score > 2.0
severe dementia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jorunn L Helbostad, phd prof
Organizational Affiliation
Norwegian University of Science and Technology
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Evaluation of Homecare Reablement, the Trondheim Model
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