NCT02298374

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.

Trial Health

15
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Timeline
Completed

Started Nov 2014

Typical duration for not_applicable

Status
withdrawn

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

First Submitted

Initial submission to the registry

October 3, 2014

Completed
29 days until next milestone

Study Start

First participant enrolled

November 1, 2014

Completed
23 days until next milestone

First Posted

Study publicly available on registry

November 24, 2014

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2017

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2017

Completed
Last Updated

April 21, 2017

Status Verified

April 1, 2017

Enrollment Period

2.2 years

First QC Date

October 3, 2014

Last Update Submit

April 20, 2017

Conditions

Mobility LimitationAsthenia

Keywords

RehabilitationEvaluation studiesHome care services

Outcome Measures

Primary Outcomes (1)

  • Change in Activity level (measured by body-worn sensors)

    measured by body-worn sensors over 4 days

    1 years

Secondary Outcomes (5)

  • Change in Short Physical performance battery score

    1 year

  • Change in received hours with homecare services

    1 year

  • Qualys (EQ- 5D)

    1 year

  • Change in IPLOS score

    one year

  • Change in cognitive function (Subscore of the Iplos score)

    one year

Study Arms (2)

Homecare reablement

EXPERIMENTAL

Receives comprehensive assessment and individualized follow-up according to a plan with short and longterm goals.

Other: Homecare reablement

Usual care

ACTIVE COMPARATOR

Receives normal care

Other: usual care

Interventions

Homecare reablementOTHER
Homecare reablement
usual careOTHER
Usual care

Eligibility Criteria

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

You may qualify if:

  • receive homecare services
  • live within the catchment area

You may not qualify if:

  • In-patient length of stay (IPLOS) score \> 2.0
  • severe dementia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Mobility LimitationAsthenia

Condition Hierarchy (Ancestors)

Signs and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Jorunn L Helbostad, phd prof

    Norwegian University of Science and Technology

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 3, 2014

First Posted

November 24, 2014

Study Start

November 1, 2014

Primary Completion

January 1, 2017

Study Completion

June 1, 2017

Last Updated

April 21, 2017

Record last verified: 2017-04