In this study we will assess the (cost)effectiveness of a transmural integrated care programme supporting return to daily activities (including work)after knee arthroplasty compared to usual care. We hypothesize our transmural integrated care…
ID
Source
Brief title
Condition
- Joint disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The primary outcome measure will be quality of life.
Secondary outcome
Secondary outcome will be (work) participation.
Background summary
In 2030, there will be an estimated 57,900 knee arthroplasties in the
Netherlands, with about half of these patients expected to be in working age.
Three out of 10 Dutch knee arthroplasty patients do not return to work at all
and only 50% of the patients return to work within 3 months, which has an major
impact on patient*s quality of life.
Study objective
In this study we will assess the (cost)effectiveness of a transmural integrated
care programme supporting return to daily activities (including work)
after knee arthroplasty compared to usual care. We hypothesize our transmural
integrated care intervention to increase (work) participation and quality of
life, which will reduce healthcare and work absenteeism costs.
Study design
A randomized controlled trial with economic evaluation.
Intervention
The intervention under study will consist of a a transmural integrated care
program, including: 1) active referral to a case-manager (e.g. an
occupational/physical therapist), 2) a rehabilitation program based on patient
specific participation goal attainment , and 3) a patient tailored m/eHealth
intervention (using the existing portal ikherstel.nl linked with activity
trackers to provide feedback on achievement of activity goals). People receving
this intervention will be compared with those receiving care as usual
consisting of knee arthroplasty surgery and subsequent care, in accordance to
the guidelines of the Dutch Orthopaedic Association (NOV).
Study burden and risks
We expect the risk of participation in this study to be negligible. The only
burden that will be put on participation is that they will have spend their
time (approximately 10 hours per patient) to participating in our study.
van der Boechorststraat 7
Amsterdam 1081BT
NL
van der Boechorststraat 7
Amsterdam 1081BT
NL
Listed location countries
Age
Inclusion criteria
Patients from the working age (18-67 jaar) with a paid job >8hrs a week who
will undergo knee replacement surgery will be included.
Exclusion criteria
We will exclude participants who are not able to provide informed concent or
who have insufficient understanding of the Dutch language
Design
Recruitment
Medical products/devices used
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
| Register | ID |
|---|---|
| CCMO | NL67692.029.18 |