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A Telemedicine Solution for Remote Support of Rehabilitation, for Patients Undergoing, Total Hip Arthroplasty Surgery

The Effect of Remote Rehabilitation Support Via a Telemedicine Solution for Patients Undergoing an Optimized Fast-track Orthopedic Surgery Procedure With the Implementation of a Total Hip Arthroplasty.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00969020
Acronym
RRS
Enrollment
72
Registered
2009-08-31
Start date
2009-09-30
Completion date
2012-08-31
Last updated
2012-10-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Quality of Life

Keywords

Length of stay, Timed up and go

Brief summary

The RRS project is a Randomized Clinical Trial documenting the effect of Remote Rehabilitation and Support via a telemedicine solution for patients undergoing an optimized fast-track orthopedic surgery procedure with the implementation of a total hip arthroplasty. With the telemedicine solution the investigators will support and try to motivate the patient to be discharged after only one day of hospitalization.

Detailed description

This PhD study evaluates the effect of an information technology solution containing RRS. The way it supports, informs and educates the patient and support person, provides an opportunity for communication between the patient and the surgeons, physiotherapists and nurses at the hospital. The parameters evaluated will be: Length of stay, health-related quality-of-life (HRQOL), functional outcome, pain, anxiety, complications and an evaluation of the socio-economic effect. The aim of the study generates the following hypotheses and focus for publication * Length of stay is lower for the intervention group compared to the control group. * The average quality of life measured with EQ-5D will either be the same or higher when comparing the intervention group with the control group. * Compared to the control group the functional outcome of the intervention group measured with Oxford Hip Score (OHS) and Timed Up and Go (TUG) will be the same or better. * Complications measured as luxations, infections, and reoperations are the same or lower in the intervention group compared to the control group. * There will be a correlation between patients with the highest level of psychological problems and symptoms of psychopathology measured with Symptom Checklist-90-R, and the postoperative outcome measured with EQ5D, anxiety and TUG. * There will be a correlation between support persons with the highest level of psychological problems and symptoms of psychopathology measured with Symptom Checklist-90-R, and the postoperative outcome measured with EQ5D, anxiety and TUG for the patient they are related to. * The socio-economic costs will be lower for the intervention group compared to the control group based on self reported data and data collected from official databases. This study will be conducted as a piggy back to the RCT.

Interventions

PROCEDUREremote rehabilitation support

An information technology solution containing RRS. The way it supports,, informs and educates the patient and support person, provides an opportunity for communication between the patient and the surgeons, physiotherapists and nurses at the hospital.

Sponsors

Caretech Innovation
CollaboratorUNKNOWN
Lundbeck Foundation
CollaboratorOTHER
Regionshospitalet Silkeborg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients qualified to go trough at joint-care procedure after the guidelines from Regionshospitalet Silkeborg.

Exclusion criteria

* Previous hip surgery with the implantation of a total hip arthroplasty. * Patients living more than approximately 60 kilometers from the Regionshospitalet Silkeborg. * Patients with no 3G tele-net at their home address. * Patients with the need of Danish interpretation.

Design outcomes

Primary

MeasureTime frameDescription
EQ5D12 months
LOSup to 5 daysLength of Stay

Secondary

MeasureTime frameDescription
SCL-90-rday 0psychological problems and symptoms of psychopathology
TUGday 90Time up and go
anxietyDay 90VAS - anxiety

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026