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Clinical Trials/NCT00969020
NCT00969020
Completed
Not Applicable

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.

Regionshospitalet Silkeborg1 site in 1 country72 target enrollmentSeptember 2009

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Quality of Life
Sponsor
Regionshospitalet Silkeborg
Enrollment
72
Locations
1
Primary Endpoint
EQ5D
Status
Completed
Last Updated
13 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 2009
End Date
August 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Martin Vesterby

MD

Regionshospitalet Silkeborg

Eligibility Criteria

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.

Outcomes

Primary Outcomes

EQ5D

Time Frame: 12 months

LOS

Time Frame: up to 5 days

Length of Stay

Secondary Outcomes

  • TUG(day 90)
  • SCL-90-r(day 0)
  • anxiety(Day 90)

Study Sites (1)

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