World Health Organization site
Skip Navigation Links

Main
Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: Netherlands Trial Register
Last refreshed on: 28 April 2013
Main ID:  NTR1695
Date of registration: 04/03/2009
Primary sponsor: Roessingh Research and Development b.v.
Public title: Evaluation of the Online Exercise Coach.
Scientific title: Evaluation of the Online Exercise Coach. - Online Exercise Coach
Date of first enrolment: 15/12/2008
Target sample size: 56
Recruitment status: recruiting
URL:  http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=1695
Study type:  intervention
Study design:  Randomised: Yes; Masking: [default]; Control: Active; Group: Parallel; Type: 2 or more arms, randomized  
Countries of recruitment
The Netherlands
Contacts
Name: K.  Cranen
Address:  , Roessingh Research and Development Roessinghsbleekweg 33b 7522 AH Enschede The Netherlands
Telephone: +31 (0)53 487 5758
Email: k.cranen@rrd.nl
Affiliation: 
Name: K.  Cranen
Address:  , Roessingh Research and Development Roessinghsbleekweg 33b 7522 AH Enschede The Netherlands
Telephone: +31 (0)53 487 5758
Email: k.cranen@rrd.nl
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1. Chronic low back pain;

2. RSI;

3. Whiplash;

4. Age of 18 years or older.

Exclusion criteria: Insufficient control of the Dutch language.

Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
Chronic pain

Intervention(s)
Subjects in the experimental group will receive six weeks of OEC follow-up treatment. Patients have access to their online tailored exercise programs by logging onto the website www.r-motion.nl. Patients? former policlinic therapist will select a broad range of exercises from which the patient can choose from to create his own exercise programme. The exercises consist of mobilizing, muscle strengthening and conditional exercises. In addition patients have the opportunity to view the exercises on their computer by playing the video-files on the website. Also they are offered an email function on the website where they can contact their therapist in case they have questions about their exercises.
The control group comprises of a six week exercise follow-up program by means of once-only instruction by word of mouth at the end of the policlinic treatment at ?Het Roessingh?. If patients experience problems during their six weeks of follow-up treatment they are instructed to call their therapist.
Patients in both the intervention and control group are asked to exercise for 30 minutes 3 times a week.
Primary Outcome(s)
The primary objective is to investigate if the use of the Online Exercise Coach enhances compliance with the follow-up exercise program. Therefore the primary objective is:


1. Are patients who used the OEC during their follow-up exercise treatment more compliant than patients who did not use the OEC?
Secondary Outcome(s)
Preferences:

1. What are the preferences of chronic pain patients regarding exercise follow-up treatment?

A. Do chronic pain patients prefer the OEC or the traditional advice as exercise follow-up treatment?

B. Which attributes of OEC and traditional advice exercise follow-up treatment are considered as most important by chronic pain patients?

2. Do exercise follow-up treatment preferences change after patients completed their follow-up treatment?


Satisfaction:

3. How satisfied are patients on the factors of the intention-based models (such as the TPB and TAM model: attitude, self-efficacy and/or social support, perceived ease of use and perceived usefulness)?

4. Is the technical performance of the OEC sufficient for clinical use from the end user perspective?


Clinical Effectiveness:

5. Do patients? interference of pain, actual pain levels, pain related fear of movement and general health change after six weeks of exercise follow-up treatment?

6. Do patients who used the OEC during their follow-up score better on interference of pain, actual pain levels, pain related fear of movement and general health than patients who did not use the OEC?
Secondary ID(s)
Roessingh Research & Development
Source(s) of Monetary Support
Roessingh Research & Development
Secondary Sponsor(s)
Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.
Copyright - World Health Organization - Version 3.1 - Version history