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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:  NTR843
Date of registration: 14/12/2006
Primary sponsor: VU University Medical Center, Department of Rehabilitation Medicine
Public title: Efficacy of client-centred occupational therapy in patients with multiple sclerosis: a cluster-randomised trial.
Scientific title: Efficacy of client-centred occupational therapy in patients with multiple sclerosis: a cluster-randomised trial. - MUSCOT
Date of first enrolment: 1/1/2007
Target sample size: 280
Recruitment status: pending
URL:  http://www.trialregister.nl/trialreg/admin/rctview.asp?TC=843
Study type:  intervention
Study design:  Randomised: Yes; Masking: Double; Control: Active; Group: Parallel; Type: -  
Countries of recruitment
The Netherlands
Contacts
Name: I.C.J.M. (Isaline)  Eyssen
Address:  VU University Medical Center, Department of Rehabilitation Medicine, Occupational and Physical Therapy, P.O. Box 7057 1007 MB Amsterdam The Netherlands
Telephone: +31 (0)20 4440012
Email: i.eyssen@vumc.nl
Affiliation: 
Name: M.P.M. (Martijn)  Steultjens
Address:  VU University Medical Center, Department of Rehabilitation, Occupational and Physical Therapy, P.O. Box 7057 1007 MB Amsterdam The Netherlands
Telephone: +31 (0)20 4443063
Email: m.steultjens@vumc.nl
Affiliation: 
Key inclusion & exclusion criteria
Inclusion criteria: 1. Diagnosed Multiple Sclerosis;
2. New referral for occupational therapy;
3. Age between 18 and 75 years.
Exclusion criteria: 1. Major depression.

Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
Multiple sclerosis (MS)

Intervention(s)
Experimental intervention: client-centred occupational therapy accoridng to the Occupational Performance Process Model (OPPM)

Control intervention: usual-care occupational therapy
Primary Outcome(s)
1. Disability Impact Profile (DIP) questionniare;
2. Impact on Participation and Autonomy (IPA) questionnaire.
At baseline) and after 4 and 8
months follow-up.
Secondary Outcome(s)
1. Evaluation of Client-Centred Process (ECGP) questionnaire;
2. Quality of Care through the patient's eyes (QUOTE-EEE) questionnaire;
3. Canadian Occupational Performance Measure (COPM);
4. 9HPT Dexterity measure;
5. Fatigue (MFIS) questionnaire.
6. Pain (PES) questionnaire;
7. Cognitive functioning (PDQ) questionnaire;
8. Generic Health-related Quality of Life (SF-36) questionnaire.
At baseline) and after 4 and 8
months follow-up.
Secondary ID(s)
ISRCTN85468190
N/A
Source(s) of Monetary Support
Stichting MS Research
Secondary Sponsor(s)
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