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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: SLCTR
Last refreshed on: 27 April 2013
Main ID:  SLCTR/2008/019
Date of registration: 17/10/2008
Primary sponsor: Dr. L.S Wijeratne
Public title: Mind on arthritis study
Scientific title: Effect of a mind development program on the clinical profile and primary mental health status of patients with rheumatoid arthritis (RA)
Date of first enrolment: 15/6/2008
Target sample size: 175
Recruitment status: Completed
URL:  http://www.slctr.lk/trial_details.asp?reg_id={A57C24E1-D91D-4156-8930-4D4FF76D0649}
Study type:  Interventional
Study design:  A quasi experimental design will be used. Two groups will be selected. One group will receive a mind development exercise in addition to the standard treatment. The other group (comparison group) will receive standard treatment. Pre-intervention assessment of primary mental health status, pain and disability will be done. Assessment of socio-demographic status will be done in both groups to assess the comparability. Post intervention assessments will be done periodically  
Countries of recruitment
Sri Lanka
Contacts
Name: Dr.M.W Gunathunga 
Address:  121/24, Pio Mawatha, Kandana
Telephone: 0714272871
Email: wasantg@hotmail.com
Affiliation:  Senior Lecturer in Communiy Medicine
Name: Dr.M.W Gunathunga 
Address:  121/24, Pio Mawatha, Kandana
Telephone: 0714272871
Email: wasantg@hotmail.com
Affiliation:  Senior Lecturer in Communiy Medicine
Key inclusion & exclusion criteria
Inclusion criteria: Patients above twelve years attending a rheumatology clinic in NHSL
Exclusion criteria: Those patients who have major psychiatric illnesses in the exacerbation phase

Age minimum:
Age maximum:
Gender:
Health Condition(s) or Problem(s) studied
Rheumatoid arthritis
Intervention(s)
A facilitator will conduct the meditation sessions periodically and the patients will be trained to practice it at home in addition to the sessions during clinics
Primary Outcome(s)
1.Reductions in pain in visual analogue scale
2.Reduction in the number of joints affected
3.Improvements in the primary mental health status
Secondary Outcome(s)
1.Duration of symptom free state
2.Duration of sustained improvement of symptoms
Secondary ID(s)
None
Source(s) of Monetary Support
Ministry of Health
Secondary Sponsor(s)
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