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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01336725
Other study ID # S-08662c 2008/17575 (REK)
Secondary ID
Status Completed
Phase N/A
First received April 14, 2011
Last updated April 15, 2011
Start date January 2009
Est. completion date December 2010

Study information

Verified date April 2011
Source Oslo University Hospital
Contact n/a
Is FDA regulated No
Health authority Norway:National Committee for Medical and Health Research Ethics
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine whether the participants have improved their scores on health related quality of life (HRQL) 1 year after completing a learning and mastery course and whether sociodemographic variables are associated with HRQL.


Description:

Persons with chronic illnesses have to adjust to changes in their life-style. In the last 10 years Learning and Mastery Centres have been established in Norwegian hospitals to offer patient education for the chronically ill. It is not known whether these courses impact any changes in HRQL 1 year after course completion.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date December 2010
Est. primary completion date September 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- diagnosis of morbid obesity

- attending learning and mastery course for the obese

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Behavioral:
Teaching life style changes
Single group: Teaching, group sessions, physical activity
Other:
Active participation
Obesity group attend 10 group sessions,are informed about and discuss needed life style changes such as weight loss and participate in physical activity and cooking.
Teaching
Morbid obesity group attend 40 hours of group sessions

Locations

Country Name City State
Norway Oslo universiy hospital, Aker Oslo

Sponsors (1)

Lead Sponsor Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Health related quality of life 1 year after course completion No
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