- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01336725
Learning and Coping With Chronic Illness
April 15, 2011 updated by: Oslo University Hospital
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.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed 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.
Study Type
Observational
Enrollment (Anticipated)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Oslo, Norway, 0514
- Oslo universiy hospital, Aker
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Learning and mastery centre
Description
Inclusion Criteria:
- diagnosis of morbid obesity
- attending learning and mastery course for the obese
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Morbid obesity
All attending learning and mastery courses for persons with morbid obesity
|
Single group: Teaching, group sessions, physical activity
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.
Morbid obesity group attend 40 hours of group sessions
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Health related quality of life
Time Frame: 1 year after course completion
|
1 year after course completion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Lerdal A, Gay CL, Bonsaksen T, Fagermoen MS. Predictors of physical and mental health in persons with morbid obesity attending a patient education course - a two-year follow-up study. Health Qual Life Outcomes. 2017 May 15;15(1):103. doi: 10.1186/s12955-017-0675-z.
- Andenaes R, Fagermoen MS, Eide H, Lerdal A. Changes in health-related quality of life in people with morbid obesity attending a learning and mastery course. A longitudinal study with 12-months follow-up. Health Qual Life Outcomes. 2012 Aug 18;10:95. doi: 10.1186/1477-7525-10-95.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2009
Primary Completion (Actual)
September 1, 2010
Study Completion (Actual)
December 1, 2010
Study Registration Dates
First Submitted
April 14, 2011
First Submitted That Met QC Criteria
April 15, 2011
First Posted (Estimate)
April 18, 2011
Study Record Updates
Last Update Posted (Estimate)
April 18, 2011
Last Update Submitted That Met QC Criteria
April 15, 2011
Last Verified
April 1, 2011
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- S-08662c 2008/17575 (REK)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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