ClinicalTrials.gov
ClinicalTrials.gov Menu

Outpatient Treatment of Patients With Morbid Obesity - a Two-year Follow up

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT01249209
Recruitment Status : Completed
First Posted : November 29, 2010
Last Update Posted : November 29, 2010
Sponsor:
Information provided by:
Sykehuset Innlandet HF

Brief Summary:

This study is a pilot project to investigate any effect on these markers in conjunction with lifestyle changes / conservative treatment. Useful and significant information in this pilot project is intended to be used as background for further research on this issue in connection with a doctorate.

What is the effect of two years of outpatient treatment for lifestyle change for weight markers, waist, BMI, HbA1c, HDL and LDL cholesterol, triglycerides and uric acid in adults with morbid obesity?


Condition or disease Intervention/treatment Phase
Morbid Obesity Device: lifestyle advice Not Applicable

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 69 participants
Intervention Model: Single Group Assignment
Primary Purpose: Treatment
Official Title: Qualitative Retrospective Study Where the Intervention Consisted of Group Therapy and Individual Interviews Over a Two-year Period
Study Start Date : May 2010
Actual Primary Completion Date : September 2010
Actual Study Completion Date : October 2010

Arm Intervention/treatment
lifestyle advice Device: lifestyle advice




Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 60 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Adults from 18 - 60 years, both sex

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01249209


Locations
Norway
Sykehuset Innlandet Kongsvinger
Kongsvinger, Norway, 2214
Sponsors and Collaborators
Sykehuset Innlandet HF

Responsible Party: Sykehuset Innlandet HF
ClinicalTrials.gov Identifier: NCT01249209     History of Changes
Other Study ID Numbers: SI HF Kongsvinger
skyrud,randi ( Other Identifier: SykehusetInnlandet )
First Posted: November 29, 2010    Key Record Dates
Last Update Posted: November 29, 2010
Last Verified: June 2010

Keywords provided by Sykehuset Innlandet HF:
obesity
adults
lifestyle intervention
effect after two years treatment for lifestyle change - morbid obesity adults

Additional relevant MeSH terms:
Obesity
Obesity, Morbid
Overnutrition
Nutrition Disorders
Overweight
Body Weight
Signs and Symptoms