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Main
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Note: This record shows only 22 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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01606917 |
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Date of registration:
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24/05/2012 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Interventions for Lifestyle Changes to Promote Weight Reduction, a Randomized Controlled Trial in Primary Health Care
LÄTTA |
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Scientific title:
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Interventions for Lifestyle Changes to Promote Weight Reduction, a Randomized Controlled Trial in Primary Health Care |
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Date of first enrolment:
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October 2004 |
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Target sample size:
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133 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01606917 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Sweden
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Contacts
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Name:
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Stefan P.O Jansson, MD PhD student |
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Address:
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Telephone:
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Email:
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Affiliation:
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Family Medicine Research Centre, Örebro County Council, School of Health and Medical Sciences, Örebro University |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Adult patients between 18 and 70 years of age who consulted or were in care for
overweight/obesity with or without type 2 diabetes
- Hypertension, CVD
- Coronary heart disease (CHD)
- Dyslipidemia
- Gallstone or musculoskeletal disorders
Exclusion Criteria:
- Patients were not eligible if they were already taking part in another weight control
program
- Understood the Swedish language poorly
- Were mentally ill or had an alcohol or drug addiction.
- Nor were they eligible if they had a physical disability preventing intensified
physical activity or were pregnant at study start.
Age minimum:
18 Years
Age maximum:
70 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Overweight/Obesity
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Intervention(s)
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Other: Intensive lifestyle counseling
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Primary Outcome(s)
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Proportion of patients who achieved target weight at two years
[Time Frame: 2 years]
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Secondary Outcome(s)
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Clinical or laboratory manifestations of their baseline illness (type 2 diabetes, hypertension, CHD, dyslipidemia) or death of any cause.
[Time Frame: 5 years]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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