Skip to content

Interventions for Lifestyle Changes to Promote Weight Reduction, a Randomized Controlled Trial in Primary Health Care

Interventions for Lifestyle Changes to Promote Weight Reduction, a Randomized Controlled Trial in Primary Health Care

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01606917
Acronym
LÄTTA
Enrollment
133
Registered
2012-05-28
Start date
2004-10-31
Completion date
2011-10-31
Last updated
2012-05-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overweight/Obesity

Brief summary

The purpose of this study is to examine the effects of a weight reduction program in adults, seen in a primary care setting, with overweight/obesity perceived as a health problem or with diseases related to overweight/obesity and ambitions to achieve weight reduction as part of treatment.

Detailed description

Patients seeking advice for overweight/obesity or illness related to overweight/obesity at eight primary health care centers in Sweden were randomized either to intervention or control care groups with both dietary advice and individualized advice on increased regular physical activity. Main outcome measures were reduction in body weight of 5 percent or more from study start.

Interventions

Both dietary advice and individualized advice on increased regular physical activity

Sponsors

Örebro County Council
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Proportion of patients who achieved target weight at two years2 years

Secondary

MeasureTime frame
Clinical or laboratory manifestations of their baseline illness (type 2 diabetes, hypertension, CHD, dyslipidemia) or death of any cause.5 years

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 23, 2026