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Treatment of Overweight in General Practice

Treatment of Overweight in General Practice

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03000062
Enrollment
23
Registered
2016-12-21
Start date
2017-01-31
Completion date
2019-12-31
Last updated
2021-06-22

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

Conditions

Nutritional and Metabolic Diseases, Overweight and Obesity

Keywords

overweight, general practice

Brief summary

In this study the investigators want to explore the feasibility and effect of a simple intervention provided by primary care physicians on treatment for overweight in general practice. Regular patients visiting their ordinary family physician will be asked for participation if they comply with the inclusion criteria. If so, they will follow a detailed food list for 12 months with regular visits to the doctor. At each visit, the participating patients will be asked about their progress on weight loss and all measurements will be made. Simultaneously a control group of primary care physicians will also recruit patients that fulfill the inclusion criteria. These patients will also provide data that will serve as Control to the intervention group.

Detailed description

The number of patients with overweight is increasing and a daily issue in general practice. Many patients wish to discuss their weight problem with their family physician but many of these feel helpless to guide their patients in how to reduce weight. Providing useful and correct information should not be so difficult but many doctors choose to refer their patients to dietary courses or follow-up in specialist health care.In this study the investigators wish to implement a simple tool for treatment of overweight in primary care by providing the patients a detailed list for all meals that will ensure a weight loss. The patients will be given a close follow-up by their doctor, and the motivating conversation and list of meals will be the only treatment given. The study is a cluster randomised controlled trial where all general practices in the area of Moss city in Norway will be asked to participate. Half of the physicians will constitute the intervention group while the other half will serve as control group. Each participating doctor in both groups will recruit patients according to the eligibility criteria. The doctors in the intervention group will be provided with a course to learn the intervention and have a manual to follow for each patient. All participating patients of both groups will be asked to meet regularly for data collection. According to the power calculation, a number of 12 physicians in each group will be sufficient if they recruit 10 patients each. The intervention will be conducted for 12 months and thereafter data will be continued to be collected at 6 and 12 months after.

Interventions

BEHAVIORALIntervention group

Please see the preceding section

Sponsors

University of Oslo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

ID of participating patients are only available through the participating Family phyisican

Intervention model description

Cluster randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 69 Years
Healthy volunteers
Yes

Inclusion criteria

* BMI \_\> 30 OR \_25 With at least one Medical condition related to overweight (hypertension, dyslipidemia, metabolic syndrome, diabetes mellitus II, hip- or knee pain) * written consent * sufficient knowledge in Norwegian Language to acquire the written and oral information

Exclusion criteria

* any ongoing cancer condition * any current medication impacting on weight

Design outcomes

Primary

MeasureTime frameDescription
Weight reduction12 months10% weight reduction measured as kilo weight at inclusion

Secondary

MeasureTime frameDescription
Blood pressure12 monthsBlood pressure measured as mean of three measurements at rest
HbA1c12 monthsBlood samples
Waist measure12 monthsAny reduction in cm of waist measure
Total Cholesterol12 monthsBlood samples

Other

MeasureTime frameDescription
Qualitative study24 monthsParticipating physicians and patients will be interviewed about their experiences With the intervention

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026