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The Lifestyle moDIfCation Study

A Before-and-after Study to Evaluate Effects of Low-cost Interventions for Promoting Healthy Lifestyle Modifications

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01574040
Acronym
LUDIC
Enrollment
11000
Registered
2012-04-10
Start date
2012-02-29
Completion date
Unknown
Last updated
2012-04-10

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

Conditions

Healthy

Keywords

Lifestyle, Lifestyle modification, Behavior, Primary prevention, Healthy staff and visitors of an Academic Hospital

Brief summary

Rationale: Lifestyle modifications, such as increasing physical exercise and reducing dietary salt and saturated fat intake contribute to prevention of cardiovascular morbidity and mortality. Relevant improvements can already be achieved by small adaptations in everyday life. It is unclear whether simple low-cost interventions in the working environment can promote such healthy lifestyle adaptations. Objective: To study the effect of low-cost interventions for promoting healthy lifestyle modifications. Study design: Before-and-after intervention study. The study period will be subdivided in four parts of 2 weeks each: a run-in period, a before-measurement period, an intervention-period, and an after measurement period. Study population: Staff and visitors of the University Medical Center Utrecht. Study interventions: * Promotion of stair climbing. * Promotion of a low-salt soup alternative for the 'soup of the day'. * Promotion of a low-fat alternative for the butter croissants. * Exchange of the basket positions of butter and margarine between convenient and harder to reach locations. Outcome measures: * Number of passages through each part of the stair cases. * Number of low-salt cream soup and normal clear soup cups sold in the hospital restaurant and ratio between them. * Number of low-fat and normal croissants sold in the hospital restaurant and the ratio between them. * Number of low-fat margarine servings and butter servings sold in the hospital restaurant and the ratio between them.

Detailed description

Detailed description of the study periods: * Run-in period: during the first 2 weeks of the study (day 1 until day 14) the baseline situation should be established and remain stable. This period is meant for study personnel to get acquainted with the study procedures. * Before-measurement: during weeks 3 and 4 (day 15 until day 28) the measurements will start to record all endpoints and additional parameters during the baseline situation. * Intervention-period: during weeks 5 and 6 (day 29 until day 42) the measurements will continue while the interventions are carried out. * After measurement: during weeks 7 and 8 (day 43 until day 56) the measurements will continue while the interventions have ended and the baseline situation is restored.

Interventions

BEHAVIORALPromotion of stair climbing

Application of labels on all UMC elevator doors stating: If you take the stairs, you will burn 11 times more calories.

BEHAVIORALPromotion of a low-salt soup alternative for the 'soup of the day'

Promotion of a low-salt soup alternative for the 'soup of the day' in the UMC staff restaurant, using a sign stating: The cream soup contains 30% less salt and contributes to a healthy blood pressure.

BEHAVIORALPromotion of a low-fat alternative for the butter croissants

Promotion of a low-fat alternative for the butter croissants in the UMC staff restaurant, using a sign stating: This croissant contains 30% fewer saturated (unhealthy) fatty acids.

BEHAVIORALExchange of the basket positions of butter and margarine in the UMC staff restaurant between convenient and harder to reach locations

Exchange of the basket positions of butter and margarine in the UMC staff restaurant. In the usual (baseline) situation butter is positioned in the fridge and, therefore, less visible and harder to reach. Margarine is positioned on several convenient locations throughout the restaurant. During the two weeks intervention period these positions will be interchanged.

Sponsors

UMC Utrecht
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

Dynamic population of staff and visitors of the University Medical Center Utrecht, The Netherlands

Design outcomes

Primary

MeasureTime frameDescription
Number of passages through each part of the stair cases2 weeks (including weekend days)Measured by wireless infrared interruption counters
Number of low-salt cream soup and normal clear soup cups sold in the hospital restaurant and ratio between them2 weeks (excluding weekend days)Assessed by the pay desk computer system administration
Number of low-fat and normal croissants sold in the hospital restaurant and the ratio between them2 weeks (excluding weekend days)Number of croissants sold will be registered on daily work sheets by the restaurant personnel
Number of low-fat margarine servings and butter servings sold in the hospital restaurant and the ratio between them2 weeks (excluding weekend days)Assessed by the pay desk computer system administration

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026