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Effect of Healthy Lunch and Snack Meal on Reaction Time and Well-being of Physicians and Nursing Staff (Go-No-Go)

Long-term Effect of Healthy Lunch and Snack Meal on Reaction Time and Well-being: A Randomised Controlled Intervention in Physicians and Nursing Staff.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01739569
Enrollment
60
Registered
2012-12-03
Start date
2012-08-31
Completion date
2012-12-31
Last updated
2022-12-21

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

Conditions

Nutrition Intervention

Keywords

Diet treatment, Mental Health, Reaction time, State of moods, Working hours, Medical Hospital Staff

Brief summary

The aim of this study is to investigate the impact of increased availability of healthy food and drink during working hours on reaction time and well-being in physicians and nursing staff. Hospital medical staff often works long and hectic hours, without adequate meal or rest breaks in order to provide 24-hour care. This is a concern, as not only the staff's well-being is important to the individual welfare, but it is also vital to the quality and safety of the care their patients receive. The investigators believe that by focusing on physicians and nursing staffs nutrition the investigators will see a positive effect on staff performance and well-being - and thus ultimately possibly on patient safety. Hypothesis: The provision of healthy lunch and snack meal during working hours for a period of 4 weeks will improve reaction time and well-being compared to habitual diet in physicians, nurses and nursing assistants.

Detailed description

The study is designed as a randomised controlled 2 x 4 weeks cross-over trial, initiated with a 1-week run-in period. The study sample will consist of 60 volunteer physicians, nurses and nursing assistants from Herlev University Hospital in Copenhagen, Denmark. A healthy lunch and snack meal meeting the current danish diet recommendations will be delivered daily during all working days in the intervention period. During the control period, the participants are requested to maintain their habitual dietary intake at work. Reaction time will be assessed by reaction time test Go/No-Go, a subtest of Test-battery for Attention Performance. Changes in mood will be measured by the Profile of Mood State questionnaire. In addition, dietary intake, level of physical activity and palatability of the intervention diet will be registered.

Interventions

Dietary treatment with healthy lunch and snack meal during working hours

Sponsors

Copenhagen University Hospital at Herlev
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Employed in Herlev University Hospital as physician, nurse or nursing assistant (males and females) * Age 20-70 years * BMI 18,5-30 kg/m2 * Work at least 30 h/wk * Have daily contact with patients and/or have responsibilities that may affect patient safety * Primarily work in day- or evening shifts during the study period * Not having any intentions of loosing weight or changing lifestyle habits during the study period * Not suffer from any diseases that might affect dietary intake (e.g. food allergies, food intolerance) * Not dine in the staff canteen, the Diastole, more than once a week * Be able to write and understand the Danish language

Exclusion criteria

* For those working \>35 h/wk having holiday/ time off duty for more than 9 consecutive days during the study period. * For those working \<35 h/wk having holiday/time off duty for more than 5 consecutive days during the study period * Not to be able to attend the planned tests in the study * Pregnancy * Intensive physical exercise (e.g. strength training) \> 5 hours/wk * Suffer from food allergies or - intolerance

Design outcomes

Primary

MeasureTime frameDescription
Reaction-timeweek 0, week 5 and week 9Differences in reaction-time, as measured by the reaction time test Go/No-Go, a subtest of Test-battery for Attentional Performance from baseline (week 0) to week 4 in the intervention period and week 4 in the control period.

Secondary

MeasureTime frameDescription
Dietary intakeWeek 0, week 5, week 9Differences in dietary intake with respect to macronutrient composition, meal pattern and choice of food items measured by self-reported records during 4 working days using a standardized dietary record form
Physical activityWeek 0, week 5, week 9Differences in 24-hours physical activity measured by self-reported records during four working days using a standardized physical activity record form.
Palatability of the diet eaten during working hoursWeek 0, week 5 and week 9Differences in palatability of the intervention diet compared to the control diet measured by scores using a specific and standardized Visual Analouge Scale (VAS-scores).
Well-beingWeek 0, week 5 and week 9Differences in selfreported well-being, as measured by the POMS Questionaire (McNair et.al. Manual of the Profile of Mood States. San Diego:Educational and Industrial Testing Service;1981) form baseline (week 0) to week 4 in the intervention period and week 4 in the control period.

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026