Environmental and educational intervention in communal catering to lower salt intake in the Swiss working population

Organizational Data

DRKS-ID:
DRKS00006790
Recruitment Status:
Recruiting complete, study complete
Date of registration in DRKS:
2014-09-23
Last update in DRKS:
2019-09-12
Registration type:
Prospective

Acronym/abbreviation of the study

Gesund+Gut: Na Klar!

URL of the study

No Entry

Brief summary in lay language

Background: High salt intake is a risk factor for cardiovascular disease. The Swiss salt strategy therefore seeks to gradually reduce salt intake to the international recommendation of five grams per day. The investigation looks at the impact of various measures to reduce salt intake among test participants who regularly take their meals at staff restaurants. Aim: Many workers regularly take lunch at a company-provided staff restaurant. This study investigates how salt intake and the associated blood pressure of the working population can be reduced by means of measures in relation to promoting health within the workplace. This is done by gradually optimising the salt content in the food offered by the staff restaurants of voluntarily participating companies over the course of one year. During the same period, the kitchen staff and staff restaurant users are given theoretical information and practical advice on health eating. The purpose of these measures is to motivate the participants in the study and support them in gradually improving their skills, attitudes, and habits in relation to food preparation and consumption. The salt content of the meals offered is investigated in the laboratory. The salt intake, blood pressure, weight, size and health awareness of study participants are also assessed. Finally, the results are compared with those collected from companies that have not changed their staff restaurant offering. Significance: The project is delivering new findings on the factors that encourage or prevent the implementation of health promotion measures in companies and staff restaurants. It will show the extent to which general health can be promoted at low cost. The findings will allow measures intended to reduce salt intake to be assessed in relation to their practical relevance and transferability. This will allow for feasible catering and training plans to be created, and other activities to promote healthy living to be developed at policy, corporate and individual levels.

Brief summary in scientific language

Reducing salt intake at the population level is considered a promising and cost-effective means to reduce cardiovascular disease risk. The Swiss Salt Strategy is pursuing an average salt intake of <8g per person per day at the population level (a 16% reduction) as intermediate goal. For the longer term, the aim is to decrease the intake to 5g/day, as recommended by WHO. Measures should address the overall salt intake distribution in the typical Swiss diet focusing on a stepwise reduction of salt content in major food sources, including offers by the food service industry, and taking into account consumers health literacy and related behaviours. A one year, four-phased community trial is planned in organizations/staff canteens in German-speaking Switzerland, with an intervention and a control group (up to 400 consumers each, 15-65 yrs old from matching canteens; 2x8 clusters,). The objective is to demonstrate the effectiveness of a combined progressive environmental and nutrition educational/motivational intervention in the workplace in reducing the consumers average daily total dietary salt intakes by 16% or more (according to the Swiss salt strategy intermediate goal). For the intervention group the luncheons’ salt contents are reduced step by step, i.e. 4% per phase (total 4x4% = 16% reduction) and concurrently study participants are provided with increasingly specific information (knowledge and skills) on how to put a nutritionally well-balanced diet into action. The consumers in the control group are being served habitual luncheons and they have access to publicly available, general information on healthy eating only. Outcome measures are changes in sodium/salt intake (24 hour and spot urine collection), blood pressure, overall diet composition (3 day food record checklist), anthropometric indices (weight, height, waist and hip circumference) and health literacy (health literacy questionnaire) in the intervention as compared with the control group. Measures are taken at 0/3/6/9/12 months and 0/6/12 months for the intervention and control group, respectively. The community trial will help identifying barriers and promoters for participation of organizations, their staff canteens and their employees. It will demonstrate the practical relevance, and in consequence, the exportability of the shown effectiveness of the intervention elements. The research results should be incorporated in the establishment of easily applicable concepts which facilitate manufacturing/providing and consuming a healthy diet for a healthy life. Note: The intended cluster (organization) randomization proved infeasible. Organizations interested in participation did not accept random allocation to arm 1 (intervention) or arm 2 (control).

Health condition or problem studied

ICD10:
I10.9
Free text:
High salt intake (lifestyle risk factor)
Healthy volunteers:
No Entry

Interventions, Observational Groups

Arm 1:
Up to 8 intervention organizations/staff restaurants are compared with control organiszations (clusters), with up to 50 participants each. Assisted salt reduction program (4x4%, food analysis) of nutritional adequate food supply, implementing Swiss quality standards for health-promoting communal catering. Education program, providing participants with progessively specific information on how to put a health-promoting salt-reduced tasty diet in action. Salt intake (24h/spot urine), blood pressure, anthropometrics, health literacy measured at 0/3/6/9/12 months.
Arm 2:
Control: no change to food supply (food analysis) and no education program (measures at 0/6/12 months)

Endpoints

Primary outcome:
Sodium (Na)/salt intake; Method of measurement: 24 hour a/o spot urine Na excretion; Timepoints: Baseline, 3, 6, 9 and 12 months
Secondary outcome:
Overall qualitative diet composition (Na/K ratio); Blood Pressure; Anthropometrics (weight, height; waist and hip circumferences); Health/Food literacy

Study Design

Purpose:
Prevention
Allocation:
Non-randomized controlled study
Control:
  • Control group receives no treatment
Phase:
N/A
Study type:
Interventional
Mechanism of allocation concealment:
No Entry
Blinding:
No
Assignment:
Parallel
Sequence generation:
No Entry
Who is blinded:
No Entry

Recruitment

Recruitment Status:
Recruiting complete, study complete
Reason if recruiting stopped or withdrawn:
No Entry

Recruitment Locations

Recruitment countries:
  • Switzerland
Number of study centers:
Multicenter study
Recruitment location(s):
  • Other Unternehmen mit Personalrestaurant Kantone BE, AG, SO, BL, BS, LU, ZG und ZH

Recruitment period and number of participants

Planned study start date:
2015-01-01
Actual study start date:
2015-03-23
Planned study completion date:
No Entry
Actual Study Completion Date:
2016-11-04
Target Sample Size:
800
Final Sample Size:
145

Inclusion Criteria

Sex:
All
Minimum Age:
15 Years
Maximum Age:
65 Years
Additional Inclusion Criteria:
15-65 years old employees of organizations with staff restaurant; eating at least 2 times/week in staff restaurant; available for 5 education sessions during 12 months; sufficiently literate in German to read/complete forms/questionnaires and follow education program.

Exclusion Criteria

Medical or non-medical indication and/or medication that interfer with urine collection/analyses; Women being pregnant at time of recruitment; severe food allergy, intolerance or aversion hampering staff restaurant use.

Addresses

Primary Sponsor

Address:
Institut für Sozial- und Präventivmedizin, Universität Bern
Dipl. Oec-troph. UNIV. Sigrid Beer-Borst
Mittelstrasse 43
3012 Bern
Switzerland
Telephone:
+41 79 6206243
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.ispm.ch
Investigator Sponsored/Initiated Trial (IST/IIT):
Yes

Contact for Scientific Queries

Address:
Institut für Sozial- und Präventivmedizin, Universität Bern
Dipl. Oec-troph. UNIV. Sigrid Beer-Borst
Mittelstrasse 43
3012 Bern
Switzerland
Telephone:
+41 79 6206243
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.ispm.ch

Contact for Public Queries

Address:
Institut für Sozial- und Präventivmedizin, Universität Bern
Dipl. Oec-troph. UNIV. Sigrid Beer-Borst
Mittelstrasse 11
3012 Bern
Switzerland
Telephone:
+41 79 6206243
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.ispm.ch

Principal Investigator

Address:
Institut für Sozial- und Präventivmedizin, Universität Bern
Dipl. Oec-troph. UNIV. Sigrid Beer-Borst
Mittelstrasse 43
3012 Bern
Switzerland
Telephone:
+41 79 6206243
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.ispm.ch

Sources of Monetary or Material Support

Public funding institutions financed by tax money/Government funding body (German Research Foundation (DFG), Federal Ministry of Education and Research (BMBF), etc.)

Address:
Schweizerischer Nationalfonds
Wildhainweg 3
3001 Bern
Switzerland
Telephone:
No Entry
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.snf.ch

Private sponsorship (foundations, study societies, etc.)

Address:
Schweizerische Herzstiftung
Schwarztorstrasse 18, Postfach 368
3000 Bern 14
Switzerland
Telephone:
41 31 388 80 82
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.swissheart.ch

Ethics Committee

Address Ethics Committee

Address:
Kantonale Ethikkommission Bern (KEK)
Postfach 56
CH-3010 Bern
Switzerland
Telephone:
No Entry
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.kek-bern.ch/

Vote of leading Ethics Committee

Vote of leading Ethics Committee
Date of ethics committee application:
2014-06-20
Ethics committee number:
130/14
Vote of the Ethics Committee:
Approved
Date of the vote:
2014-09-11

Further identification numbers

Other primary registry ID:
No Entry
EudraCT Number:
No Entry
UTN (Universal Trial Number):
No Entry
EUDAMED Number:
No Entry

IPD - Individual Participant Data

Do you plan to make participant-related data (IPD) available to other researchers in an anonymized form?:
No Entry
IPD Sharing Plan:
No Entry

Study protocol and other study documents

Publication of study results

Planned publication:
No Entry
Publikationen/Studienergebnisse:
The intervention manuals and materials, and the used questionnaires are accessible via the Bern Open Repository and Information System (BORIS, University of Bern)
All publications are accessible via the Bern Open Repository and Information System (BORIS, University of Bern)
Date of first publication of study results:
No Entry
DRKS entry published for the first time with results:
No Entry

Basic reporting

Basic Reporting / Results tables:
No Entry
Brief summary of results:
No Entry