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Study With an Innovative Equipment to Monitor and Control SALT During Cooking

Not Applicable
Conditions
Hypertension
Salt; Excess
Interventions
Device: SALT CONTROL H equipment to control and monitor salt during cooking process
Registration Number
NCT03974477
Lead Sponsor
Universidade do Porto
Brief Summary

In this study, the researchers will evaluate the efficacy of an intervention using the SALT CONTROL H instrument (an innovative equipment to monitor and control salt) in workers at the University of Porto to reduce dietary salt intake. This is a randomized clinical trial with intervention conducted according to good clinical practice guidelines.

The researchers will randomize 260 workers who meet the eligibility criteria and are enrolled in occupational health appointments. Prior to the intervention, the informed consent of the participants will be obtained and those who agree to participate will be allocated randomly in one of the two arms of the study (control or intervention), with balance of baseline characteristics (sex and hypertension).

The intervention will last for 8 weeks, an individual session of presentation of SALT CONTROL H will be carried out, with explanation of how the equipment works in the culinary preparation with an adequate salt content, will be used an illustrative video and recipes with an adequate salt content; use of SALT CONTROL H at home by the participant to control the use of salt during the cooking process; supervision and enhancement of the use of equipment; daily occurrence log; and the application of a satisfaction questionnaire on the use of SALT CONTROL H. A leaflet will also be delivered about "The new Food Wheel, a guide to the daily food choice!".

Control Group: No intervention will be carried out except the provision of a leaflet on "The new Food Wheel, a guide to the daily food choice!" to the participants.

Baseline, at the 4th and 8th intervention weeks, and 6 months after intervention analysis will cover the following domains: urinary sodium excretion corresponding to a 24 hour urine collection as a proxy for salt intake; 24-hour urinary potassium excretion, sodium:potassium ratio, systolic and diastolic blood pressure, and anthropometric measurements. Urine samples will be collected according to standardized procedures and analyzed by a certified laboratory. Secondary data such as satisfaction questionnaire, daily use of equipment, iodine analysis of salt used and excreted in urine 24h, hydration status, analysis of quality of life and quality of diet will also be analyzed, as well as intestinal microbiota.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
260
Inclusion Criteria
  • Adults (> 18 years)
  • Eat frequently cooked meals at home (> 4 days a week, of which at least 3 Sundays / month)
  • Have an occupational health appoitments at São João Hospital
  • Reported motivation to control salt consumption
Exclusion Criteria
  • Pregnant
  • Subjects with kidney disease,
  • Subjects with active infection with an impact on renal function,
  • Subjects with urinary incontinence,
  • Subjects with acute coronary syndrome,
  • Subjects with severe liver disease;
  • Subjects with heart failure;
  • Subjects who do not use salt for cooking;
  • Subjects with hypotension;
  • Subjects that work at Faculty that are the Sponsor of the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionSALT CONTROL H equipment to control and monitor salt during cooking processThe intervention will last for 8 weeks, an individual session of presentation of SALT CONTROL H will be carried out, with explanation of how the equipment works in the culinary preparation with an adequate salt content (will be used an illustrative video and recipes with an adequate salt content); use of SALT CONTROL H at home by the participant to control the use of salt during the cooking process; supervision and enhancement of the use of equipment; daily occurrence log; and the application of a satisfaction questionnaire on the use of SALT CONTROL H. A leaflet will also be delivered about "The new Food Wheel, a guide to the daily food choice!".
Primary Outcome Measures
NameTimeMethod
Change from Baseline 24h urinary sodium excretion at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Sodium excretion as a proxy of dietary salt intake

Secondary Outcome Measures
NameTimeMethod
Change from Baseline Perception of quality of life at during and after interventionBaseline, at 8th intervention week, and 6 months after intervention

Questionnaire WHOQOL-BREF, results from 0 to 100, higher values represent better perception of quality of life

Change from Baseline Knowledges, attitudes and behaviours about salt at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Questionnaire on Knowledge, Attitudes, Behavior toward Dietary Salt and Health from PAHO (n and %)

Change from Baseline Height at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Height in meters

Change from Baseline Extra and intra cellular water at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Extra and intra cellular water (in kg)

Change from Baseline Systolic Blood Pressure at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Systolic blood pressure

Change from Baseline Diastolic Blood Pressure at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Diastolic blood pressure

Change from Baseline Hydration Status at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

urinary osmolality (mOsm/kg)

Change from Baseline Intestinal Microbiota at after interventionBaseline and at 8th intervention week

OTU (operational taxonomy unit) analysis (%)

Change from Baseline 24h urinary potassium excretion at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Urinary potassium excretion as a proxy of dietary potassium intake

Change from Baseline Culinary competences at during and after interventionBaseline, at 8th intervention week, and 6 months after intervention

Questionnaire, questions scales from 1 to 6 according to culinary competences, higher values represent better culinary competences

Change from Baseline Diet Quality at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

HDI (Healthy Diet Indicator), HDI-2015 was calculated as the sum of 7 components (range 0-7) and was classified as follows: high adherence (met 6-7 components), moderate adherence (met 4-5 components), and low adherence (met 0-3 components)

Change from Baseline Fat Mass and Fat Free Mass at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Fat mass (in kg), Fat free mass (in kg)

Change from Baseline Basal Metabolic Rate at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Basal metabolic rate (in kcal)

Change from Baseline Weight at during and after interventionBaseline, at the 4th and 8th intervention weeks, and 6 months after intervention

Weight in kilograms

Trial Locations

Locations (1)

Carla Gonçalves

🇵🇹

Porto, Portugal

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