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Not yet recruitingNCT06448117Updated Sep 19, 2024

Mind Nutrition Study. Effectiveness of Improving Nutrition on Depressive Symptoms and Work Ability

An interventional study of Mind Nutrition in Depressive Symptoms, Nutrition, Healthy and Quality of Life, sponsored by Satakunta University of Applied Sciences. Not yet recruiting at 1 site in Finland. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2024-09-19.

Sponsored by Satakunta University of Applied Sciences · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Primary completion was expected by Aug 2025, 1 year 1 month ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
125
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this randomized, controlled trial is to examine the effectiveness of dietary counseling on depressive symptoms, work ability, and quality of life in mental health and substance abuse professionals. The main questions it aims to answer are:

  • Whether dietary counseling can lower depressive symptoms and depressive symptoms-related sick leave days and improve work ability among mental health and substance abuse professionals
  • Whether dietary counseling can improve life quality, diet quality, and eating behavior among mental health and substance abuse professionals.

Subjects of the intervention group will participate in five dietary counseling sessions during six months. Participants in the control group do not receive any intervention.

Researchers will compare the intervention and control groups to see if dietary counseling is effective in reducing the risk of depressiveness and depression-related sick leave days and improving work ability, quality of life, and nutritional habits.

Read the detailed description

Background. Depressive disorders are a growing public health concern. Depression is linked to increases in work absenteeism, short-term disability, decreased productivity, and presenteeism and has become a global public health challenge. The association between nutrition and the risk of depressiveness is recognized, but there are no published randomized, controlled whole-diet intervention studies with the main aim of depression prevention. It is essential to investigate the impact of nutrition counseling on symptoms of depression in high-risk groups.

Aims. This Mind Nutrition randomized, controlled trial is part of the Mind Nutrition study that combines the intervention part and a cross-sectional examination that utilizes a separate dataset. The primary aim of the intervention study is to examine whether improving nutrition can (cost-effectively) reduce depressive symptoms and related sick leave and enhance work ability. Secondary aims are to measure the effects of the intervention on diet quality, life quality, and eating behavior, evaluate the attainment of participants' personal goals, and assess the acceptability of the intervention.

Methods. The randomized, controlled trial examines the effectiveness of six-month nutritional counseling on depressive symptoms and work ability among practical and registered nurses and social welfare professionals (n=125) working in the mental health and substance abuse field of the Satakunta wellbeing services county. Half of the participants are randomized into the intervention group and half into the control group. The six-month intervention includes two individual and three group counseling sessions. The control group will not receive any intervention but, instead, continue their habitual diet. The investigators measure the outcomes utilizing questionnaires and three-day food records at baseline and the end of the intervention. Weight and blood pressure will be measured at the same time points.

Discussion. This study will provide nationally and internationally crucial evidence on the effectiveness of nutrition counseling on depressive symptoms, work ability, and quality of life.

02

Conditions studied

  • Depressive Symptoms
  • Nutrition, Healthy
  • Quality of Life
  • Eating Behavior
  • Work-Related Condition

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Keywords

  • Depressive Symptoms
  • Nutrient intake
  • Work ability
  • Quality of Life
  • Randomized, controlled trial
  • Nutritional counseling
03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,641 are open to participants now.

This study's planned enrollment of 125 is above the median of 84 across 6,720 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

This is the only study on the registry with Satakunta University of Applied Sciences as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Aged at least 18 year
  • Adequate Finnish language skills
  • Work-capable
  • Currently employed by Satakunta wellbeing services county for at least 6 months
  • Works in the field of mental health and substance abuse
  • Education either practical nurse, registered nurse, mental health nurse, or Bachelor of Social Services (in Finnish: Sosionomi)
  • Agrees to commit to either of the groups (intervention/control) for 6 months
  • Able to give informed consent.

Exclusion criteria

Exclusion Criteria:

  • Acute mental health symptoms and incapable to work
  • Terminal phase disease or unstable severe chronic disease (consultation of the doctor in charge)
  • Employed for a shorter period than 6 months
  • Has a history of an eating disorder (consultation of the doctor in charge)
  • Center for Epidemiological Studies - Depression (CES-D) score ≥16 and reduced work capacity (presenteeism) (consultation of the medical expert in mental health)
  • Substance abuse based on the AUDIT-C score (consultation of the doctor in charge)
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
125 participants (estimated)

Study arms

  • Experimental
    "Mind Nutrition" Nutritional counseling

    The intervention arm includes five dietary counseling sessions during 6 months.

    Behavioral: Mind Nutrition

  • No intervention
    Control

    The control arm does not include any intervention.

Interventions

  • BehavioralMind Nutrition

    The 6-month nutrition intervention includes two individual and three group dietary counseling sessions. During the first individual meeting, a research dietitian will assess the participants' diet quality and eating habits, and each participant will set personal goals in cooperation with the research dietitian. At the second individual meeting, the attainment of the goals will be evaluated, and potential challenges and solutions discussed. Each group session has its theme and content in the following chronological order: 1. Introduction to the theme and importance of a regular meal frequency 2. Principals of health-promoting diet, mindful eating 3. Successful eating regulation skills, psychology of the long-term lifestyle changes. Additionally, participants receive home assignments and a workbook containing informational material and exercises.

06

What researchers measure

Primary outcomes

  1. Change in depressive symptoms

    Change in depressive symptoms measured with the Center for Epidemiological Studies - Depression (CES-D) questionnaire. It has 20 questions with response options from 0 to 3 points. Possible scores are between 0-60 with higher scores meaning more severe depression symptomology.

    Time frame: 6 months

  2. Change in work ability

    Change in work ability measured with a three-step work ability indicator created by the Finnish Institute for Health and Welfare: "Regardless of whether you are employed or not, please estimate your current work ability." The answer options are coded in three different categories: 1) completely fit for work (2 points), 2) partially unable to work (1 point), and 3) completely unable to work (0 points)."

    Time frame: 6 months

  3. Change in depressive symptoms-related sick leave days

    Change in the number of depressive symptoms-related sick leave days assessed with a structured question.

    Time frame: 6 months

Secondary outcomes

  1. Change in quality of life

    Change in quality of life measured with the World Health Organization Eurohis-QOL (WHO8-EUROHIS) questionnaire. It has eight items with a 5-point response format on a Likert scale. The total score is obtained by summing the eight items and dividing the result by eight, meaning that the possible scores are between 1-5. Higher scores indicate better life quality.

    Time frame: 6 months

  2. Change in dietary habits

    Change in dietary habits assessed with a 163-item Food frequency questionnaire (FFQ) created by the University of Eastern Finland and the Baltic Sea Diet Score derived from the FFQ data. The FFQ comprises nine frequency response options which are multiplied by the portion sizes (grams) to obtain consumption of each listed food item. Average daily food, nutrient, and energy intakes are calculated using the Finnish National Food Composition (Fineli®) database. The Finnish Healthy Diet Index (HDI) score will be derived from the data. Scores range from 0 to 100, with higher scores meaning better diet quality.

    Time frame: 6 months

  3. Change in energy and nutrient intake

    Change in energy and nutrient intake measured with three-day food records utilizing the Eat@Work mobile application by the Satakunta University of Applied Sciences.

    Time frame: 6 months

  4. Change in eating behavior

    Change in Eating behavior assessed by the Three Factor Eating Questionnaire - 18 (TFEQ-18). Its three domains (emotional eating, uncontrolled eating, and cognitive restraint) are measured with 18 questions. Raw scores are scaled to 0-100 points, with higher scores meaning a stronger tendency for each behavior domain.

    Time frame: 6 months

07

Study locations

1 site
  • Satakunta University of Applied Sciences
    Pori, Satakunta 28130, Finland
    • Susanna Kunvik, PhD · Contact · susanna.kunvik@samk.fi · +358447103204
    • Aino Kipfer, MSc · Contact · aino.kipfer@samk.fi · +358505678410
    • Aino Kipfer, MSc · Sub investigator
    • Maarit Hallia, MHC · Sub investigator
    • Minna Kahala, MSc · Sub investigator
    • Jari Kyngäs, PhD · Sub investigator
    • Susanna Kunvik, PhD · Principal investigator
    • Juha Puustinen, PhD · Sub investigator
    • Jyrki Korkeila, PhD · Sub investigator
    • Anu Ruusunen, PhD · Sub investigator
    • Lotta-Emilia Hakkarainen, MBA · Sub investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 19, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06448117
Lead sponsor
Satakunta University of Applied Sciences
Responsible party
Sponsor
First posted
Jun 7, 2024
Start date
Sep 1, 2024 (estimated)
Primary completion
Aug 31, 2025 (estimated)
Completion
Aug 31, 2025 (estimated)
Last update
Sep 19, 2024

Study contacts

Susanna Kunvik, PhD
Contact
susanna.kunvik@samk.fi
+358447103204
Aino Kipfer, MSc
Contact
aino.kipfer@samk.fi
+358505678410
Susanna Kunvik, PhD
principal investigator · Senior Researcher

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is not yet recruiting, as verified in Sep 2024. You cannot join it, but the record below documents what was studied.

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