- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07512440
Mindfulness and Sustainable Food Choices.
March 31, 2026 updated by: University of Turin, Italy
MindFOODness: Exploring the Impact of Mindfulness on Sustainable Food Choices. A Randomized Controlled Pilot Trial
The goal of this randomized controlled clinical trial is to determine whether a mindfulness-based intervention, in addition to nutritional education, improves healthy and sustainable eating habits in 53 young adults aged 18 to 35 years with low adherence to a sustainable diet.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
50
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Torino
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Torino, Torino, Italy, 10126
- University of Torino
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Aged 18 to 35 years;
- Low adherence to a sustainable diet, defined as a MedQ-Sus score ≤ 3.0;
- Body mass index (BMI) between 18.0 and 29.9 kg/m²;
- Able to provide written informed consent;
- Generally healthy volunteers;
- Omnivorous diet;
- No current or past history of eating disorders;
- Not pregnant and not planning pregnancy during the study period;
- Personally responsible for making food-related decisions.
Exclusion Criteria:
- MedQ-Sus score ≥ 3.1;
- BMI < 18.0 or > 29.9 kg/m²;
- Unable to provide informed consent;
- Dietary restrictions;
- Allergy or intolerance to the tested food.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mindfulness + Nutritional Education
Participants in the experimental group will attend two 1-hour online nutritional education sessions delivered over two consecutive weeks.
In addition, they will participate in a structured online mindfulness program consisting of four 2-hour sessions delivered once weekly for four weeks.
Dietary habits, anthropometric measures, and psychological variables will be assessed at baseline and upon completion of the intervention.
|
The mindfulness-based intervention consists of a structured online program delivered over four weeks.
Participants attend four 2-hour group sessions conducted once weekly.
The program includes guided mindfulness practices, experiential exercises, and group discussions aimed at increasing awareness of eating behaviors, emotional triggers, and food-related decision-making.
The nutritional education intervention consists of two 1-hour online sessions delivered over two separate weeks.
The sessions are based on the EAT-Lancet dietary recommendations for healthy and sustainable eating and provide evidence-based guidance on food choices and dietary patterns consistent with environmental sustainability and health promotion
|
|
Other: Nutritional Education
Participants in the control group will attend two 1-hour online nutritional education sessions delivered over two separate weeks.
The sessions are based on the EAT-Lancet dietary recommendations for healthy and sustainable eating.
Dietary habits, anthropometric measures, and psychological variables will be assessed at baseline and upon completion of the intervention.
|
The nutritional education intervention consists of two 1-hour online sessions delivered over two separate weeks.
The sessions are based on the EAT-Lancet dietary recommendations for healthy and sustainable eating and provide evidence-based guidance on food choices and dietary patterns consistent with environmental sustainability and health promotion
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in adherence to the EAT-Lancet Diet
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
Change in adherence to a healthy and sustainable dietary pattern, assessed using the EAT-Lancet Index.
The index ranges from 0 to 42, with higher scores indicating greater adherence to the EAT-Lancet dietary recommendations.
The total score is derived from 14 dietary components, each scored from 0 to 3. Adherence categories are defined as follows: ≤13 (low adherence), 14-16, 17-19, 20-22, and ≥23 (high adherence).
|
Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in MedQ-Sus score
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
Change in Sustainable diet adherence assessed using the Mediterranean Diet Quality Index for Sustainability (MedQ-Sus; range: 0-8), with higher scores indicating greater adherence to a sustainable diet.
|
Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
|
Change in body weight and body mass index (BMI)
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in body weight measured in kilograms (kg) and in BMI calculated as weight (kg)/height (m²)
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Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in Mindfulness
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in mindfulness (awareness) assessed using the Awareness subscale of the Philadelphia Mindfulness Scale.
Scores range from 10 to 50, with higher scores indicating greater awareness of the present momen.
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Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
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Change in mindful eating behaviors
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in mindful eating (awareness) assessed using the awareness subscale of the Mindful Eating Questionnaire.
Mean scores range from 1 to 4, with higher scores indicating greater awareness of how food affects sensory experiences and internal states.
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Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
|
Change in Psychological distress
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in depression symptoms assessed using the depression subscale of the Depression Anxiety Stress Scales-21 (DASS-21).
Scores range from 0 to 42, with higher scores indicating greater symptom severity.
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Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
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Change in sleep quality
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in sleep quality assessed using the Mini Sleep Questionnaire.
Total scores range from 10 to 70, with higher scores indicating poorer sleep quality.
|
Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
|
Change in Mindfulness
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in Mindfulness (acceptance) assessed using the Acceptance subscale of the Philadelphia Mindfulness Scale.
Scores range from 10 to 50, with higher scores indicating greater acceptance (non-judgmental attitude toward experience).
|
Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
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Change in Mindfulness
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in mindful eating (recognition) assessed using the recognition subscale of the Mindful Eating Questionnaire.
Mean scores range from 1 to 4, with higher scores indicating greater ability to recognize hunger, satiety, and cues that lead to eating beyond physiological needs.
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Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
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Change in Psychological distress
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in anxiety symptoms assessed using the Anxiety subscale of the DASS-21.
Scores range from 0 to 42, with higher scores indicating greater symptom severity.
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Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
|
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Change in Psychological distress
Time Frame: Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Change in stress symptoms assessed using the stress subscale of the DASS-21.
Scores range from 0 to 42, with higher scores indicating greater symptom severity.
|
Baseline, 4 weeks and 8 weeks after the end of the nutritional education sessions
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 14, 2024
Primary Completion (Actual)
July 11, 2025
Study Completion (Actual)
July 11, 2025
Study Registration Dates
First Submitted
March 23, 2026
First Submitted That Met QC Criteria
March 31, 2026
First Posted (Actual)
April 6, 2026
Study Record Updates
Last Update Posted (Actual)
April 6, 2026
Last Update Submitted That Met QC Criteria
March 31, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- MindFood
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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