Food for Mind - Intervention in the Treatment of Depression
Food for Mind - Group-based Behavioral Nutrition Intervention in the Treatment of Depression
Aims. The main aim of the study is to explore whether Food for Mind - Group-based behavioral nutrition intervention alleviates depression symptoms. Furthermore, we aim to investigate, whether the intervention improves the quality of diet, eating habits, quality of life, ability to work and to study its cost-effectiveness.
In collaboration with 11 public and private health care service providers in cities of Kuopio and Siilinjärvi in Northern Savo, Finland.
Participants. The total number of subjects will be 144 based on power calculations. The calculation is based on the clinical decline of seven points assessed by the Center for Epidemiologic Studies Depression (CES-D) Scale. Participants sign an informed consent form to participate Food for Mind - intervention.
Study design.
In this randomized controlled clinical trial subjects are randomized into two parallel groups: Food for Mind -behavioral nutrition intervention group (n=72) and Group to bring Good Mood -control group (n=72).
The intervention consists of behavioral nutrition counselling (5 times 1½ h and 1 time 3 h) and the control group (befriending group) (n=72) (5 times 1½ h and 1 time 3 h). Thus, in the befriending group the same visit schedule and length without any nutrition counselling is used. The befriending group consists of discussion of neutral topics, like hobbies, music, sports, and doing together. Both groups continue to have their normal depression care in the health care.
Enrollment and treatment will take about four years, and follow-up will last about one year.
The Northern Savo Hospital District Committee on Research Ethics gave its consent to the study protocol.
Methods. All questionnaires are validated. CES-D -depression scale, Seasonal Pattern Assessment Questionnaire, The Diet Quality Index (IDQ), Diet frequency -questionnaire, Eating competence -questionnaire (ecSI 2.0), The Three Factor Eating Questionnaire, Ability to work and function -questionnaires, Assessment of Quality of Life (AQoL)-8D (8 dimensions) -questionnaire, Treatment expectancy -questionnaire, Acceptability -questioinnaire.
In addition, body composition measurement and cost-effectiveness analyses to evaluate the health outcomes in relation to resource utilization and costs in Food for Mind -intervention.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Food for Mind -intervention group - topics of small group meetings
- Getting to know each other and forming a group.
- Overall quality of diet and meal rhythm, shifting thoughts to changing of wishes.
- Nutrition and depression based on the evidence based studies
- Mindful Eating - practical Food for Mind cooking class and eating meal together applying mindful eating
- Food for Mind - getting to know a selection of Food for Mind -food items available in the grocery store.
- Tools for the future: discovering and ensuring your own tools for success to put into action.
Participants in the Food for Mind -intervention group will get for every group meeting optional home exercises consisting of observing their own food habits and bringing "food for mind" items on their meal plan. As a social support, participants can share their own experiences and findings via WhatsApp (Whats Application) messenger -mobile application. The WhatsApp messenger-mobile application is used during the intervention and ten months after it.
The behavioral nutrition counselling is theory-based, i.e. solution focused theory (SFT) and self -determination theory. SFT places responsibility for change in the hands of subjects by using empowering language and recognizing them as skilled in matters of self-care. Subjects have strengths, resources, and coping skills that drive change while generating optimism and hope. Use of basic counseling skills, such as attending and listening, genuineness, empathy, positive regard and reflection, provide the foundation upon which SFT is practised.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Outi M Nuutinen, PhD
- Phone Number: +358 50 4691779
- Email: Outi.Nuutinen@uef.fi
Study Contact Backup
- Name: Johanna A Roponen, MSci, RD
- Phone Number: +358 44 245 1211
- Email: ruokaamielelle@uef.fi
Study Locations
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Northern Savo
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Kuopio, Northern Savo, Finland, 70600
- Recruiting
- Psychiatric Centre of Kuopio
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Age 20 - 65 years
- Customer Relationship of Kuopio Psychiatric Center or City of Kuopio: Individually tailored treatment and rehabilitation plan
- ICD-10 (International Classification of Diseases 10th Revision): Depression Diagnosis (F32-F33, F34.1)
- The treatment (medication and / or psychotherapy) has continued unchanged for at least 2 weeks time before randomization
- Willingness to participate in group-based intervention for 8 weeks: 6 group sessions (5 x 1½h and 1 x 3h)
Exclusion Criteria:
- General illness that is clinically unstable and which can be aggravated by intervention
- Pregnancy
- Severe food allergy, intolerance or food aversion
- Participation at the same time, such as other nutrition or exercise intervention
- Primary diagnosis include personality disorder, severe eating disorder and / or substance abuse.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Food for Mind -intervention group
Nutrition counselling + peer support
|
Behavioral nutrition counselling and peer support, delivered in small groups.
Includes six sessions extending over 8 weeks, with participatory activities facilitated by a nutrition therapist.
|
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Active Comparator: Befriending group -control group
Social activation + peer support
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Social activation and peer support, delivered in small groups.
Includes six sessions extending over 8 weeks, with participatory activities facilitated by group leader.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline Depressive Symptomatology at eight weeks, 6 months and 12 months.
Time Frame: 12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
Depressive symptomatology measured with the Center for Epidemiologic Studies (CES-D) scale at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group. The scale has 20 items and measures symptoms of depression. Each item is scored from 0 (zero) to 3 points. The total score ranges from 0 (zero) to 60 points.Higher values of the total score represent a worse outcome.Four of the items (#4, #8, #12, #16) are reversed before calculating the total score. The total score is calculated as follows: the answers to the items are summed, the sum is divided by the number of scored items, and this value is multiplied by 20. If the answers are missing to more than five items, the total score will not be calculated. |
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline Diet Quality at eight weeks, 6 months and 12 months.
Time Frame: 12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
The Diet Quality measured with the Diet Quality Index (IDQ) at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
|
Change from baseline Diet Frequency at eight weeks, 6 months and 12 months.
Time Frame: 12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
The Diet Frequency measured with the Diet frequency -questionnaire at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
|
Change from baseline Eating Competence at eight weeks, 6 months and 12 months.
Time Frame: 12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
Eating Competence measured with the Eating competence -questionnaire (ecSI 2.0) at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
|
Change from baseline Eating Behavior at eight weeks, 6 months and 12 months.
Time Frame: 12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
Eating Behavior measured with The Three Factor Eating Questionnaire at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
|
Change from baseline Ability to Work and Function at eight weeks, 6 months and 12 months.
Time Frame: 12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
Ability to Work and Function measured with the Ability to work and function -questionnaires at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
|
Change from baseline Quality of Life at eight weeks, 6 months and 12 months.
Time Frame: 12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
The Quality of Life measured with the AQoL-8D -questionnaire at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change from baseline body weight at eight weeks, 6 months and 12 months.
Time Frame: 12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
|
Body weight measured by body composition analyzer (InBody720) at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
|
|
Change from baseline fat mass at eight weeks, 6 months and 12 months.
Time Frame: 12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
|
Fat mass measured by body composition analyzer (InBody720) at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
|
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Change from baseline fat free mass at eight weeks, 6 months and 12 months.
Time Frame: 12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
|
Fat free mass measured by body composition analyzer (InBody720) at eight weeks, 6 months and 12 months after patient recruitment compared to the social support befriending group.
|
12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Outi M Nuutinen, PhD, Visiting researcher at the unit of Clinical Nutrition, UEF
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- FoMi
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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