Food for Mind - Intervention in the Treatment of Depression
Primary Purpose
Depression
Status
Recruiting
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Nutrition counselling + peer support
Social activation + peer support
Sponsored by
About this trial
This is an interventional other trial for Depression
Eligibility Criteria
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.
Sites / Locations
- Psychiatric Centre of KuopioRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Food for Mind -intervention group
Befriending group -control group
Arm Description
Nutrition counselling + peer support
Social activation + peer support
Outcomes
Primary Outcome Measures
Change from baseline Depressive Symptomatology at eight weeks, 6 months and 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.
Secondary Outcome Measures
Change from baseline Diet Quality at eight weeks, 6 months and 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.
Change from baseline Diet Frequency at eight weeks, 6 months and 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.
Change from baseline Eating Competence at eight weeks, 6 months and 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.
Change from baseline Eating Behavior at eight weeks, 6 months and 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.
Change from baseline Ability to Work and Function at eight weeks, 6 months and 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.
Change from baseline Quality of Life at eight weeks, 6 months and 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.
Full Information
NCT ID
NCT03904771
First Posted
December 19, 2018
Last Updated
November 16, 2022
Sponsor
University of Eastern Finland
Collaborators
Social Insurance Institution, Finland, Finnish Cultural Foundation
1. Study Identification
Unique Protocol Identification Number
NCT03904771
Brief Title
Food for Mind - Intervention in the Treatment of Depression
Official Title
Food for Mind - Group-based Behavioral Nutrition Intervention in the Treatment of Depression
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 27, 2017 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Eastern Finland
Collaborators
Social Insurance Institution, Finland, Finnish Cultural Foundation
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
144 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Food for Mind -intervention group
Arm Type
Active Comparator
Arm Description
Nutrition counselling + peer support
Arm Title
Befriending group -control group
Arm Type
Active Comparator
Arm Description
Social activation + peer support
Intervention Type
Behavioral
Intervention Name(s)
Nutrition counselling + peer support
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Social activation + peer support
Intervention Description
Social activation and peer support, delivered in small groups. Includes six sessions extending over 8 weeks, with participatory activities facilitated by group leader.
Primary Outcome Measure Information:
Title
Change from baseline Depressive Symptomatology at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
Secondary Outcome Measure Information:
Title
Change from baseline Diet Quality at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
Title
Change from baseline Diet Frequency at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
Title
Change from baseline Eating Competence at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
Title
Change from baseline Eating Behavior at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
Title
Change from baseline Ability to Work and Function at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
Title
Change from baseline Quality of Life at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: assessed at baseline, at eight weeks, at 6 months and at 12 months.
Other Pre-specified Outcome Measures:
Title
Change from baseline body weight at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
Title
Change from baseline fat mass at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
Title
Change from baseline fat free mass at eight weeks, 6 months and 12 months.
Description
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.
Time Frame
12 months: measured at baseline, at eight weeks, at 6 months and at 12 months.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Outi M Nuutinen, PhD
Phone
+358 50 4691779
Email
Outi.Nuutinen@uef.fi
First Name & Middle Initial & Last Name or Official Title & Degree
Johanna A Roponen, MSci, RD
Phone
+358 44 245 1211
Email
ruokaamielelle@uef.fi
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Outi M Nuutinen, PhD
Organizational Affiliation
Visiting researcher at the unit of Clinical Nutrition, UEF
Official's Role
Principal Investigator
Facility Information:
Facility Name
Psychiatric Centre of Kuopio
City
Kuopio
State/Province
Northern Savo
ZIP/Postal Code
70600
Country
Finland
Individual Site Status
Recruiting
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34001230
Citation
Roponen J, Ruusunen A, Absetz P, Partonen T, Kuvaja-Kollner V, Hujo M, Nuutinen O. Nutrition-focused group intervention with a strength-based counseling approach for people with clinical depression: a study protocol for the Food for Mind randomized controlled trial. Trials. 2021 May 17;22(1):344. doi: 10.1186/s13063-021-05279-5.
Results Reference
derived
Learn more about this trial
Food for Mind - Intervention in the Treatment of Depression
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