Feasibility and Acceptability of a Healthy Nordic Diet Intervention in Depressed and Non-depressed Adults

Depression Clinical Trial

Official title:

Feasibility and Acceptability of a Healthy Nordic Diet Intervention for the Treatment of Depression: a Randomized Controlled Pilot Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04731454
• Other study ID #: 2020-03735
• Status: Completed
• Phase: N/A
• Start date: September 15, 2020
• Est. completion date: October 2, 2020

Study information

• Verified date: January 2021
• Source: Örebro University, Sweden
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In the future, we plan to conduct an 8-week diet intervention to investigate whether a healthy Nordic diet improves depression symptoms. The present pilot study tested whether the planned meals and diets were well-liked and accepted by participants (both depressed and non-depressed) in order to ensure that the future diet intervention will be feasible and successful. We also investigated whether any changes in health occurred after 8 days of this diet intervention.

Description:

After providing their written informed consent, participants were randomized to receive either a healthy Nordic diet or a control diet for 8 days. All meals were provided and minimal food preparation was required. Participants picked up their food outside the study kitchen every 3 days. Before and after the intervention, health-related self-rated questionnaires were completed. For every meal during the intervention, participants completed a questionnaire on their perceptions of the meal. Every evening a questionnaire was completed to assess dietary adherence. At the end of the study, a final evaluation questionnaire was completed to assess participants' perceptions of the diet and study as a whole.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: October 2, 2020
• Est. primary completion date: October 2, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• If depressed, a score between 13 and 34 on the Montgomery-Åsberg Depression Rating Scale, self-rated (MADRS-S), indicating mild or moderate depression

Exclusion Criteria:

• A score of 8 or higher (out of a maximum of 12 points) on a brief diet survey (the retired version of the Swedish Food Agency's online Matvanekollen, conducted via phone interview), indicating a relatively healthy habitual diet
• Presence of food allergies, intolerances or sensitivities
• Consuming any form of special diet that excludes certain foods, for example a vegetarian or gluten-free diet
• Suicidality, indicated by a score of 4 or higher on the MADRS-S suicidality question.

Related Conditions & MeSH terms

• Depression
• Depressive Disorder
• Depressive Disorder, Major
• Major Depressive Disorder

Intervention

Other:
• Control Diet (CD)
All food was provided to participants for the duration of the intervention (8 days), including prepared lunches and dinners and ingredients for breakfasts and snacks. A sugar-sweetened juice drink was provided for consumption of one portion per day. Water, milk, coffee, tea and alcohol were consumed as usual.
• Healthy Nordic Diet (ND)
All food was provided to participants for the duration of the intervention (8 days), including prepared lunches and dinners and ingredients for breakfasts and snacks. Water, milk, coffee, tea and alcohol were consumed as usual.

Locations

Country	Name	City	State
Sweden	Örebro University	Örebro	Närke

Sponsors (1)

Lead Sponsor	Collaborator
Örebro University, Sweden

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Median rating of the liking of all meals as assessed by a Likert item (the Hedonic scale)	1=Dislike very much, and 7=Like very much. Median of responses for all meals for each participant calculated first, and then the median of those medians calculated and reported for each diet group.	8 days
Primary	Median rating of the appearance of all meals as assessed by an original Likert item	1=Dislike very much, and 7=Like very much. Median of responses for all meals for each participant calculated first, and then the median of those medians calculated and reported for each diet group.	8 days
Primary	Median rating of the smell of all meals as assessed by an original Likert item	1=Dislike very much, and 7=Like very much. Median of responses for all meals for each participant calculated first, and then the median of those medians calculated and reported for each diet group.	8 days
Primary	Median rating of the extent to which the smell matches the appearance of the meals as assessed by an original Likert item	1=Doesn't match at all, and 5=Matches very well. Median of responses for all meals for each participant calculated first, and then the median of those medians calculated and reported for each diet group.	8 days
Primary	Median rating of the taste intensity of all meals as assessed by a Just About Right (JAR) scale	1=Much too low, 3=Just right, and 5=Much too high. Median of responses for all meals for each participant calculated first, and then the median of those medians calculated and reported for each diet group.	8 days
Primary	Median rating of the portion size of all meals as assessed by a Just About Right (JAR) scale	1=Much too small, 4=Just right, and 7=Much too big. Median of responses for all meals for each participant calculated first, and then the median of those medians calculated and reported for each diet group.	8 days
Primary	Median rating of feelings of fullness after the meals as assessed by an original visual analog scale (VAS)	0=Not at all full, and 100=Have never felt so full. Median of responses for all meals for each participant calculated first, and then the median of those medians calculated and reported for each diet group.	8 days
Primary	Median perception of healthiness of all meals as assessed by an original visual analog scale (VAS)	0=Not at all healthy, and 100=Very healthy. Median of responses for all meals for each participant calculated first, and then the median of those medians calculated and reported for each diet group.	8 days
Primary	Total amount of non-study foods consumed as assessed by self-report on a questionnaire every evening		8 days
Primary	Total amount of non-study drinks consumed as assessed by self-report on a questionnaire every evening		8 days
Primary	Total amount of provided juice drink not consumed as assessed by self-report on a questionnaire every evening.	Applies to the CD group only.	8 days
Primary	Rating of how easy it was to follow the protocol, as assessed by an original Likert item on the final questionnaire	1=It was very hard, and 7=It was very easy	8 days
Primary	Rating of how easy it would be to participate in such a study, with meals recurring every 8 days for 8 weeks (but not having to fill out a questionnaire for the meals)	Assessed by an original Likert item on the final questionnaire where 1=It would be very hard, and 7=It would be very easy	8 days
Secondary	Change in work impairment after 8 days, as calculated from questions of the Work Productivity and Activity Impairment (WPAI) questionnaire	Expressed as percentage impairment, from 0-100%, where higher values indicate greater impairment in work ability	8 days
Secondary	Change in activity impairment after 8 days, as calculated from questions of the Work Productivity and Activity Impairment (WPAI) questionnaire	Expressed as percentage impairment, from 0-100%, where higher values indicate greater impairment in ability to perform daily activities.	8 days
Secondary	Change in gastrointestinal symptom severity after 8 days, as assessed by the total mean score of the Gastrointestinal Symptoms Rating Scale (GSRS) questionnaire	1=no symptoms, 7=very severe symptoms	8 days
Secondary	Change in indigestion symptom severity after 8 days, as assessed by the indigestion sub-score of the Gastrointestinal Symptoms Rating Scale (GSRS) questionnaire	1=no symptoms, 7=very severe symptoms	8 days
Secondary	Change in physical activity level after 8 days, as assessed by the Frändin-Grimby Physical Activity Scale	Score of 1-6, from least to most active	8 days
Secondary	Change in depression severity after 8 days, as assessed by the total score of the Montgomery-Åsberg Depression Rating Scale, self-rated (MADRS-S) questionnaire	Score of 0-54, from least to most severe symptoms	8 days
Secondary	Change in perceived general health status after 8 days, as assessed by the visual analog scale (VAS) question of the EuroQol Health-Related Quality of Life (EQ-5D-5L) questionnaire	0=Worst health imaginable, 100=Best health imaginable	8 days
Secondary	Change in general health after 8 days, as assessed by the summary index value calculated from the questions of the EuroQol Health-Related Quality of Life (EQ-5D-5L) questionnaire	0=health as bad as dead, 1=full health	8 days
Secondary	Self-reported change in health after 8 days, as assessed by a written open-ended response on the final questionnaire	Due to the open-ended, self-reported nature of the responses, they are summarized narratively rather than quantitatively.	8 days
Secondary	Change in body weight after 8 days, as assessed by self-measurement or approximation	Change between self-reported baseline and follow-up body weights calculated.	8 days