Effect of Saffron Extract Supplementation on Emotional Well-being Alterations (SAFFROMFOOD)

Investigation of the Effect of Saffron Extract Supplementation on Emotional Well-being Alterations in Healthy Volunteers: a Randomized, Double-blind, Placebo-controlled Study

This study aims to test whether a saffron extract represents a good candidate to improve emotional well-being in subjects with subclinical symptoms of depression, fatigue, stress or anxiety. Given that mild depression, both subclinical and chronic, was shown to predispose to major clinical depression, early initiation of neuroactive nutrient supplementation may be useful to prevent or counteract the onset of chronic depression.

The main objective of this study is to evaluate the efficacy of nutritional supplementation with saffron extract during 6 weeks in alleviating emotional well-being alterations in healthy adults presenting subclinical symptoms of depressed mood, anxiety, fatigue and/or stress.

The secondary objectives are to assess the impact of saffron extract supplementation on the mood and neurovegetative components of emotional well-being and quality of life, namely:

• depressive and anxious symptoms;
• neurovegetative symptoms (fatigue, sleep quality);
• perceived stress and quality of life.

The exploratory objectives correspond to the biological assays for the evaluation of

• the stress response system (stress hormones);
• the inflammatory status;
• saffron metabolites;
• metabolome.

Study Overview

• Status: Recruiting
• Conditions: Mood Disturbance
• Intervention / Treatment: Dietary supplement: Saffron extract; Dietary supplement: Maltodextrin

• Study Type: Interventional
• Enrollment (Anticipated): 50
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Lucile Capuron, PhD; Phone Number: +33557571233; Email: lucile.capuron@inrae.fr

Study Locations

• France
  • Dijon, France, 21000
    • Recruiting
    • CEN experimental
    • Principal Investigator: Carole PERRIN, MD

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 50 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Healthy volunteers (as determines by medical history and clinical examination);
• Male or female between 18 and 50 years of age;
• Body Mass Index (BMI) 18.5 ≤ BMI < 30 kg/ m2;
• Subject with subclinical symptoms of depressed mood, anxiety, fatigue and/or stress, as determined by the presence of at least 6 or more symptoms of moderate intensity among the 18 symptoms listed in the modified neurotoxicity scale (NRS).
• Subject able and willing to participate to the study by complying with the protocol procedures as confirmed by his dated and signed informed consent form;
• Person affiliated or benefiting from a social security scheme.

Exclusion Criteria:

• Psychiatric comorbidity determined with the Diagnostic and Statistical Manual of Mental Disorders 5 (DSM5) or history of psychiatric illness;
• Neurodegenerative pathology (Alzheimer's disease, Parkinson's disease, dementia);
• Cardio-metabolic diseases (cardiovascular diseases, type 1 or 2 diabetes...);
• Untreated or unstabilised hypertension;
• Severe chronic diseases (cancer, severe chronic pain, HIV, hepatitis, kidney disease, autoimmune diseases, etc.);
• Chronic inflammatory diseases (Crohn's disease, coeliac disease, rheumatoid arthritis, etc.);
• Pathologies likely to act on the Hypothalamus-Pituitary-Adrenal (HPA) axis or the adrenal cortical metabolism (e.g.: Cushing syndrome);
• Untreated and/or unstabilised thyroid diseases (hypo/hyperthyroidism, Graves' disease...);
• Subjects treated during the previous 6 months or being currently treated with psychotropic drugs prescribed and/or recommended for anxiety, depression, sleep disorders and generally for any neurological or psychological type of manifestation.

The same applies to:

• Drugs likely to have direct or indirect effects on psychiatric symptoms, notably regular use of corticoids or steroidal anti-inflammatories (e.g. Betamethasone, Cortivazol, Dexamethasone, Methylprednisolone, Prednisolone, Prednisone, Tetracosactide, Triamcinolone, etc.);
• Any drug treatment aimed at improving or maintaining cognitive functions (e.g. Aricept, Exelon, Reminyl, Ebixa etc.);
• Food supplements during the last 3 months prior to participation in this study.
• Personal or professional event with potential severe impact on the subject's emotional and/or psychological state within the last 8 weeks (e.g. but not limited to: change of job function/position, death of a family member, divorce, surgery, accident, etc.);
• Use of antibiotic treatment (<2 months);
• Recent treatment with non-steroidal anti-inflammatory drugs (<1 month);
• Bariatric surgery;
• Subject with asthma, allergies (allergic rhinitis, atopic dermatitis);
• Any documented or suspected food allergy to any component of the study products.
• Drug dependence (except tobacco);
• Tobacco use of more than 20 cigarettes per day;
• Consumption of large quantities of coffee, tea, chocolate (more than 5 cups of coffee or tea and more than 20 g of dark chocolate per day) or regular daily consumption of herbal infusions with relaxing or hypnotic properties [e.g. chamomile, valerian, passionflower etc];
• Alcohol abuse (maximum 2 drinks per day, maximum 10 drinks per week with several days of abstinence) or recreational drug use based on the participant's declaration;
• Eating disorders: anorexia and bulimia or unstable diet;
• Xerostomia or other conditions that may make saliva collection impossible;
• Subjects working shifts or in extreme conditions (e.g. cold storage);
• Intense physical activity: more than 10 hours per week of intense physical activity, or significant change in physical activity within the last 2 months, or physical activity likely to be modified within the next 6 weeks. Examples of moderate to vigorous physical activity are: carrying heavy loads, playing tennis (singles or doubles), combat sports, "fast" swimming, jogging etc. Walking is not considered a moderate intensity physical activity.
• Subjects whose language skills do not allow them to understand the questionnaires;
• Disability (psychological, visual, psychomotor, linguistic...) likely to compromise to understand and sign the consent form and to complete self-questionnaires during the study.
• Subject participating in another interventional study or being in the exclusion period of a previous clinical trial;
• Subject receiving more than 4500 euros as indemnities for participation in biomedical research within the 12 last months, including indemnities for the present study;
• Women who are pregnant, intend to become pregnant during the study or are breastfeeding.
• Hormonal state that may induce a fluctuating emotional state during the study, such as, postpartum (< 6 months after delivery) and peri-menopause (irregular menstrual cycle, hot flashes, feeling of swelling, breast tension).
• Subjects under legal protection (guardianship, wardship) or deprived from his rights following administrative or judicial decision;

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Saffron extract; Daily, two dietary supplements (Saffron extract) will be taken orally with water, the first one at breakfast and the second one at dinner. Dietary supplements in capsule form	Dietary supplement: Saffron extract; Food supplements are taken during 6 weeks by healthy volunteers
Placebo Comparator: Placebo; Daily, two dietary supplements (Maltodextrin) will be taken orally with water, the first one at breakfast and the second at dinner. Dietary supplements in capsule form	Dietary supplement: Maltodextrin; Food supplements are taken during 6 weeks by healthy volunteers

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in emotional well-being composite score	The primary endpoint is the change from baseline (V1) to 6 weeks (V2) in the composite Z-score of emotional well-being combining three components: depression (BDI score), anxiety (STAI state score) and fatigue (MFI score).	Baseline (V1) and 6 weeks (V2)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in mood	Beck Depression Inventory (score 0-39).	Baseline (V1) and 6 weeks (V2)
Change in anxiety	State-Trait Anxiety Inventory (score 20-80).	Baseline (V1) and 6 weeks (V2)
Change in stress	Visual analog scale for stress (score 0 to 10).	Baseline (V1) and 6 weeks (V2)
Change in fatigue	Multidimensional Fatigue Inventory (MFI) (score 20-100).	Baseline (V1) and 6 weeks (V2)
Change in sleep quality	The Pittsburgh Sleep Quality Index (PSQI) (score 0 to 21).	Baseline (V1) and 6 weeks (V2)
Change in neurovegetative symptomatology	Neurotoxic rating scale (NRS) (score 0 to 152).	Baseline (V1) and 6 weeks (V2)
Change in quality of life	Medical Outcome Study Short Form 12 (SF-12) (score 0 to 100).	Baseline (V1) and 6 weeks (V2)
Change in dietary intake	Subjects will complete a food diary in which they will register all the food and drinks consumed during 3 defined days (two weekdays and one weekend day). The Programme national nutrition santé (PNNS) questionnaire is a non-quantitative food frequency questionnaire. The 12 items are based on the recommendations of the French National Nutrition and Health.	Baseline (V1) and 6 weeks (V2)
Change in stress response system	Salivary cortisol as a measure of the stress response system.	Baseline (V1) and 6 weeks (V2)
Change in inflammatory markers	Blood levels of acute phase proteins and cytokines.	Baseline (V1) and 6 weeks (V2)
Change in oxidative stress	Blood oxidative stress markers such as malondialdehyde (MDA), total antioxidant capacity (TCA) and superoxide dismutase (SOD) levels.	Baseline (V1) and 6 weeks (V2)
Change in saffron metabolites	Blood and urine polyphenols and carotenoids levels.	Baseline (V1) and 6 weeks (V2)
Change in metabolome	Untargeted metabolomics analysis in blood and urine samples using nuclear magnetic resonance (NMR) and/or liquid chromatography-mass spectrometry (LC-MS).	Baseline (V1) and 6 weeks (V2)
Change in lipid profile	Lipids profile in red blood cells.	Baseline (V1) and 6 weeks (V2)

Collaborators and Investigators

• Sponsor: Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement
• Investigators: Study Director: Lucile Capuron, PhD, INRAE-Laboratory of Nutrition And Integrative Neurobiology (NutriNeuro Lab)

Study record dates

Study Major Dates

• Study Start (Actual): December 8, 2022
• Primary Completion (Anticipated): December 1, 2023
• Study Completion (Anticipated): December 1, 2023

Study Registration Dates

• First Submitted: December 21, 2022
• First Submitted That Met QC Criteria: January 9, 2023
• First Posted (Estimate): January 19, 2023

Study Record Updates

• Last Update Posted (Estimate): January 19, 2023
• Last Update Submitted That Met QC Criteria: January 9, 2023
• Last Verified: January 1, 2023

More Information

Terms related to this study

• Keywords: Inflammation; Anxiety; Fatigue; Sleep quality; Depressive Symptoms; Saffron extract; Emotional wellbeing
• Other Study ID Numbers: 2022-A01556-37

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