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Effects of Nutrients Supplementation in Antidepressant Treated Depressive Disorder Patients

Primary Purpose

Depressive Disorder, Major

Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
LF/Erinacine A-enriched Hericium/Plain chocolate + antidepressant(s)
Sponsored by
National Cheng-Kung University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder, Major focused on measuring Major depressive disorder, Supplement nutrients, Antidepressants

Eligibility Criteria

20 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Major depressive disorder (MDD) outpatients meet DSM- criteria
  • Hamilton Rating Scale for Depression (HAM-D) ≥ 7
  • Start to receive fluoxetine or venlafaxine or those who have received the SSRI or SNRI antidepressants

Exclusion Criteria:

  • (A) had DSM-5 diagnosis for substance abuse within the past three months;
  • (B) had taken monoamine oxidase inhibitors;
  • (C) had an organic mental disorder, mental retardation, dementia, or other diagnosed neurological illness;
  • (D) had a surgical condition or a major physical illness;
  • (E) pregnant or breast-feeding.

Sites / Locations

  • National Cheng-Kung UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

Placebo Comparator

Arm Label

LF chocolate + antidepressant(s)

Erinacine A-enriched Hericium chocolate + antidepressant(s)

Plain chocolate + antidepressant(s)

Arm Description

Participants with LF chocolate add-on to their antidepressants regimen.

Participants with Erinacine A-enriched Hericium chocolate add-on to their antidepressants regimen.

Participants with plain chocolate add-on to their antidepressants regimen.

Outcomes

Primary Outcome Measures

Change in participant's Hamilton Rating Scale for Depression (HAM-D) score
Depressive symptom rating; 21 items int total, eight items are scored on a 5-point scale, ranging from 0 = not present to 4 = severe, while nine are scored from 0-2; [higher scores denote worse symptoms/signs of depression]
Change in participant's BW(kg), Height(cm), Waist circumference(cm), BMI (kg/m2)
Metabolic indices; BW (to the nearest 0.1 kg), height (to the nearest 0.1 cm), and waist circumference (to the nearest 0.1 cm), weight and height will be combined to report BMI in kg/m^2
Change in participant's Glucose profiles
Metabolic indices; HbA1c(%)+Fasting plasma glucose (mg/dl)+Fasting serum insulin concentrations (uIU/ml)+Homeostasis model assessment-estimated insulin resistance (HOMA-IR) index+Homeostasis model of assessment for pancreatic β-cell secretory function (HOMA-β) {HOMA- IR= [fasting plasma insulin level (uIn/ml)*fasting plasma glucose level (mg/dl)/405]; HOMA- IR ≥2.5 => Insulin resistance (+)} {HOMA-β= (360× fasting serum insulin [uIn/ml]) / (fasting plasma glucose [mg/dL] -63)}
Change in participant's Fasting serum leptin level (ng/mL)
Metabolic indices
Change in participant's Fasting serum lipid profiles
Metabolic indices; including Fasting total cholesterol(mg/dL), High density lipoprotein (HDL) cholesterol(mg/dL), Low-density lipoprotein (LDL) cholesterol(mg/dL), Triglyceride (TG) concentration(mg/dL)
Change in participant's Cortisol(ug/dL) level
Metabolic indices
Change in participant's C-peptide(ng/dL)
Metabolic indices
Change in participant's Inflammatory cytokines levels
Metabolic indices; Fasting plasma C-reactive protein (CRP) level (pg/mL) + Oxytocin(pg/mL) + Leptin(mg/mL)
Change in participants's Quality of life scale (QOLs) scores [WHOQOL-BREF]
Psychosocial variables as environment factors; Quality of Life Scale developed through the World Health Organization (WHOQOL-BREF) & Health-Related Quality of Life (HRQOL) questionnaires will be used as assessment tools WHOQOL-BREF: 4 domains will be assessed, consists of 1. Physical Health 2. Psychological 3. Social Relationship 4. Environment; [higher scores in each domains denote higher quality of life]
Change in participants's Quality of life scale (QOLs) scores [HRQOL]
Psychosocial variables as environment factors; Quality of Life Scale developed through the World Health Organization (WHOQOL-BREF) & Health-Related Quality of Life (HRQOL) questionnaires will be used as assessment tools HRQOL: 4 domains will be assessed, consists of 1. Physical Health 2. Psychological 3. Level of independence 4. Social Relationship [higher scores in each domains denote higher quality of life]
Change in participant's Cognitive performance
Continuous Performance Test (CPT)[visual information processing & attentive capacity], Finger Tapping Test (FPT), Wisconsin Card-Sorting Test (WCST)
Change in participant's Social cognitive functional performance
Mayer-Salovey-Caruso emotional Intelligence Test (MSCEIT) scores; perceiving + facilitating + understanding + managing emotion
Change in participant's Microbiota profiles
Fecal samples; Types of microorganisms + no. of colonies (colony-forming unit, CFU)

Secondary Outcome Measures

Full Information

First Posted
November 19, 2019
Last Updated
September 8, 2021
Sponsor
National Cheng-Kung University Hospital
Collaborators
Grape King Bio Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT04179006
Brief Title
Effects of Nutrients Supplementation in Antidepressant Treated Depressive Disorder Patients
Official Title
Effects of Nutrients Supplementation in Antidepressant Treated Depressive Disorder Patients
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Recruiting
Study Start Date
November 14, 2019 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Cheng-Kung University Hospital
Collaborators
Grape King Bio Ltd.

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
This is a randomized, double-blind, placebo-controlled to evaluate the potential role of nutrients supplementation (LF chocolate /Erinacine A-enriched Hericium Erinaceus chocolate) on the therapeutic efficacy of antidepressants in major depressive disorder(MDD). 120 subjects who meet all the inclusion and exclusion criteria will be randomized into three categories, receiving 3 pieces of supplement nutrients-added or plain chocolates per day for a period of 24 weeks in total. The three categories are as follow: LF chocolate Erinacine A-enriched Hericium Erinaceus chocolate Plain chocolate without any supplementary nutrients added (placebo group) These MDD patients will continue their antidepressant regimen throughout the study. Symptom rating, blood samples for antidepressant-related/depressive disorder-related genome profiles identification, as well as for biomarkers assessment for metabolic indices, questionnaires and tests for psychosocial variables identification and patient's cognitive and social cognitive function or performance determination, will be carried out before and at certain time points within the 24-week tracking period. Patient's fecal samples will be acquired to recognize and to distinguish the alterations of these MDD patients microbiota profiles over the 24-week period.
Detailed Description
Major depressive disorder (MDD) is a common, severe, and often life-threatening illness that involves the body, mood, and thoughts. Recent reports suggested that immune dysfunction could be linked with cognitive impairment and metabolic comorbidities, and accumulating evidence suggested that the regulation of the microbiota- gut-brain axis has been shown to impact inflammation and to affect brain function. This randomized, double-blind, placebo-controlled is to evaluate the potential role of nutrients supplementation (LF chocolate /Erinacine A-enriched Hericium Erinaceus chocolate) on the therapeutic efficacy of antidepressants in major depressive disorder(MDD). 120 MDD outpatients (aged 20-70 years) from the National Cheng Kung University Hospital who meet the Diagnostic and Statistical Manual of mental disorders, Fifth Edition (DSM-5) and Hamilton Rating Scale for Depression (HAMD) scores ≥ 7, receiving fluoxetine or venlafaxine so as SSRI or SNRI antidepressants will be enrolled. Subjects who meet all the inclusion and exclusion criteria will be randomized into three categories, with 40 subjects each, receiving 3 pieces of supplement nutrients-added or plain chocolates (placebo) manufactured by GRAPE KING BIO LTD per day for a period of 24 weeks in total. The three categories are as follow: LF chocolate Erinacine A-enriched Hericium Erinaceus chocolate Plain chocolate without any supplementary nutrients added (placebo group) These MDD patients will continue their antidepressant regimen throughout the study. Follow-up visits will be arranged at week no. 0, 2, 4, 8, 12, 16, 20 and 24, in which week no. 0, 4, 12 and 24 will be the four most important re-visit timing. Various assessments or tests will be arranged in these 24-week period. Symptom rating with 17-item Hamilton Rating Scale for Depression (HAM-D) by psychiatrist will be done at every visits. Blood samples for antidepressant-related/depressive disorder-related genome profiles identification, as well as for biomarkers assessment for metabolic indices, will be obtained at week no. 0, 4, 12 and 24. Questionnaires aimed for psychosocial variables (environmental factors) identification including social support scales (SSS), quality of life scale (QOLs) and Recent life changes questionnaire (RCLQ) will be self-answered by patients. Continuous Performance Test (CPT), finger-Tapping Test (FPT) and Wisconsin Card Sorting Test (WCST) will be utilized to evaluate their cognitive performance. Mayer-Salovey-Caruso emotional Intelligent Test (MSCEIT) will help in social cognitive function assessment. Patient's fecal samples will be acquired at week no. 0, 4, 12 and 24 to recognize and to distinguish the alterations in MDD patients microbiota profiles.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Disorder, Major
Keywords
Major depressive disorder, Supplement nutrients, Antidepressants

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
LF chocolate + antidepressant(s)
Arm Type
Active Comparator
Arm Description
Participants with LF chocolate add-on to their antidepressants regimen.
Arm Title
Erinacine A-enriched Hericium chocolate + antidepressant(s)
Arm Type
Active Comparator
Arm Description
Participants with Erinacine A-enriched Hericium chocolate add-on to their antidepressants regimen.
Arm Title
Plain chocolate + antidepressant(s)
Arm Type
Placebo Comparator
Arm Description
Participants with plain chocolate add-on to their antidepressants regimen.
Intervention Type
Dietary Supplement
Intervention Name(s)
LF/Erinacine A-enriched Hericium/Plain chocolate + antidepressant(s)
Intervention Description
3 pieces per day
Primary Outcome Measure Information:
Title
Change in participant's Hamilton Rating Scale for Depression (HAM-D) score
Description
Depressive symptom rating; 21 items int total, eight items are scored on a 5-point scale, ranging from 0 = not present to 4 = severe, while nine are scored from 0-2; [higher scores denote worse symptoms/signs of depression]
Time Frame
week no. 0, 2, 4, 8, 12, 16, 20, 24
Title
Change in participant's BW(kg), Height(cm), Waist circumference(cm), BMI (kg/m2)
Description
Metabolic indices; BW (to the nearest 0.1 kg), height (to the nearest 0.1 cm), and waist circumference (to the nearest 0.1 cm), weight and height will be combined to report BMI in kg/m^2
Time Frame
week no. 0, 2, 4, 8, 12, 16, 20, 24
Title
Change in participant's Glucose profiles
Description
Metabolic indices; HbA1c(%)+Fasting plasma glucose (mg/dl)+Fasting serum insulin concentrations (uIU/ml)+Homeostasis model assessment-estimated insulin resistance (HOMA-IR) index+Homeostasis model of assessment for pancreatic β-cell secretory function (HOMA-β) {HOMA- IR= [fasting plasma insulin level (uIn/ml)*fasting plasma glucose level (mg/dl)/405]; HOMA- IR ≥2.5 => Insulin resistance (+)} {HOMA-β= (360× fasting serum insulin [uIn/ml]) / (fasting plasma glucose [mg/dL] -63)}
Time Frame
week no. 0, 4, 12, 24
Title
Change in participant's Fasting serum leptin level (ng/mL)
Description
Metabolic indices
Time Frame
week no. 0, 4, 12, 24
Title
Change in participant's Fasting serum lipid profiles
Description
Metabolic indices; including Fasting total cholesterol(mg/dL), High density lipoprotein (HDL) cholesterol(mg/dL), Low-density lipoprotein (LDL) cholesterol(mg/dL), Triglyceride (TG) concentration(mg/dL)
Time Frame
week no. 0, 4, 12, 24
Title
Change in participant's Cortisol(ug/dL) level
Description
Metabolic indices
Time Frame
week no. 0, 4, 12, 24
Title
Change in participant's C-peptide(ng/dL)
Description
Metabolic indices
Time Frame
week no. 0, 4, 12, 24
Title
Change in participant's Inflammatory cytokines levels
Description
Metabolic indices; Fasting plasma C-reactive protein (CRP) level (pg/mL) + Oxytocin(pg/mL) + Leptin(mg/mL)
Time Frame
week no. 0, 4, 12, 24
Title
Change in participants's Quality of life scale (QOLs) scores [WHOQOL-BREF]
Description
Psychosocial variables as environment factors; Quality of Life Scale developed through the World Health Organization (WHOQOL-BREF) & Health-Related Quality of Life (HRQOL) questionnaires will be used as assessment tools WHOQOL-BREF: 4 domains will be assessed, consists of 1. Physical Health 2. Psychological 3. Social Relationship 4. Environment; [higher scores in each domains denote higher quality of life]
Time Frame
week no. 0, 4, 12, 24
Title
Change in participants's Quality of life scale (QOLs) scores [HRQOL]
Description
Psychosocial variables as environment factors; Quality of Life Scale developed through the World Health Organization (WHOQOL-BREF) & Health-Related Quality of Life (HRQOL) questionnaires will be used as assessment tools HRQOL: 4 domains will be assessed, consists of 1. Physical Health 2. Psychological 3. Level of independence 4. Social Relationship [higher scores in each domains denote higher quality of life]
Time Frame
week no. 0, 4, 12, 24
Title
Change in participant's Cognitive performance
Description
Continuous Performance Test (CPT)[visual information processing & attentive capacity], Finger Tapping Test (FPT), Wisconsin Card-Sorting Test (WCST)
Time Frame
week no. 0, 12, 24
Title
Change in participant's Social cognitive functional performance
Description
Mayer-Salovey-Caruso emotional Intelligence Test (MSCEIT) scores; perceiving + facilitating + understanding + managing emotion
Time Frame
week no. 0, 12, 24
Title
Change in participant's Microbiota profiles
Description
Fecal samples; Types of microorganisms + no. of colonies (colony-forming unit, CFU)
Time Frame
week no. 0, 12, 24

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Major depressive disorder (MDD) outpatients meet DSM- criteria Hamilton Rating Scale for Depression (HAM-D) ≥ 7 Start to receive fluoxetine or venlafaxine or those who have received the SSRI or SNRI antidepressants Exclusion Criteria: (A) had DSM-5 diagnosis for substance abuse within the past three months; (B) had taken monoamine oxidase inhibitors; (C) had an organic mental disorder, mental retardation, dementia, or other diagnosed neurological illness; (D) had a surgical condition or a major physical illness; (E) pregnant or breast-feeding.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Po-See Chen, Professor
Phone
866-6-2353535
Ext
5189
Email
chenps@mail.ncku.edu.tw
First Name & Middle Initial & Last Name or Official Title & Degree
Hui-Hua Chang, Professor
Phone
886-6-2353535
Ext
5683
Email
huihua@mail.ncku.edu.tw
Facility Information:
Facility Name
National Cheng-Kung University
City
Tainan
ZIP/Postal Code
704
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Po-See Chen, Professor
Phone
886-6-2353535
Ext
5189
Email
chenps@mail.ncku.edu.tw
First Name & Middle Initial & Last Name & Degree
Hui-Hua Chang, Professor
Phone
886-6-2353535
Ext
5683
Email
huihua@mail.ncku.edu.tw

12. IPD Sharing Statement

Plan to Share IPD
No
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Effects of Nutrients Supplementation in Antidepressant Treated Depressive Disorder Patients

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