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A 12-weeks Study to Evaluate the Dietary Fiber and Probiotics Treatment in Prevention and Intervention of Weight-gain and Cognitive Impairment of Schizophrenia or Bipolar Disorder

Primary Purpose

Schizophrenia, Bipolar Disorder

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Bifico (Live combined bifidobacterium,Lactobacillus and Enterococcus capsules, Oral)
Dietary fiber
Sponsored by
Central South University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring Schizophrenia, probiotics, cognitive impairment, Metabolic syndrome, clinical trail, Efficacy, Safety, Dietary fiber, Bipolar Disorder

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Meet the Diagnostic and Statistical Manual (DSM-V) diagnostic criteria for schizophrenia or bipolar disorder;
  2. Patients with a weight gain of more than 10% after taking antipsychotic medications;
  3. Male and female with aged 18 to 65 years;
  4. PANSS total score < 60 or HAMD-17 total score≤ 7 and YMRS total score<5;
  5. Signed the study consent for participation;
  6. Not allergy to probiotics or dietary fiber medicine
  7. On stable medication and dosage for at least 3 months.

Exclusion Criteria:

  1. Having history of substance dependence or abuse or whose symptoms are caused by the other diagnosable mental disorders;
  2. Having history of traumatic brain injury, seizures or other known neurological or organic diseases of the central nervous system;
  3. Taking antidepressants, stimulants, mood stabilizer or accepts electricity shock treatment;
  4. Having current suicidal or homicidal thoughts or any safety concern by research staff that cannot be manage in an inpatient setting;
  5. The routine blood tests showing abnormal renal, liver function;
  6. Pregnant or lactating women.
  7. No administration of any antibiotics in two mouths

Sites / Locations

  • The Second Xiangya Hospital of Central South University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

No Intervention

Experimental

Experimental

Arm Label

Probiotics Group

Control Group

Dietary fiber Group

Dietary fiber Probiotics group

Arm Description

Probiotics add-on treatment :(live Combined Bifidobacterium, Lactobacillus and Enterococcus Capsules, Oral), each capsule contain more then 1.0*10^7 CFU. Bifico: 840mg Bid.

No probiotics or dietary fiber group.

Prebiotics add-on treatment: dietary fibers compound powder, 30g bid

Dietary fiber and probiotics group: receiving both Bifico 840mg Bid and dietary fiber 30g bid.

Outcomes

Primary Outcome Measures

MATRICS Consensus Cognitive Battery (MCCB) composite score
The investigators will use the MATRICS Consensus Cognitive Battery (MCCB) Composite score as primary cognitive outcome measure before and after treatment at different follow up point.
Body Mass Index
The body mass index (BMI) or Quetelet index is a value derived from the mass (weight) and height of an individual. The BMI is defined as the body mass divided by the square of the body height, and is universally expressed in units of kg/m2, resulting from mass in kilograms and height in metres.

Secondary Outcome Measures

Positive And Negative Syndrome Scale (PANSS)
The change of Positive And Negative Syndrome Scale (PANSS) total, positive and negative symptoms before and after treatment at different follow up point.
Lipid metabolism related blood index
Other lipid metabolism related marker such as LDL,HDL,TG, CHO (all in mmol/L)
Physical exam index
Body weight related physical exam index: waist circumference,hip line (cm)
Hamilton Depression Scale and Young Manic Rating Scale (YMRS)
The change of total score of the Hamilton Depression Scale and the Young Manic Rating Scale (YMRS), used to measure mania and depression symptoms of bipolar disorder.

Full Information

First Posted
November 29, 2017
Last Updated
April 18, 2023
Sponsor
Central South University
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1. Study Identification

Unique Protocol Identification Number
NCT03379597
Brief Title
A 12-weeks Study to Evaluate the Dietary Fiber and Probiotics Treatment in Prevention and Intervention of Weight-gain and Cognitive Impairment of Schizophrenia or Bipolar Disorder
Official Title
A 12-weeks Study to Evaluate the Dietary Fiber and Probiotics Treatment in Prevention and Intervention of Weight-gain and Cognitive Impairment of Schizophrenia or Bipolar Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
November 30, 2017 (Actual)
Primary Completion Date
May 31, 2021 (Actual)
Study Completion Date
June 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Central South University

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
In this study, the investigators will evaluate the efficacy, safety and related mechanism of dietary fiber and probiotics alone and in combination as a add-on treatment in improving the antipsychotic induced weight gain, the cognitive impairment, and psychotic syndrome in schizophrenia or bipolar disorder patients. The study will recruit 100 schizophrenia or bipolar disorder patients who meet the criteria of DSM-5, and then randomized to 4 groups: probiotics group(PB group) dietary fiber group(FB group) probiotics plus dietary fiber group(PF group) and control group(CT group) for a 12-weeks clinical trail. The specific aims are to compare probiotics group versus controls on: 1) clinical core symptoms; 2) cognition;3)metabolic related markers.
Detailed Description
In this study, the investigators will evaluate the efficacy, safety and related mechanism of dietary fiber and probiotics alone and in combination as a add-on treatment in improving the antipsychotic induced weight gain, the cognitive impairment, and psychotic syndrome in schizophrenia or bipolar disorder patients. The study will recruit 100 schizophrenia or bipolar disorder patients who meet the criteria of DSM-5, and then randomized to 4 groups: probiotics group(PB group) dietary fiber group(FB group) probiotics plus dietary fiber group(PF group) and control group(CT group) for a 12-weeks clinical trail (20 patients per arm) for a 12-weeks clinical trail. Clinical efficacy and safety assessment will be done at screen/baseline, 4 week, 8 week and 12 week. The specific aims are to compare probiotics group versus controls on: 1) clinical core symptoms; 2) cognition; 3) metabolic related markers. Biological samples also will be collected, and stored to research related mechanisms. Clinical symptoms will be measured by the Positive and Negative Syndrome Scale,. Cognitive function will be assessed by the MATRICS Consensus Cognitive Battery. The investigators hypothesize that: 1) dietary fiber and probiotics may improve cognitive impairment of patients with schizophrenia; 2) dietary fiber and probiotics could prevent the cognitive decline of patients with schizophrenia; 3)dietary fiber and probiotics may prevent the antipsychotics induced weight gain in patients with schizophrenia.4)dietary fiber and probiotics may alter oxidative stress indexes or inflammatory biomarkers thus influence the oxidative and inflammatory mechanism.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia, Bipolar Disorder
Keywords
Schizophrenia, probiotics, cognitive impairment, Metabolic syndrome, clinical trail, Efficacy, Safety, Dietary fiber, Bipolar Disorder

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Probiotics Group
Arm Type
Experimental
Arm Description
Probiotics add-on treatment :(live Combined Bifidobacterium, Lactobacillus and Enterococcus Capsules, Oral), each capsule contain more then 1.0*10^7 CFU. Bifico: 840mg Bid.
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
No probiotics or dietary fiber group.
Arm Title
Dietary fiber Group
Arm Type
Experimental
Arm Description
Prebiotics add-on treatment: dietary fibers compound powder, 30g bid
Arm Title
Dietary fiber Probiotics group
Arm Type
Experimental
Arm Description
Dietary fiber and probiotics group: receiving both Bifico 840mg Bid and dietary fiber 30g bid.
Intervention Type
Drug
Intervention Name(s)
Bifico (Live combined bifidobacterium,Lactobacillus and Enterococcus capsules, Oral)
Intervention Description
Bifico 840mg Bid
Intervention Type
Dietary Supplement
Intervention Name(s)
Dietary fiber
Intervention Description
dietary fiber compound powder 30g bid
Primary Outcome Measure Information:
Title
MATRICS Consensus Cognitive Battery (MCCB) composite score
Description
The investigators will use the MATRICS Consensus Cognitive Battery (MCCB) Composite score as primary cognitive outcome measure before and after treatment at different follow up point.
Time Frame
12 weeks
Title
Body Mass Index
Description
The body mass index (BMI) or Quetelet index is a value derived from the mass (weight) and height of an individual. The BMI is defined as the body mass divided by the square of the body height, and is universally expressed in units of kg/m2, resulting from mass in kilograms and height in metres.
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Positive And Negative Syndrome Scale (PANSS)
Description
The change of Positive And Negative Syndrome Scale (PANSS) total, positive and negative symptoms before and after treatment at different follow up point.
Time Frame
12 weeks
Title
Lipid metabolism related blood index
Description
Other lipid metabolism related marker such as LDL,HDL,TG, CHO (all in mmol/L)
Time Frame
12 weeks
Title
Physical exam index
Description
Body weight related physical exam index: waist circumference,hip line (cm)
Time Frame
12 weeks
Title
Hamilton Depression Scale and Young Manic Rating Scale (YMRS)
Description
The change of total score of the Hamilton Depression Scale and the Young Manic Rating Scale (YMRS), used to measure mania and depression symptoms of bipolar disorder.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meet the Diagnostic and Statistical Manual (DSM-V) diagnostic criteria for schizophrenia or bipolar disorder; Patients with a weight gain of more than 10% after taking antipsychotic medications; Male and female with aged 18 to 65 years; PANSS total score < 60 or HAMD-17 total score≤ 7 and YMRS total score<5; Signed the study consent for participation; Not allergy to probiotics or dietary fiber medicine On stable medication and dosage for at least 3 months. Exclusion Criteria: Having history of substance dependence or abuse or whose symptoms are caused by the other diagnosable mental disorders; Having history of traumatic brain injury, seizures or other known neurological or organic diseases of the central nervous system; Taking antidepressants, stimulants, mood stabilizer or accepts electricity shock treatment; Having current suicidal or homicidal thoughts or any safety concern by research staff that cannot be manage in an inpatient setting; The routine blood tests showing abnormal renal, liver function; Pregnant or lactating women. No administration of any antibiotics in two mouths
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
DongYu Kang, M.D.
Organizational Affiliation
Central South University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
SuJuan Li, M.D.
Organizational Affiliation
Central South University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
RenRong Wu, M.D. Ph.D.
Organizational Affiliation
Central South University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Chenchen Liu, M.D.
Organizational Affiliation
Central South University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Second Xiangya Hospital of Central South University
City
Changsha
State/Province
Hunan
ZIP/Postal Code
410011
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
33622382
Citation
Liu C, Kang D, Xiao J, Huang Y, Peng X, Wang W, Xie P, Yang Y, Zhao J, Wu R. Dietary fiber and probiotics for the treatment of atypical antipsychotic-induced metabolic side effects: study protocol for a randomized, double-blind, placebo-controlled trial. Trials. 2021 Feb 23;22(1):159. doi: 10.1186/s13063-021-05123-w.
Results Reference
derived

Learn more about this trial

A 12-weeks Study to Evaluate the Dietary Fiber and Probiotics Treatment in Prevention and Intervention of Weight-gain and Cognitive Impairment of Schizophrenia or Bipolar Disorder

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