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A Clinical Trial of Fecal Microbiota Transplantation in a Population With Obsessive-compulsive Disorder (FOCUSED)

Primary Purpose

Obsessive-Compulsive Disorder

Status
Not yet recruiting
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
FMT Capsule + SIMBA Capsule
Sponsored by
Valerie Taylor
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obsessive-Compulsive Disorder focused on measuring OCD, Microbiome, FMT, Gut bacteria

Eligibility Criteria

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

Inclusion Criteria: Adults who have a primary diagnosis of OCD on a stable appropriate dose of (SSRI) treatment for at least 12 weeks prior to Baseline insufficient response to current SSRI treatment indicated by persistence of symptoms. Exclusion Criteria: Participant meets Diagnostic criteria for substance use, eating disorder, schizophrenia, or schizoaffective disorder Suicidality regular intake of antibiotics, prebiotics, or probiotics Clinically diagnosed with IBD, Crohn's disease, Ulcerative colitis, or Celiac disease Immune suppression intestinal obstruction Oropharyngeal dysphagia or other swallowing disorder < 2 bowel movements per week Breastfeeding, pregnant or seeking to get pregnant during the course of this study

Sites / Locations

  • University of Calgary, TRW building

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

FMT capsule + SIMBA Capsule

Arm Description

adults with OCD who are being treated with an approved first line treatment for OCD medication will be assigned to receive FMT capsules as an adjunct treatment.

Outcomes

Primary Outcome Measures

Adverse Events
Reported Adverse events
Toronto Side Effects Scale (TSES)
Changes in the Toronto Side Effects Scale (TSES). TSES a 32-item instrument used to evaluate the incidence, frequency, and severity of the central nervous system (CNS), gastrointestinal (GI), and sexual side effects.

Secondary Outcome Measures

Global function/overall improvement (Quick Inventory of Depressive Symptomatology-Self-Report (QIDS))
Quick Inventory of Depressive Symptomatology-Self-Report (QIDS). is a 16-item questionnaire that rates depression symptoms via self-assessment. Toral score is calculated but summing the scores of each of the 16 different questions. 0-5 Normal, 6-10 mild depression, 11-15 Moderate depression, 16-20 Severe depression and >21 is considered very severe depression.
Global function/overall improvement (The General Anxiety Disorder-7 scale (GAD-7))
The General Anxiety Disorder-7 scale (GAD-7). The 7-item tool is used to screen and assess for generalized anxiety. Score 0-4: Minimal Anxiety, Score 5-9: Mild Anxiety, Score 10-14: Moderate Anxiety and Score greater than 15: Severe Anxiety
Global function/overall improvement (Positive and Negative Affect Schedule (PANAS))
Positive and Negative Affect Schedule (PANAS). The PANAS is a self-report questionnaire that consists of two 10-item scales and measures both positive and negative emotions for participants. The total score is calculated by finding the sum of the 10 positive items, and then the 10 negative items. Scores range from 10 - 50 for both sets of items. higher score indicates more positive or negative affect respectively.
Global function/overall improvement (Patient Health Questionnaire-9(PHQ9))
Patient Health Questionnaire-9(PHQ9). The PHQ9 is used for screening and measuring the severity of depressive symptoms. The total score is the sum the numbers of all the checked responses under each heading. Cut off scores are: 0 - 4 None, 5 - 9 Mild, 10 - 14 Moderate, 15 - 19 Moderately Severe and 20 - 27 Severe.
OCD symptoms (Y-BOCS)
Yale-Brown Obsessive Compulsive Scale (Y-BOCS). Total scores range from 0 to 40. 0-7 indicates subclinical symptoms, 8-15 mild symptoms, 16-23 moderate symptoms, 24-31 severe symptoms and 32-40 extreme symptoms
OCD symptoms (TOCS)
Toronto Obsessive-Compulsive Scale (TOCS). TOCS is a 21 item self-reported questionnaire that assesses several major symptom dimensions in OCD. A total score is calculated by adding each score of the 21 items, and dimension scores are calculated by averaging the sum of item scores within each dimension.
Next generation fecal, Urine, Blood and saliva sequencing
analysis of Fecal, urine, blood and saliva samples

Full Information

First Posted
January 26, 2023
Last Updated
February 7, 2023
Sponsor
Valerie Taylor
Collaborators
Nimble Science Ltd., University of Calgary
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1. Study Identification

Unique Protocol Identification Number
NCT05720793
Brief Title
A Clinical Trial of Fecal Microbiota Transplantation in a Population With Obsessive-compulsive Disorder
Acronym
FOCUSED
Official Title
A Clinical Trial to Evaluate the Safety and Tolerability of Fecal Microbiota Transplantation in a Population With Obsessive-compulsive Disorder
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 1, 2023 (Anticipated)
Primary Completion Date
March 1, 2024 (Anticipated)
Study Completion Date
August 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Valerie Taylor
Collaborators
Nimble Science Ltd., University of Calgary

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
Obsessive-compulsive disorder (OCD) is a psychiatric condition marked by recurrent intrusive thoughts (obsessions) and ritualistic behaviors aimed at reducing distress (compulsions). While there exist a number of medications to treat this illness, half of those who need them either do not respond or can not tolerate current medications because of side effects. Therefore, there is an urgent need to develop new ways to treat this illness. One of the areas being explored as a potential option is based on what is now known as a strong link between the bacteria that live in our gut and the brain. Research has shown that a fecal transplant of the gut bacteria from healthy donors is able to improve health outcomes for people with depression and the investigators now want to expand this into OCD, given a known link between this condition and bacterial infection. To do this the investigators will use both the standard methods of bacterial identification via stool analysis, which looks at large bowel changes, and compare it to the Small Intestine Microbiome Aspiration (SIMBA) system, a small capsule that when swallowed allows a fluid sample to be collected from the participants' small intestine. This work will help the investigators assess the benefits of fecal transplant in OCD, and more importantly, identify how transplant changes the system, utilizing a novel technology to move the field forward.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obsessive-Compulsive Disorder
Keywords
OCD, Microbiome, FMT, Gut bacteria

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
FMT capsule + SIMBA Capsule
Arm Type
Experimental
Arm Description
adults with OCD who are being treated with an approved first line treatment for OCD medication will be assigned to receive FMT capsules as an adjunct treatment.
Intervention Type
Combination Product
Intervention Name(s)
FMT Capsule + SIMBA Capsule
Intervention Description
Participants in this arm will receive FMT capsules in addition to their usual treatment. participants will also be administered SIMBA sample collection capsules.
Primary Outcome Measure Information:
Title
Adverse Events
Description
Reported Adverse events
Time Frame
0-13 weeks
Title
Toronto Side Effects Scale (TSES)
Description
Changes in the Toronto Side Effects Scale (TSES). TSES a 32-item instrument used to evaluate the incidence, frequency, and severity of the central nervous system (CNS), gastrointestinal (GI), and sexual side effects.
Time Frame
0-13 weeks
Secondary Outcome Measure Information:
Title
Global function/overall improvement (Quick Inventory of Depressive Symptomatology-Self-Report (QIDS))
Description
Quick Inventory of Depressive Symptomatology-Self-Report (QIDS). is a 16-item questionnaire that rates depression symptoms via self-assessment. Toral score is calculated but summing the scores of each of the 16 different questions. 0-5 Normal, 6-10 mild depression, 11-15 Moderate depression, 16-20 Severe depression and >21 is considered very severe depression.
Time Frame
0-13 weeks
Title
Global function/overall improvement (The General Anxiety Disorder-7 scale (GAD-7))
Description
The General Anxiety Disorder-7 scale (GAD-7). The 7-item tool is used to screen and assess for generalized anxiety. Score 0-4: Minimal Anxiety, Score 5-9: Mild Anxiety, Score 10-14: Moderate Anxiety and Score greater than 15: Severe Anxiety
Time Frame
0-13 weeks
Title
Global function/overall improvement (Positive and Negative Affect Schedule (PANAS))
Description
Positive and Negative Affect Schedule (PANAS). The PANAS is a self-report questionnaire that consists of two 10-item scales and measures both positive and negative emotions for participants. The total score is calculated by finding the sum of the 10 positive items, and then the 10 negative items. Scores range from 10 - 50 for both sets of items. higher score indicates more positive or negative affect respectively.
Time Frame
0-13 weeks
Title
Global function/overall improvement (Patient Health Questionnaire-9(PHQ9))
Description
Patient Health Questionnaire-9(PHQ9). The PHQ9 is used for screening and measuring the severity of depressive symptoms. The total score is the sum the numbers of all the checked responses under each heading. Cut off scores are: 0 - 4 None, 5 - 9 Mild, 10 - 14 Moderate, 15 - 19 Moderately Severe and 20 - 27 Severe.
Time Frame
0-13 weeks
Title
OCD symptoms (Y-BOCS)
Description
Yale-Brown Obsessive Compulsive Scale (Y-BOCS). Total scores range from 0 to 40. 0-7 indicates subclinical symptoms, 8-15 mild symptoms, 16-23 moderate symptoms, 24-31 severe symptoms and 32-40 extreme symptoms
Time Frame
0-13 weeks
Title
OCD symptoms (TOCS)
Description
Toronto Obsessive-Compulsive Scale (TOCS). TOCS is a 21 item self-reported questionnaire that assesses several major symptom dimensions in OCD. A total score is calculated by adding each score of the 21 items, and dimension scores are calculated by averaging the sum of item scores within each dimension.
Time Frame
0-13 weeks
Title
Next generation fecal, Urine, Blood and saliva sequencing
Description
analysis of Fecal, urine, blood and saliva samples
Time Frame
0-13 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: Adults who have a primary diagnosis of OCD on a stable appropriate dose of (SSRI) treatment for at least 12 weeks prior to Baseline insufficient response to current SSRI treatment indicated by persistence of symptoms. Exclusion Criteria: Participant meets Diagnostic criteria for substance use, eating disorder, schizophrenia, or schizoaffective disorder Suicidality regular intake of antibiotics, prebiotics, or probiotics Clinically diagnosed with IBD, Crohn's disease, Ulcerative colitis, or Celiac disease Immune suppression intestinal obstruction Oropharyngeal dysphagia or other swallowing disorder < 2 bowel movements per week Breastfeeding, pregnant or seeking to get pregnant during the course of this study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Asem Bala, Msc, CCRP
Phone
4032107282
Email
asem.bala@ucalgary.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Vivek Kumar, MD
Phone
403-210-8650
Email
vivek.kumar@ucalgary.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Valere Taylor, MD,PhD,FRCPC
Organizational Affiliation
Professor, Head of Department
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary, TRW building
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 4Z6
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
We will also share our results via the "Gut Microbiota for Health Experts exchange", an online community where experts in this field share news, innovation and information on topics pertaining to the gut microbiota (www.gutmicrobiotaforhealth.com). This organization has over 10 000 online members and a large social media presence. Manuscripts will be published in scientific journals
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A Clinical Trial of Fecal Microbiota Transplantation in a Population With Obsessive-compulsive Disorder

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