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

Phase 2UnknownNCT05720793

Valerie Taylor20 enrolled

Overview

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.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Obsessive-Compulsive Disorder

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 Years

Medical Language ↔ Plain English

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

Outcomes

Primary Outcomes

Adverse Events

Reported Adverse events

Time frame: 0-13 weeks

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.

Time frame: 0-13 weeks

Secondary Outcomes

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.

Time frame: 0-13 weeks

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

Time frame: 0-13 weeks

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.

Time frame: 0-13 weeks

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.

Time frame: 0-13 weeks

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

Time frame: 0-13 weeks

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.

Time frame: 0-13 weeks

Next generation fecal, Urine, Blood and saliva sequencing

analysis of Fecal, urine, blood and saliva samples

Time frame: 0-13 weeks

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

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts