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Microbiome and Axial Spondyloarthritis

Primary Purpose

Axial Spondyloarthritis

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Dietary recommendations
Sponsored by
Viome
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Axial Spondyloarthritis focused on measuring AxSpA, Microbiome, Viome, ASDAS, AS, Spondyloarthritis, HbA1c, Ankylosing, HLA B27, Spine, Ankylosing Spondylitis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • ICD-10 disease code or diagnosis for AxSpA
  • Confirmed diagnosis of AxSpA, based on ASDAS criteria including both non-radiographic axial spondyloarthritis and ankylosing spondylitis
  • HLA-B27 positive
  • Signed informed consent prior to any study-specific procedures are performed
  • Females and males aged 18 years or older
  • Able to read, speak and understand English
  • Willing and able to use the at-home collection kits and mail in pre-paid mailers
  • Willing and able to use a smartphone app or web app to answer surveys
  • Willing and able to make and keep/travel to a local lab visit for blood collection
  • Willing and able to follow the study instructions, as described in the recruitment letter

Exclusion Criteria:

  • Unable or unwilling to use Viome's App on an iPhone or Android smartphone
  • Not HLA-B27 positive
  • No diagnosis for AxSpA/AS
  • Pregnant or nursing
  • Other diagnosis of arthritis (rheumatoid, osteoarthritis, psoriatic arthritis, psoriatic spondyloarthritis)
  • IBD/Crohn's disease/ulcerative colitis
  • Use of antibiotics or Sulfasalazine within the past 3 months

Sites / Locations

  • Viome Research Institute online: https://www.viome.com/VRI/studies

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

All Study Participants

Arm Description

Enrolled with: AxSpA diagnosis, HLA-B27 positive, mASDAS > or = 1.3 and HLA-B27 positive. Will complete surveys online or on an app, about mental and physical health and how they are doing, submits and collection of samples (blood, stool, saliva, urine, fasting blood test at local lab). Receives results of some of the analysis of samples. Participants that qualify and complete the first set of samples can be eligible for the 3 and 6 month longitudinal follow-up collection kits. All participants receive dietary recommendations based on samples collected and the analysis of the microbiome.

Outcomes

Primary Outcome Measures

AxSpA (Axial Spondyloarthritis) disease activity
Analysis using lab results and AI learning models to correspond microbiome activity will be used to see if nutrition affects disease activity of the microbiome of people with AxSpA

Secondary Outcome Measures

Full Information

First Posted
August 31, 2020
Last Updated
July 5, 2022
Sponsor
Viome
Collaborators
Spondylitis Association of America (SAA)
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1. Study Identification

Unique Protocol Identification Number
NCT04713995
Brief Title
Microbiome and Axial Spondyloarthritis
Official Title
The Role of the Gut Microbiome in Axial Spondyloarthritis (AxSpA) Disease Activity
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Terminated
Why Stopped
Sufficient samples and data have been collected for data analyses.
Study Start Date
June 22, 2020 (Actual)
Primary Completion Date
June 15, 2022 (Actual)
Study Completion Date
June 15, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Viome
Collaborators
Spondylitis Association of America (SAA)

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
The purpose of this interventional study is to identify the root cause(s) of AxSpA (Axial Spondyloarthritis) relapses, which are likely due to the combination of nutrition, gut microbiome activities, leaky gut, and human genes (particularly from the immune system). This will be done by identifying molecular features of the microbiome that are associated with AxSpA flares, progression and relapses. The study will recruit participants with confirmed AxSpA diagnosis and who are HLA-B27 positive. During screening potential participants allow access to medical records to confirm eligibility requirements, such as diagnosis. Once enrolled, collection kits are sent to participants to collect samples using at-home collection kits and then provide a fasting blood sample at a local lab. Samples are then analyzed to identify features that likely cause AxSpA issues. Survey's are also answered to collect additional health data. Scientists will then use the data to identify the features that likely cause AxSpA flares and relapses.
Detailed Description
This is an Interventional study to help find the root causes of AxSpA relapses, flares and progression. The study will enroll 400 participants who are aged 18 or over, are HLA-B27 positive, have had a diagnosis of AxSpA. An informed consent form is acknowledged and medical release signed (to confirm eligibility criteria). Participants sign up online and answer questions about their physical and mental health and how they are doing (through an app and/or website). The participants will be in the study approximately 3 months, unless they agree to complete the 3 and 6 month timeline assessments for the longitudinal timelines, then the study will be completed after those timelines. If eligible, participants are shipped at-home collection kits which include: saliva, finger-prick blood and stool. A Genova urine test is also included to check intestinal permeability. Participants also make an appointment and go to a local lab to collect an additional blood sample. All samples are shipped via pre-paid mailers. All collections are done within a 1-week window (or 7 days). Clinical samples are collected in order to analyze specific molecular features associated with AxSpA in the microbiome found in participants. After shipping home collection kits and visiting the lab for a blood draw, participants receive diet recommendations which they will follow for ~3 months, after which time they will fill out a study survey to complete the first timeline in the study. If interested in participating in the longitudinal portion of the study, participants can also complete the 3-month and 6-month home collection, blood collection at the local lab and additional surveys. Scientists hope to find the microbiome and molecular information that corresponds to flares, health and wellness in the microbiome in patients with AxSpA.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Axial Spondyloarthritis
Keywords
AxSpA, Microbiome, Viome, ASDAS, AS, Spondyloarthritis, HbA1c, Ankylosing, HLA B27, Spine, Ankylosing Spondylitis

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
400 Participants are enrolled and paired matching for HLA-B27+ and control (mASDAS <1.3) and case group (mASDAS = or > 1.3) and compared to a healthy control group. Samples and surveys are collected from all participants. Then again at 3 months and 6 months if they agree to complete the longitudinal arms of the study.
Masking
None (Open Label)
Masking Description
All recruitment happens online. All nutritional recommendations look the same, but may be different between participants.
Allocation
N/A
Enrollment
95 (Actual)

8. Arms, Groups, and Interventions

Arm Title
All Study Participants
Arm Type
Other
Arm Description
Enrolled with: AxSpA diagnosis, HLA-B27 positive, mASDAS > or = 1.3 and HLA-B27 positive. Will complete surveys online or on an app, about mental and physical health and how they are doing, submits and collection of samples (blood, stool, saliva, urine, fasting blood test at local lab). Receives results of some of the analysis of samples. Participants that qualify and complete the first set of samples can be eligible for the 3 and 6 month longitudinal follow-up collection kits. All participants receive dietary recommendations based on samples collected and the analysis of the microbiome.
Intervention Type
Other
Intervention Name(s)
Dietary recommendations
Intervention Description
Dietary recommendations based on microbiome analysis of samples will be given and expected to receive and report in ~3 months survey after following recommendations.
Primary Outcome Measure Information:
Title
AxSpA (Axial Spondyloarthritis) disease activity
Description
Analysis using lab results and AI learning models to correspond microbiome activity will be used to see if nutrition affects disease activity of the microbiome of people with AxSpA
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: ICD-10 disease code or diagnosis for AxSpA Confirmed diagnosis of AxSpA, based on ASDAS criteria including both non-radiographic axial spondyloarthritis and ankylosing spondylitis HLA-B27 positive Signed informed consent prior to any study-specific procedures are performed Females and males aged 18 years or older Able to read, speak and understand English Willing and able to use the at-home collection kits and mail in pre-paid mailers Willing and able to use a smartphone app or web app to answer surveys Willing and able to make and keep/travel to a local lab visit for blood collection Willing and able to follow the study instructions, as described in the recruitment letter Exclusion Criteria: Unable or unwilling to use Viome's App on an iPhone or Android smartphone Not HLA-B27 positive No diagnosis for AxSpA/AS Pregnant or nursing Other diagnosis of arthritis (rheumatoid, osteoarthritis, psoriatic arthritis, psoriatic spondyloarthritis) IBD/Crohn's disease/ulcerative colitis Use of antibiotics or Sulfasalazine within the past 3 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Momochilo Vuyisich, PhD
Organizational Affiliation
Viome Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Viome Research Institute online: https://www.viome.com/VRI/studies
City
Bothell
State/Province
Washington
ZIP/Postal Code
98011
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Microbiome and Axial Spondyloarthritis

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