CClinicalTrials.gg
CompletedNCT02524340Updated Sep 23, 2019

Patient Centered Adaptive Treatment Strategies Using Bayesian Causal Inference

An observational study in Juvenile Idiopathic Arthritis, sponsored by Children's Hospital Medical Center, Cincinnati. Completed at 1 site in United States. Open to participants aged 1 Year to 19 Years. Per ClinicalTrials.gov, last updated 2019-09-23.

Sponsored by Children's Hospital Medical Center, Cincinnati · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
465
Ages
1 Year to 19 Years
Sex
All
01

Study summary

The best treatment plan for Juvenile Idiopathic Arthritis (JIA) is often complicated. Patients and clinicians often don't know what is the best treatment strategy for a given patient at a given time. The purpose of this study is to develop a method to analyze data in situations where the treatment and disease state change over time. The researchers will develop a web-based package that will use the methods developed in this study. The package will be easy to use and allow dissemination of the methods to the public.

Read the detailed description

During routine clinical care, patients and physicians are often confronted with the following questions: "Given my (my child's) responses to the previous treatments, what is the best treatment option for me (my child)?" (by a patient/parent) and "What treatment should we recommend to patients who fail to respond to the first (or second) line of treatment?" (by a physician). Both questions are at the heart of patient centered outcomes research and clinical care, yet answers to these questions are seriously hindered by the lack of adequate analytic methods that appropriately take into account the fact that treatments, as well as the determinants of a treatment decision, vary over time during the course of the disease. Case in point: despite many medication options, polyarticular Juvenile Idiopathic Arthritis (pJIA) is often refractory, and requires better adaptive treatment strategies (ATS). Three ATS were recommended by a panel of experts for pJIA patients, but they need adequate analysis methods to evaluate and identify better ATS using observational data. Motivated by our patient-centered questions, and rigorously designed to evaluate the clinical effectiveness of patient centered adaptive treatment strategies (PCATS), the proposed method development will directly address: "development and dissemination of methods for adequate analysis of data in cases where the treatment/exposure varies over time", an area of interest identified by PCORI.

Accomplishing the proposed study will provide much needed double robust Bayesian causal inference methods that take the challenges of analyzing large registry and electronic health records including model uncertainty, large dimensional covariates and the unmeasured confounders, into account. A web-based userfriendly analytic computational package will be developed to allow easy application of the proposed methods. These developments will: 1) immediately offer methods and computational tools for evaluating clinical effectiveness and informing optimal ATS, 2) in the near future, enable shared-decision making tools for identifying optimal PCATS at the point-of-care, and 3) eventually enable a rapid learning system that will facilitate optimal PCATS. This study will have an immediate impact to children and stakeholders of JIA and a long-term broad impact to many chronically ill patients. Successful completion of this project will significantly move PCORI closer to its mission of helping "people make better informed healthcare decisions and improve healthcare delivery and outcomes".

02

Conditions studied

  • Juvenile Idiopathic Arthritis

Keywords

  • JIA
  • Arthritis
  • pcJIA
  • PCATS
03

In context

Arthritis

3,554 studies on the registry are indexed under Arthritis; 317 are open to participants now.

This study's enrollment of 465 is above the median of 155 across 1,057 observational studies indexed under Arthritis.

Browse Arthritis studies →

Lead sponsor

Children's Hospital Medical Center, Cincinnati is the lead sponsor of 661 studies on the registry; 134 are open to participants now.

Of its 54 completed or terminated interventional studies of FDA-regulated products, 30 (56%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Year to 19 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children less or equal to 19 years of age that have been diagnosed with ployarticular course of juvenile idiopathic arthritis.

Eligibility criteria

Participants should meet the following inclusion criteria:

  1. Age ≤19 years at baseline
  2. Diagnosed with ployarticular course of juvenile idiopathic arthritis (pcJIA) follow the operational case definition of pcJIA presented in Table 2 of the journal article published by Ringold et al. (2014).
  3. Meet new patient definition, i.e. diagnosed with pcJIA no more than 6 month at the first clinical encounter captured in the database
  4. Taken DMARDs no more than 9 months after diagnosed with pcJIA

Participants will be excluded if they meet the following exclusion criteria:

  1. Systematic JIA patients according to the ILAR code
  2. Patients with comorbidities of inflammatory bowel disease (IBD), celiac disease, and trisomy 21.
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
465 participants (actual)
Patient registry
No

Groups and cohorts

  • Juvenile Idiopathic Arthritis

    Children diagnosed with Juvenile Idiopathic Arthritis

06

What researchers measure

Primary outcomes

  1. Clinical response measured by clinical Juvenile Arthritis Disease Activity Score (cJADAS)

    Clinical trials outcome measurement based on 3 measures that are collected during office visits. The three measures are: active joint count, physician global assessment, and parent global evaluation.

    Time frame: 1 years

Secondary outcomes

  1. Quality of Life as measured by the Pediatric Quality of Life Inventory (PedsQL) survey

    PedsQL is a survey that measures the health-related quality of life in both healthy children and children with acute or chronic diseases.

    Time frame: 1 Years

07

Study locations

1 site
  • Cincinnati Children's Hospital Medical Center
    Cincinnati, Ohio 45229, United States
08

References and documents

Individual participant data

Plan to share: Yes — Data will be shared with PCORI.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 23, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02524340
Lead sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
Patient-Centered Outcomes Research Institute
Responsible party
Sponsor
First posted
Aug 14, 2015
Start date
Sep 2015
Primary completion
Jan 2019
Completion
Jan 2019
Last update
Sep 23, 2019

Study contacts

Bin Huang, PhD
principal investigator · Children's Hospital Medical Center, Cincinnati

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2018. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion