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Not yet recruitingNCT07865390Updated Oct 8, 2026

Patient-Reported Outcomes Dashboard With Goal Setting to Support Shared Decision-Making in Inflammatory Arthritis

An interventional study of Patient-Reported Outcomes Dashboard With Goal Setting in Arthritis, Psoriatic (PsA) and Arthritis, Rheumatoid (RA), sponsored by Northwestern University. Not yet recruiting at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-08.

Sponsored by Northwestern University · Not applicable, Interventional, and Health services research

Updated Oct 8, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
160
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The goal of this clinical trial is to learn whether showing patient-reported symptoms and personal treatment goals to rheumatology clinicians on a dashboard in the electronic health record improves shared decision-making for adults with rheumatoid arthritis or psoriatic arthritis.

The main questions it aims to answer are:

  • Do patients whose clinicians use the dashboard report more shared decision-making during their rheumatology visits than patients who receive usual care?
  • Do patients in the dashboard group report greater progress toward their personal goals and more confidence in managing their symptoms after 6 months?

Researchers will compare the dashboard group to a usual care group to see if the dashboard improves shared decision-making, goal attainment, and self-efficacy.

Participants will:

  • Complete a routine symptom questionnaire before their rheumatology visits, as all clinic patients do
  • Choose personal treatment goals and rate their progress toward those goals 6 months later
  • Complete short surveys before and after two rheumatology visits about 6 months apart

Participants in the dashboard group will also complete questionnaires in the patient portal about pain, fatigue, physical function, sleep, and morning stiffness before each visit. Their answers and goals will be shown to their clinician on a dashboard to guide the conversation during the visit.

02

Conditions studied

  • Arthritis, Psoriatic (PsA)
  • Arthritis, Rheumatoid (RA)

Keywords

  • Patient Reported Outcome Measures
  • Shared Decision Making
  • PROMIS
  • Goal Attainment Scaling
  • Electronic Health Records
  • Clinical Dashboard
  • Rheumatology
03

In context

Arthritis, Psoriatic

579 studies on the registry are indexed under Arthritis, Psoriatic; 132 are open to participants now.

This study's planned enrollment of 160 is above the median of 135 across 322 interventional studies indexed under Arthritis, Psoriatic.

Browse Arthritis, Psoriatic studies →

Lead sponsor

Northwestern University is the lead sponsor of 1,398 studies on the registry; 201 are open to participants now.

Of its 102 completed or terminated interventional studies of FDA-regulated products, 73 (72%) have results posted.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age 18 years or older
  • Diagnosis of rheumatoid arthritis or psoriatic arthritis
  • Receiving care at a Northwestern Medicine rheumatology clinic, with an upcoming rheumatology visit
  • Active patient portal (MyChart) account
  • Able to read and complete questionnaires in English
  • Able to provide informed consent

Exclusion criteria

Exclusion Criteria:

  • Unable to provide informed consent
  • Unable to complete study questionnaires in English
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
160 participants (estimated)

Study arms

  • Experimental
    PRO Dashboard With Goal Setting

    Before each of two routine rheumatology visits approximately 6 months apart, participants complete the RAPID3 (standard of care for all clinic patients) plus an additional questionnaire series in the patient portal: selection of personal treatment goals, a morning stiffness question, and four PROMIS computer adaptive tests (Pain Interference, Fatigue, Physical Function, and Sleep Disturbance). Responses and goals are displayed to the treating clinician on a dashboard in the electronic health record for use during the visit.

    Other: Patient-Reported Outcomes Dashboard With Goal Setting

  • No intervention
    Usual Care

    Participants receive usual rheumatology care. They do not receive the additional questionnaire series, and no study dashboard is displayed to the clinician. For outcome assessment only, participants select personal goals and rate goal attainment in study surveys that are not shared with the clinician.

Interventions

  • OtherPatient-Reported Outcomes Dashboard With Goal Setting

    A clinician-facing dashboard embedded in the Epic electronic health record that displays the participant's PROMIS computer adaptive test (CAT) scores (PROMIS Pain Interference, PROMIS Fatigue, PROMIS Physical Function, PROMIS Sleep Disturbance), morning stiffness, and self-selected treatment goals collected through the patient portal before the visit. Clinicians receive training on using the dashboard to support shared decision-making and goal-directed care during the visit.

06

What researchers measure

Primary outcomes

  1. Shared Decision-Making

    CollaboRATE is a 3-item patient-reported measure of shared decision-making during a clinical encounter. Each item is rated from 0 (no effort was made) to 9 (every effort was made). The score is the mean of the three items (range 0 to 9); higher scores indicate more shared decision-making.

    Time frame: Within 48 hours after the second study visit (approximately 6 months after enrollment)

07

Study locations

1 site
  • Northwestern Medicine Rheumatology
    Chicago, Illinois 60611, United States
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 8, 2026
Show all 1 update
  1. Oct 8, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07865390
Lead sponsor
Northwestern University
Responsible party
Maja Kuharic (Assistant Professor, Northwestern University) — Principal investigator
First posted
Oct 8, 2026
Start date
Nov 16, 2026 (estimated)
Primary completion
Dec 31, 2027 (estimated)
Completion
Feb 29, 2028 (estimated)
Last update
Oct 8, 2026

Study contacts

MAJA KUHARIC, Msc, PhD
Contact
maja.kuharic@northwestern.edu
9045547009

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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