Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04441567

Right-Size Clinic Visits Using Memora Platform for PROMIS

Led by Boston Medical Center · Updated on 2025-10-14

3000

Participants Needed

1

Research Sites

277 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Developing novel methods of patient communication is crucial in providing value-based care to orthopedic patients. Healthcare technology platforms have been developed to improve patient communication methods particularly for the administration of patient-reported outcome measures (PROMs). However, the majority of these interventions rely on web-based platforms that require patients to have computer access. Among American households earning less than $30,000 per year, only 59% have access to a desktop or laptop and just 47% have broadband internet at home compared to mobile phone penetration which is estimated at 95% of which 93% regularly use text messages. The use of phone messaging may be the most effective means to have patients complete PROMs. The Patient-Reported Outcomes Measurement Information System (PROMIS) is an NIH-funded, clinically validated method of tracking patient-reported outcomes to efficiently assess patient health status. PROMIS utilizes Item Response Theory (IRT) and computerized adaptive testing (CAT) to improve measurement precision and decrease survey time as compared to traditional PROMs. The purpose of this two-phase study is to utilize Memora Health's text-messaging platform to collect web-based PROMIS CAT surveys from patients (Phase 1) and use this information to right-size clinic visits (Phase 2).

CONDITIONS

Official Title

Right-Size Clinic Visits Using Memora Platform for PROMIS

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with specific orthopedic conditions (ankle fracture, distal radius fracture, tibial plateau surgery, spine surgery or non-operative spine conditions, rotator cuff repair, or ACL reconstruction) within 3 weeks of enrollment or scheduled for surgery during enrollment
  • Personal use of a cellular phone with internet access
  • Primary language is English
Not Eligible

You will not qualify if you...

  • Limited or non-readers
  • Incarcerated patients or vulnerable populations
  • No access to a cell phone for completing surveys

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Boston Medical Center

Boston, Massachusetts, United States, 02118

Actively Recruiting

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Research Team

P

Paul Tornetta III, MD

CONTACT

K

Katarzyna Wegrzyn, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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