RECRUITING

Right-Size Clinic Visits Using Memora Platform for PROMIS

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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).

Official Title

Patient Reported Outcomes Measures Pilot Grant for Orthopedic Patients

Quick Facts

Study Start:2021-05-10
Study Completion:2025-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04441567

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Subjects that are classified by the Current Procedural Terminology/International Classification of Diseases (CPT/ICD)-10 Diagnosis Codes, having sustained the injury within 3 weeks of enrollment for non-operative treatment or will undergo surgery during the enrollment period:
  2. * Ankle Fracture
  3. * Distal Radius Fracture
  4. * Tibial Plateau Open reduction internal fixation (ORIF)
  5. * Spine Operative
  6. * Anterior cervical discectomy with fusion (ACDF)
  7. * Cervical Laminectomy
  8. * Lumbar Fusion
  9. * Lumbar Decompression
  10. * Spine Non-operative
  11. * Lumbar Stenosis
  12. * Lumbar Degenerative Disc Disease
  13. * Rotator Cuff Repair
  14. * Anterior cruciate ligament (ACL) Reconstruction
  15. * Have personal use of cellular phone with access to the internet
  16. * Speak either English or English as a primary language:
  1. * Limited and non-readers
  2. * Vulnerable populations - incarcerated patients
  3. * Patients with no cell phone to use for scoring

Contacts and Locations

Study Contact

Paul Tornetta III, MD
CONTACT
617 414 5757
Paul.Tornetta@bmc.org
Katarzyna Wegrzyn, MD
CONTACT
617-414-5757
Katarzyna.Wegrzyn@bmc.org

Principal Investigator

Paul Tornetta III, MD
PRINCIPAL_INVESTIGATOR
Boston Medical Center

Study Locations (Sites)

Boston Medical Center
Boston, Massachusetts, 02118
United States

Collaborators and Investigators

Sponsor: Boston Medical Center

  • Paul Tornetta III, MD, PRINCIPAL_INVESTIGATOR, Boston Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-05-10
Study Completion Date2025-06

Study Record Updates

Study Start Date2021-05-10
Study Completion Date2025-06

Terms related to this study

Keywords Provided by Researchers

  • PROM
  • PROMIS
  • Memora Health Text messaging platform
  • SMS (Short Message Service)
  • Orthopedic conditions
  • Recovery curves
  • Right-size clinic visits
  • CAT
  • SMS

Additional Relevant MeSH Terms

  • Orthopedic Disorders