RECRUITING

Patient Outcomes Collection: How Can we do Better?

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

Patient reported outcomes (PROs) are widely used by clinical providers as important tools to help inform their clinical and research practice, and to improve quality of care for patients. In this study, the investigators aim to investigate ways by which patient PRO completion rates may be improved.

Official Title

Patient Outcomes Collection: How Can we do Better? A Randomized Trial to Determine Factors Which May Affect Patient Compliance.

Quick Facts

Study Start:2019-04-30
Study Completion:2025-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03653455

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 to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients scheduled to undergo shoulder arthroscopy for rotator cuff condition (sub-acromial decompression, distal clavicle resection, biceps tenodesis, partial or full thickness rotator cuff tear repair or debridement) will be eligible for enrollment in the appropriate cohort. There will be no restrictions to this enrollment apart from that presented in the exclusions below.
  1. 1. Minors or those over the age of 80
  2. 2. Subjects lacking English proficiency to complete the PROs of interest.
  3. 3. Past or current medical history that would preclude patients from undergoing surgery.

Contacts and Locations

Study Contact

Carla M. Edwards, PhD
CONTACT
312-563-5735
carla_edwards@rush.edu
Nikhil Verma, MD
CONTACT
312-432-2819
verma.research@rushortho.com

Principal Investigator

Nikhil Verma, MD
PRINCIPAL_INVESTIGATOR
Rush University Medical Center

Study Locations (Sites)

Carla M. Edwards
Evanston, Illinois, 60201
United States

Collaborators and Investigators

Sponsor: Rush University Medical Center

  • Nikhil Verma, MD, PRINCIPAL_INVESTIGATOR, Rush University 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 Date2019-04-30
Study Completion Date2025-08-31

Study Record Updates

Study Start Date2019-04-30
Study Completion Date2025-08-31

Terms related to this study

Keywords Provided by Researchers

  • Shoulder
  • Arthroscopy
  • sub-acromial decompression
  • distal clavicle resection
  • biceps tenodesis
  • rotator cuff repair
  • Patient reported outcomes

Additional Relevant MeSH Terms

  • Shoulder Pain