RECRUITING

Open Access Database of Standing Full Body Radiographs in Asymptomatic Volunteers

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

A study of the skeletal structure and how the structure changes over time. The aim of the study is to evaluate the skeleton in 10 year increments to determine an understanding of the normal skeleton as a person ages. By using x-ray analysis, a new low dose x-ray system (EOS) can be used to evaluate the whole body to see changes in the bone structure over time. Subjects will be asked to undertake one x-ray analysis of their whole body skeletal structure. There will be 25 male and 25 female subjects per decade. The averaging of the measured skeletal parameters will provide information on changes over time generating a standardized expectation of general changes in skeletal structure as participants age.

Official Title

Open Access Database of Standing Full Body Radiographs in Asymptomatic Volunteers

Quick Facts

Study Start:2016-09
Study Completion:2031-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT03076658

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:21 Years to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Males and females age 21-85 without a history of spine surgery.
  1. * History of spine or neural axis surgery
  2. * History of cancer with or without metastatic disease
  3. * Connective tissue, rheumatologic (or other inflammatory arthropathies), or neurologic disorders
  4. * History of knee replacement surgery, as these may have contractures causing unexpected changes in alignment
  5. * Severe osteoarthritis of the hips/knees/ankles
  6. * Spondylitis
  7. * Compression fractures or other trauma of the spinal column
  8. * Previous trauma/fractures of the pelvis whether or not surgery was required
  9. * Previous trauma or fractures of the lower extremities requiring surgery
  10. * Pregnant women
  11. * BMI \>37
  12. * Oswestry Disability Index score \>25

Contacts and Locations

Study Contact

David Calabrese
CONTACT
303-524-2550
david.calabrese@ucdenver.edu

Principal Investigator

Christopher Kleck, MD
PRINCIPAL_INVESTIGATOR
University of Colorado, Denver

Study Locations (Sites)

University of Coloardo Denver
Aurora, Colorado, 80045
United States

Collaborators and Investigators

Sponsor: University of Colorado, Denver

  • Christopher Kleck, MD, PRINCIPAL_INVESTIGATOR, University of Colorado, Denver

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 Date2016-09
Study Completion Date2031-01

Study Record Updates

Study Start Date2016-09
Study Completion Date2031-01

Terms related to this study

Additional Relevant MeSH Terms

  • Intervertebral Disc Degeneration
  • Osteoarthritis, Spine