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Bone Health Management for Women Diagnosed With Breast Cancer

NCT02484131 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2017-03-27

No results posted yet for this study

Summary

The purpose of this study is to test the feasibility of the study protocol. The study protocol was designed to evaluate questions - "Do educational materials improve dual x-ray absorptiometry (DXA) screening rates for women diagnosed with breast cancer" and "Does educational materials delivered by the participant's selected choice change DXA screening rates compared to the conventional mail method?".

Conditions

Interventions

BEHAVIORAL

Educational materials/mail

Participants in this group will receive any educational materials by mail during hte follow-up period.

BEHAVIORAL

Educational materials/participant choice

Participants in this group will not receive any educational materials by participant choice during hte follow-up period.

Sponsors & Collaborators

  • British Columbia Cancer Agency

    collaborator OTHER

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Martin Dawes, MD, PhD · University of British Columbia

  • John J. Spinelli, PhD · British Columbia Cancer Agency

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
65 Years
Max Age
75 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2017-02-20
Completion
2017-03-20

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02484131 on ClinicalTrials.gov