C-STOP Fracture Trial (C-STOP#)
Primary Purpose
Osteoporosis
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
case management
Multifaceted quality improvement intervention
Sponsored by
About this trial
This is an interventional health services research trial for Osteoporosis focused on measuring osteoporosis, fracture, treatment, guidelines, quality
Eligibility Criteria
Inclusion Criteria:
- age 50 years or greater
- any forearm (distal radius or ulna, "wrist") or arm (proximal humerus, "upper arm") fracture
Exclusion Criteria:
- unable to give simple informed consent or unwilling to participate in the study
- unable to understand, read, and converse in English
- presence of pathological (e.g., cancer related) or multiple (e.g., major trauma) fractures
- already treated for osteoporosis with a bisphosphonate
- residence in a nursing home or from outside Edmonton
Sites / Locations
- University of Alberta Hospitals
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Case Manager Intervention
Multifaceted quality improvement intervention
Arm Description
Osteoporosis case-managers will identify older fracture patients in Emergency Departments and Fracture Clinics; arrange bone mineral density (BMD) tests; meet with patients to counsel them and go over their results; and then offer and prescribe bisphosphonate treatment to those with low BMD.
Active-comparator control consisting of telephone-based education for patients and treatment guidelines with reminders for family physicians
Outcomes
Primary Outcome Measures
Proportion of untreated patients newly starting prescription osteoporosis treatment with a bisphosphonate after their fracture
Proportion of previously untreated patients (%) newly starting prescription osteoporosis treatment with a bisphosphonate within 6-months of an upper extremity fragility fracture
Secondary Outcome Measures
New Treatment Persistence
Of those newly starting treatment, what proportion are still persisting with it at 1-year of followup
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01401556
Brief Title
C-STOP Fracture Trial
Acronym
C-STOP#
Official Title
Comparing Strategies Targeting Osteoporosis to Prevent Recurrent Fractures: C-STOP# Randomized Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2020
Overall Recruitment Status
Completed
Study Start Date
September 2012 (Actual)
Primary Completion Date
December 2019 (Actual)
Study Completion Date
April 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Alberta
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The objective of the proposed research is to improve quality of care for older outpatients who present to Emergency Departments and Fracture Clinics with an osteoporosis-related wrist or other upper extremity fracture. Although most of these patients warrant evidence-based and guideline-recommended osteoporosis testing and treatment, numerous studies demonstrate treatment rates less than 10-20% in the year post-fracture. Several trials, including the investigators own prior studies, have tried to address this osteoporosis care-gap and have reported that various multifaceted interventions (combinations of patient and physician education, guidelines, and physician reminders) can modestly improve treatment rates compared with usual care, although 60-70% of the patients exposed to these interventions still remain untreated. The investigators believe that a case-manager (who identifies and independently sees patients in clinic, arranges bone mineral density [BMD] tests, and offers guideline-based treatment to those with low BMD) represents a potential solution that holds great promise.
The investigators hypothesize that an osteoporosis case-manager will effectively and efficiently increase rates of osteoporosis treatment in older outpatients with upper extremity fractures when compared with a documented effective and cost-saving multifaceted intervention. To test this hypothesis the investigators propose a pragmatic patient-level randomized controlled comparative effectiveness trial with blinded outcomes ascertainment that compares the case-manager strategy with the multifaceted intervention.
Detailed Description
Objective: To improve treatment of osteoporosis in older patients with upper extremity fractures.
Background: Osteoporosis causes low bone mass and skeletal fragility leading to fractures of the hip, spine, and upper extremity that cause pain, deformity, disability, and even death. It affects 2 million older Canadians and costs us a billion dollars a year. Guidelines recommend aggressive treatment in older patients with osteoporosis-related fractures because risk of another fracture is 20% within 1-year and because bisphosphonate treatment reduces fracture risk by 50%. Unfortunately, less than 10% of older outpatients are treated for osteoporosis in the year post-fracture and even the most effective multifaceted interventions tested so far (i.e., combinations of patient education with physician guidelines and reminders) have only increased post-fracture osteoporosis treatment rates with bisphosphonates to 22%.
Proposed Strategy: Osteoporosis case-managers will identify older fracture patients in Emergency Departments and Fracture Clinics; arrange bone mineral density (BMD) tests; meet with patients to counsel them and go over their results; and then offer and prescribe bisphosphonate treatment to those with low BMD.
Hypothesis: An osteoporosis case-manager will effectively and efficiently increase rates of BMD testing and bisphosphonate treatment in older high-risk patients with upper extremity fractures compared with a previously tested effective and cost-saving multifaceted osteoporosis intervention (an active-comparator control consisting of telephone-based education for patients and treatment guidelines with reminders for family physicians).
Specific Aims: To determine whether an osteoporosis case-manager strategy can:
Increase rates of osteoporosis treatment more than a multifaceted intervention
Increase rates of BMD testing more than a multifaceted intervention
Be cost-effective when compared with either multifaceted intervention or usual care
Study Design: Randomized controlled comparative effectiveness trial with blinded (allocation-concealed) ascertainment of outcomes comparing case-managers to the multifaceted intervention. Eligible patients will be 50 years and older with an upper extremity fracture and not already treated with bisphosphonates, recruited from Emergency Departments and Fracture Clinics. Primary outcome will be the proportion starting bisphosphonates within 6-months. Secondary outcomes include BMD testing, any osteoporosis treatment, and appropriate care. Case-managers are expected to increase bisphosphonate treatment rates to 43% (achieved in our pilot trial) vs published multifaceted intervention rates of 22%. With alpha=0.05, beta=0.9, and 10% attrition rates, the total minimum required sample size is 240 patients. Using 1-year outcomes and micro-costing data from the trial and our published Markov decision analytic model for osteoporosis quality improvement interventions, the incremental costs and effectiveness of the case-manager will then be compared to both the multifaceted intervention and usual care. Major secondary outcome includes long-term treatment persistence, and to examine this question (e.g., 80% persistence rates with case-manager vs 50% persistence with multifaceted intervention) will require a sample size of at least 360 patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoporosis
Keywords
osteoporosis, fracture, treatment, guidelines, quality
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
441 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Case Manager Intervention
Arm Type
Experimental
Arm Description
Osteoporosis case-managers will identify older fracture patients in Emergency Departments and Fracture Clinics; arrange bone mineral density (BMD) tests; meet with patients to counsel them and go over their results; and then offer and prescribe bisphosphonate treatment to those with low BMD.
Arm Title
Multifaceted quality improvement intervention
Arm Type
Active Comparator
Arm Description
Active-comparator control consisting of telephone-based education for patients and treatment guidelines with reminders for family physicians
Intervention Type
Other
Intervention Name(s)
case management
Intervention Type
Other
Intervention Name(s)
Multifaceted quality improvement intervention
Primary Outcome Measure Information:
Title
Proportion of untreated patients newly starting prescription osteoporosis treatment with a bisphosphonate after their fracture
Description
Proportion of previously untreated patients (%) newly starting prescription osteoporosis treatment with a bisphosphonate within 6-months of an upper extremity fragility fracture
Time Frame
6-months
Secondary Outcome Measure Information:
Title
New Treatment Persistence
Description
Of those newly starting treatment, what proportion are still persisting with it at 1-year of followup
Time Frame
1-year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age 50 years or greater
any forearm (distal radius or ulna, "wrist") or arm (proximal humerus, "upper arm") fracture
Exclusion Criteria:
unable to give simple informed consent or unwilling to participate in the study
unable to understand, read, and converse in English
presence of pathological (e.g., cancer related) or multiple (e.g., major trauma) fractures
already treated for osteoporosis with a bisphosphonate
residence in a nursing home or from outside Edmonton
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sumit R Majumdar, MD, MPH
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Carrie Ye, MD
Organizational Affiliation
University of Alberta
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alberta Hospitals
City
Edmonton
State/Province
Alberta
ZIP/Postal Code
T6G 2B7
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
20358359
Citation
Majumdar SR, Johnson JA, Bellerose D, McAlister FA, Russell AS, Hanley DA, Garg S, Lier DA, Maksymowych WP, Morrish DW, Rowe BH. Nurse case-manager vs multifaceted intervention to improve quality of osteoporosis care after wrist fracture: randomized controlled pilot study. Osteoporos Int. 2011 Jan;22(1):223-30. doi: 10.1007/s00198-010-1212-7. Epub 2010 Apr 1.
Results Reference
background
PubMed Identifier
18299546
Citation
Majumdar SR, Johnson JA, McAlister FA, Bellerose D, Russell AS, Hanley DA, Morrish DW, Maksymowych WP, Rowe BH. Multifaceted intervention to improve diagnosis and treatment of osteoporosis in patients with recent wrist fracture: a randomized controlled trial. CMAJ. 2008 Feb 26;178(5):569-75. doi: 10.1503/cmaj.070981.
Results Reference
background
PubMed Identifier
30232538
Citation
McAlister FA, Ye C, Beaupre LA, Rowe BH, Johnson JA, Bellerose D, Hassan I, Majumdar SR. Adherence to osteoporosis therapy after an upper extremity fracture: a pre-specified substudy of the C-STOP randomized controlled trial. Osteoporos Int. 2019 Jan;30(1):127-134. doi: 10.1007/s00198-018-4702-7. Epub 2018 Sep 19.
Results Reference
derived
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C-STOP Fracture Trial
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