- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05445336
The iCARE Study: Education Modules for Fracture Prevention (iCARE)
June 27, 2025 updated by: Alexandra Papaioannou, McMaster University
The iCARE Study: An Integrated Collection of Education Modules on Fall and Fracture Prevention for Healthcare Providers
A large proportion of older adults living in long term care homes are frail and have osteoporosis.
With age, there is a gradual and progressive decline in bone quality and quantity and an increase in frailty, which is associated with increased fracture risk.
Additionally, fractures pose a significant burden to the health and quality of life of long term care residents and contribute to high healthcare costs.
Despite the high prevalence of osteoporosis, falls, and fractures in long term care, the management of osteoporosis is not optimal among long term care residents at risk of fracture.
The aim of this study is to co-design a service provision (i.e., PREVENT - Person-centred Routine Fracture PreEVENTion) with healthcare providers in long term care and to determine the feasibility of implementing PREVENT in long term care settings.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Fractures pose a significant burden on health, quality of life, and mortality of older adults in long term care (LTC) and contribute to high health care costs.
PREVENT (Person-centred Routine Fracture PreEVENTion) is a scalable model for delivering routine assessments and interventions on diet and supplements, multifactorial fall and fracture prevention strategies, and medications to long term care teams to treat residents at high risk of fracture.
The purpose of the iCARE study is to create a fall and fracture educational program (i.e., PREVENT) for LTC healthcare providers to deliver routine assessments for the management and treatment of osteoporosis.
The benefit of such a guide may help to reduce the devastating impact of fractures in older adults residing in LTC homes.
The aim of this pilot study is to: 1) determine feasibility and 2) adaptations through facilitators and barriers.
Before a larger trial can be implemented to determine the effectiveness of the PREVENT Program in practice, the iCARE study seeks to determine the feasibility of implementing PREVENT in practice and identify strategies to tailor the program to the individual long term care home and care team through design thinking solutions.
Study Type
Observational
Enrollment (Actual)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Hamilton, Ontario, Canada, N3T 5M1
- Geras Centre for Aging Research
-
-
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.
Eligibility Criteria
Ages Eligible for Study
14 years to 96 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Care planning in long term care is a collaborative effort between the resident, the long term care healthcare provider, and the resident's family/caregiver.
An internal champion will be identified to represent several long term care homes and who will help identify the five Professional Advisory Committees care teams who are the end-users of the PREVENT program.
The Professional Advisory Committee may consist of a Director of Care/Nursing Director, Medical Director, Clinical Consultant Pharmacist, and other participating members who may include dietitians, rehabilitation staff, nurses, physicians, and personal support workers.
Description
Organizational Level Inclusion Criteria:
Five long LTC homes in Ontario that
- Have a minimum of 70 residents
- Are publicly owned and private for-profit and private not-for-profit homes in both urban and rural sites
Individual Level Inclusion Criteria:
- At least one internal champion
- Five Professional Advisory Committee (PAC) care teams from five long term care homes in Ontario that provide osteoporosis care to residents.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Internal Champion & LTC Leadership Team #1 from Site #1
The internal champion and LTC leadership team of each LTC home will attend two virtual focus group sessions to help co-design the PREVENT Program educational material.
The internal champion will receive training on how to deliver the PREVENT program to the leadership team.
The internal champion/pharmacist/data analyst will receive training on how to develop an audit and feedback report on fall and fracture management.
All participants will attend an educational meeting facilitated by the internal champion who will use a combination of didactic and interactive activities.
After the educational meeting, the leadership team will complete an action and care planning report for each LTC resident at high risk of fracture.
Lastly, all participants will attend two virtual focus group sessions to discuss the successes and challenges of implementing the PREVENT program in practice.
|
PREVENT (Person-centred Routine Fracture PreEVENTion) is a scalable model for delivering routine assessments and interventions on diet and supplements, multifactorial fall and fracture prevention strategies, and medications to long term care teams to treat residents at high risk of fracture.
|
|
Internal Champion & LTC Leadership Team #2 from Site #2
The internal champion and LTC leadership team of each LTC home will attend two virtual focus group sessions to help co-design the PREVENT Program educational material.
The internal champion will receive training on how to deliver the PREVENT program to the leadership team.
The internal champion/pharmacist/data analyst will receive training on how to develop an audit and feedback report on fall and fracture management.
All participants will attend an educational meeting facilitated by the internal champion who will use a combination of didactic and interactive activities.
After the educational meeting, the leadership team will complete an action and care planning report for each LTC resident at high risk of fracture.
Lastly, all participants will attend two virtual focus group sessions to discuss the successes and challenges of implementing the PREVENT program in practice.
|
PREVENT (Person-centred Routine Fracture PreEVENTion) is a scalable model for delivering routine assessments and interventions on diet and supplements, multifactorial fall and fracture prevention strategies, and medications to long term care teams to treat residents at high risk of fracture.
|
|
Internal Champion & LTC Leadership Team #3 from Site #3
The internal champion and LTC leadership team of each LTC home will attend two virtual focus group sessions to help co-design the PREVENT Program educational material.
The internal champion will receive training on how to deliver the PREVENT program to the leadership team.
The internal champion/pharmacist/data analyst will receive training on how to develop an audit and feedback report on fall and fracture management.
All participants will attend an educational meeting facilitated by the internal champion who will use a combination of didactic and interactive activities.
After the educational meeting, the leadership team will complete an action and care planning report for each LTC resident at high risk of fracture.
Lastly, all participants will attend two virtual focus group sessions to discuss the successes and challenges of implementing the PREVENT program in practice.
|
PREVENT (Person-centred Routine Fracture PreEVENTion) is a scalable model for delivering routine assessments and interventions on diet and supplements, multifactorial fall and fracture prevention strategies, and medications to long term care teams to treat residents at high risk of fracture.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility - Recruitment Rate
Time Frame: 2 months
|
Number of long term care homes (LTCs) in Ontario recruited within two months.
Criteria for success: recruit 5 LTC homes in Ontario within 2 months
|
2 months
|
|
Feasibility - LTC home readiness and capacity
Time Frame: 1 month
|
Determine long term care home readiness and capacity to participate in the iCARE study based on a Readiness Checklist Survey.
Criteria for success: at least 75% of homes approached are ready and have the capacity to participate in the study
|
1 month
|
|
Feasibility - Length of time to complete PREVENT Program
Time Frame: 4 months
|
Length of time for participants to implement the PREVENT Program
|
4 months
|
|
Feasibility - Logistics of linking data (Yes/No format)
Time Frame: 4 months
|
Determine the logistics of linking MDS 2.0 data with pharmaceutical database data at the resident level.
This will be assessed by a "yes" or "no" (i.e., Feasible - Yes vs. Feasible - No)
|
4 months
|
|
Fidelity of delivering the PREVENT program
Time Frame: 4-6 months
|
Determine the fidelity of delivering the PREVENT program.
Criteria for success: ≥ 80% on the fidelity checklist.
|
4-6 months
|
|
Feasibility - Number of Questions Completed
Time Frame: 4 months
|
The number of questions answered by the participants for each questionnaire.
Criteria for success is 80% of questions are completed.
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Changes in Prescribing Habits
Time Frame: 4-6 months
|
To determine if appropriate prescribing habits change after the educational session.
The criteria for success is a 10% improvement in prescribing habits.
This will be measured by the number of prescriptions per number of residents at high risk of fracture pre- vs. post-intervention.
|
4-6 months
|
|
Adaptations to PREVENT Program
Time Frame: 4-6 months
|
To determine adaptations to the PREVENT program by facilitating two 1.5-hour focus group sessions (semi-structured interviews) with the leadership team to 1) discuss facilitators of and barriers to implementing the PREVENT program and 2) make necessary changes to the PREVENT program/educational material catered to the individual LTC home.
|
4-6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Alexandra Papaioannou, MD, MSc, FRCP(c), FACP, McMaster University
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 Major Dates
Study Start (Actual)
July 30, 2022
Primary Completion (Actual)
August 15, 2023
Study Completion (Actual)
August 15, 2023
Study Registration Dates
First Submitted
January 28, 2022
First Submitted That Met QC Criteria
June 30, 2022
First Posted (Actual)
July 6, 2022
Study Record Updates
Last Update Posted (Estimated)
July 1, 2025
Last Update Submitted That Met QC Criteria
June 27, 2025
Last Verified
December 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 14463
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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