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Strategies to Improve Bone Health in Men on ADT

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Healthy bones pamphlet
Bone Health Care Coordinator
Letter to GP
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prostate Cancer focused on measuring Prostate cancer, Androgen deprivation therapy, Bone health, Bone mineral density

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

Commencing or planning to continue ADT for a least 6 months 50 years or older English fluency Life expectancy >6 months

Exclusion Criteria:

Prior Bone Mineral Density test within 2 years Prior visit at Osteoporosis Clinic within 2 years

Sites / Locations

  • Princess Margaret Cancer Centre

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Active Comparator

No Intervention

Arm Label

Healthy bones pamphlet, letter to GP

Healthy bones pamphlet, Bone Health Care Coordinator

Usual care

Arm Description

Strategy 1: Written educational material to patient and GP

Strategy 2: Written educational material to patient and counseling from a Bone Health Care Coordinator

Control group gets usual care from their oncologist.

Outcomes

Primary Outcome Measures

Patient/physician satisfaction
Satisfaction will be measured with 5-point Likert scale ranging from poor to excellent and administered to patient, PC clinician, and General Physician
Adherence rate
Adherence to following through on recommendations/referrals related to study intervention and clinical outcomes.
Recruitment rate
Enrolled patients divided by approached eligible patients, and reasons for both ineligibility and refusal as documented in logs.
Retention rate
Proportion of patients available for follow-up outcome assessment.
BMD ordering
Rate of Bone Mineral Density ordering

Secondary Outcome Measures

Full Information

First Posted
January 20, 2014
Last Updated
March 20, 2018
Sponsor
University Health Network, Toronto
Collaborators
Canadian Cancer Society (CCS)
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1. Study Identification

Unique Protocol Identification Number
NCT02043236
Brief Title
Strategies to Improve Bone Health in Men on ADT
Official Title
A Phase II RCT of Strategies to Improve Bone Health in Men on ADT
Study Type
Interventional

2. Study Status

Record Verification Date
March 2018
Overall Recruitment Status
Completed
Study Start Date
November 2013 (Actual)
Primary Completion Date
December 31, 2017 (Actual)
Study Completion Date
December 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
Canadian Cancer Society (CCS)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a phase II randomized controlled trial (RCT) of 2 strategies to improve bone health in men receiving androgen deprivation therapy (ADT).
Detailed Description
In this RCT the investigators are comparing 2 strategies to improve bone health to usual care. Strategy 1 - Patient and physician-specific written educational material. Pilot-tested customized written educational material about bone health for men on ADT will be used for this study. A customized letter will be prepared for the patient's primary care physician, with specific advice and recommendations for the targeted strategies. Both pamphlet and letter will include a list of additional resources. Strategy 2 - patient written material and a bone health care coordinator (BHCC). The same written patient material as in strategy 1 will be used, along with a BHCC who will follow the approach of successful studies and contact the patient by phone or arrange an in-person visit at the hospital if preferred by the patient. The BHCC will also encourage the patient to pursue a bone mineral density test (BMD) with their physician and adopt bone-appropriate diet, lifestyle, and supplement intake recommendations, and will follow up with the patient at least twice over the next 3 months to facilitate behavioural changes and BMD ordering. Counselling sessions are short, typically <15 min. The BHCC will also contact the patient's physician to help facilitate BMD testing. Time points in the study are baseline, 3-month follow up, and 6-month follow up. Control group The control group consists of a wait-list control for 6 months, during which no specific recommendations or interventions will be made by the study team. Prostate Cancer (PC) clinicians can still provide usual care. At the end of 6 months, control group participants will be referred to the Osteoporosis Clinic at the University Health Network.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate cancer, Androgen deprivation therapy, Bone health, Bone mineral density

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
159 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Healthy bones pamphlet, letter to GP
Arm Type
Active Comparator
Arm Description
Strategy 1: Written educational material to patient and GP
Arm Title
Healthy bones pamphlet, Bone Health Care Coordinator
Arm Type
Active Comparator
Arm Description
Strategy 2: Written educational material to patient and counseling from a Bone Health Care Coordinator
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
Control group gets usual care from their oncologist.
Intervention Type
Behavioral
Intervention Name(s)
Healthy bones pamphlet
Other Intervention Name(s)
Building strong bones
Intervention Description
written educational material
Intervention Type
Behavioral
Intervention Name(s)
Bone Health Care Coordinator
Other Intervention Name(s)
BHCC
Intervention Description
The Bone Health Care Coordinator reviews educational materials with participant and facilitates ordering BMD.
Intervention Type
Behavioral
Intervention Name(s)
Letter to GP
Intervention Description
The letter to the General Practitioner contains information about the study, recommendations for bone health, guidelines of Osteoporosis Canada, and the identical educational material that the participant received.
Primary Outcome Measure Information:
Title
Patient/physician satisfaction
Description
Satisfaction will be measured with 5-point Likert scale ranging from poor to excellent and administered to patient, PC clinician, and General Physician
Time Frame
6 months
Title
Adherence rate
Description
Adherence to following through on recommendations/referrals related to study intervention and clinical outcomes.
Time Frame
6 months
Title
Recruitment rate
Description
Enrolled patients divided by approached eligible patients, and reasons for both ineligibility and refusal as documented in logs.
Time Frame
6 months
Title
Retention rate
Description
Proportion of patients available for follow-up outcome assessment.
Time Frame
6 months
Title
BMD ordering
Description
Rate of Bone Mineral Density ordering
Time Frame
6 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Commencing or planning to continue ADT for a least 6 months 50 years or older English fluency Life expectancy >6 months Exclusion Criteria: Prior Bone Mineral Density test within 2 years Prior visit at Osteoporosis Clinic within 2 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shabbir Alibhai, MD
Organizational Affiliation
UHN
Official's Role
Principal Investigator
Facility Information:
Facility Name
Princess Margaret Cancer Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5T 2M9
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
29211305
Citation
Alibhai SMH, Breunis H, Timilshina N, Hamidi MS, Cheung AM, Tomlinson GA, Manokumar T, Samadi O, Sandoval J, Durbano S, Warde P, Jones JM. Improving bone health in men with prostate cancer receiving androgen deprivation therapy: Results of a randomized phase 2 trial. Cancer. 2018 Mar 15;124(6):1132-1140. doi: 10.1002/cncr.31171. Epub 2017 Dec 6.
Results Reference
derived

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Strategies to Improve Bone Health in Men on ADT

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