A Web-based Peer Navigation Program for Men With Prostate Cancer
Primary Purpose
Prostate Cancer
Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Peer navigation
Active wait list control
Sponsored by
About this trial
This is an interventional supportive care trial for Prostate Cancer focused on measuring prostate cancer, navigation, peer support, web-based, patient activation
Eligibility Criteria
Inclusion Criteria:
- Has been diagnosed with local, locally advanced or stable metastatic PC.
- Has recently completed treatment within 3 months
- Has an email address OR is willing to create one.
- Can read and speak English.
Exclusion Criteria:
- Has been diagnosed with advanced metastatic disease.
- Is receiving palliative care.
- Is not willing to be randomized.
Sites / Locations
- Vancouver General Hospital
- BC Cancer - Vancouver
- Queen Elizabeth II Health Sciences Centre
- Cape Breton Regional Hospital
- Princess Margaret Cancer CentreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
Intervention
Active Waitlist Control
Arm Description
Participants assigned to the intervention arm will receive the True North Peer Navigation intervention.
Participants assigned to the control arm will receive usual care and access to an online health resource library. After completion of the study, they will receive the True North Peer Navigation intervention.
Outcomes
Primary Outcome Measures
Change in Patient Activation at 3 months
The primary outcome will be change in Patient Activation from baseline to 3 months. Patient Activation will be measured using the Patient Activation Measure (PAM). Higher scores represent a better outcome.
Secondary Outcome Measures
Change in Patient Activation at 6 months
Change in Patient Activation from baseline to 6 months will be assessed.Patient Activation will be measured using the Patient Activation Measure (PAM). Higher scores represent a better outcome.
Change in Supportive Care Needs
Change in Supportive Care Needs from baseline will be assessed at 3 months and 6 months separately. Supportive Care Needs will be measured with the 34-item Supportive Care Needs Survey-Short Form (SCNS-SF) with a 7-item prostate cancer add-on module. Higher scores represent a worse outcome.
Change in Health-Related Quality of Life
Change in health-related quality of life from baseline will be assessed at 3 months and 6 months separately. Health-related quality of life will be measured with the European Quality of Life, 5 Dimensions, 5 Levels (EQ-5D-5L) overall utility score. Higher scores represent a worse outcome.
Change in Prostate Cancer Quality of Life
Change in Prostate Cancer Specific Quality of Life from baseline will be measured t 3 months and 6 months separately. Prostate Cancer Specific Quality of Life will be measured using the overall Patient-Oriented Prostate Utility Scale (PORPUS) score. Higher scores represent a worse outcome.
Change in Anxiety
Change in Anxiety from baseline will be assessed at 3 months and 6 months separately. Anxiety will be measured using the Generalized Anxiety Disorder scale (GAD-7). Higher scores represent a worse outcome.
Change in Depression
Change in Depression from baseline will be assessed at 3 months and 6 months separately. Depression will be measured using the depression module of the Patient Health Questionnaire (PHQ-9). Higher scores represent a worse outcome.
Change in Social Support
Change in Social Support from baseline will be measured at 3 months and 6 months separately. Social Support will be measured using the Enriched Social Support Scale, a multidimensional measure of perceived social support (ESSI). Higher scores represent a worse outcome.
Change in Fear of Cancer Recurrence
Change in Fear of Cancer Recurrence from baseline will be assessed at 3 months and 6 months separately. Fear of Cancer Recurrence will be measured using the Fear of Cancer Recurrence Inventory -Short Form Scale (FCRI-SF). Higher scores represent a worse outcome.
Full Information
NCT ID
NCT05041504
First Posted
August 10, 2021
Last Updated
July 26, 2023
Sponsor
University Health Network, Toronto
Collaborators
University of British Columbia, Dalhousie University, University of Toronto, Canadian Cancer Society (CCS), Canadian Partnership Against Cancer, Movember Foundation, Walnut Foundation, Prostate Cancer Support - Toronto, Prostate Cancer Group - Burnaby
1. Study Identification
Unique Protocol Identification Number
NCT05041504
Brief Title
A Web-based Peer Navigation Program for Men With Prostate Cancer
Official Title
A Web-based Peer Navigation Program for Men With Prostate Cancer: A Hybrid Effectiveness-Implementation Trial
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 13, 2022 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
March 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
University of British Columbia, Dalhousie University, University of Toronto, Canadian Cancer Society (CCS), Canadian Partnership Against Cancer, Movember Foundation, Walnut Foundation, Prostate Cancer Support - Toronto, Prostate Cancer Group - Burnaby
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
One in nine Canadian men will be diagnosed with prostate cancer (PC) in their lifetime. Although all treatment options can be effective in controlling the disease, treatment side effects such as problems with erections and controlling the bladder can significantly affect men's quality of life. Many men with PC say they do not get relevant information and emotional support, and experience gaps in care when dealing with these difficult issues. Previous studies have shown that cancer patient navigation improves access to care and support, and reduces healthcare costs. The investigators developed True North Peer Navigation - a peer navigation program for men with PC and a peer navigator training course. Men are matched online with a trained peer navigator who provides practical information and emotional support through the cancer journey. A pilot evaluation showed that it is highly acceptable to patients and peer navigators, and improves patient quality of life, social support and ability to manage their health. In this study, the investigators will conduct a randomized controlled trial of the True North Peer Navigation program in cancer centres in Ontario, British Columbia and Nova Scotia. Patients will be randomly assigned to receive True North Peer Navigation or an active wait list control consisting of usual care with access to information on the True North Peer Navigation website. The investigators will evaluate the effect of the True North Peer Navigation program on patient outcomes such as their ability to take a more active role in their health, quality of life, social support and use of health care services. In addition, the investigators will evaluate how True North Peer Navigation was implemented, the experiences patients and peer navigators, the factors that make it easier or harder for people to deliver the program to patients in different settings, as well as the cost of delivering the program, which will help us learn how to spread the program across the country.
Detailed Description
Background: Prostate cancer (PC) is a highly prevalent condition affecting 1 in 9 Canadian men. While the 5-year survival rate for PC is 93%, treatment-related side effects, such as sexual dysfunction and urinary incontinence, can significantly affect quality of life. Men with PC lack access to relevant information and emotional support, and report gaps in supportive care when dealing with these difficult issues. Previous research has shown that cancer patient navigation improves the timeliness of care and support, and reduces healthcare costs. Engaging volunteer cancer survivors as navigators is less costly, provides peer support, and benefits the navigator by improving their psychosocial health. The investigators developed True North Peer Navigation - an evidence-based peer navigation program for men with PC and a competency-based peer navigator training course. Men are matched online with a trained peer navigator who assesses needs and barriers to care, provides practical, informational, and emotional support, and empowers them to take a proactive role in their health. A pilot study showed True North Peer Navigation is highly acceptable to patients and peer navigators, and associated with improvements in quality of life, social support and patient activation to manage health.
Aim: This project aims to advance knowledge on the effectiveness and implementation of a web-based peer navigation program for men after treatment for PC.
Specific Objectives:
To determine the effect of True North Peer Navigation on patient outcomes in men with PC; and
To evaluate the delivery of True North Peer Navigation in terms of fidelity, cost, and the experiences of patients and peer navigators, and to identify barriers and facilitators to its implementation in oncology settings.
Methods: Guided by the SPOR Patient Engagement Framework, the investigators will conduct a type-1 hybrid effectiveness-implementation study at cancer centres in Ontario, British Columbia and Nova Scotia. For objective 1, the investigators will conduct a pragmatic randomized controlled trial to evaluate the impact of True North Peer Navigation compared to an active wait list control on patient activation (primary) and needs, quality of life, anxiety, depression, fear of recurrence, social support, and access to services (secondary). Two hundred and forty patients (n=120 per arm) with PC will be recruited after treatment. Outcomes will be assessed at baseline (T0), 3-months (T1) and 6-months (T2). Objective 2 will involve a mixed-method process evaluation to investigate implementation fidelity, patient and navigator experiences, and cost-effectiveness of True North Peer Navigation, and to assess implementation barriers and facilitators with stakeholders informed by the Consolidated Framework for Implementation Research and the Theoretical Domains Framework.
Significance: True North Peer Navigation is an innovative solution to an important service gap in the lives of men with PC. This study has the potential to generate important evidence and strategies to support the implementation of peer navigation programs to improve the health outcomes of men with PC in Canada.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
prostate cancer, navigation, peer support, web-based, patient activation
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This is a 2-arm pragmatic randomized controlled trial with an active wait-list control, and an embedded process evaluation. Participants in the intervention group will receive the True North Peer Navigation intervention. Participants in the active control group will receive access to an online health resource library and will be offered the True North Peer Navigation intervention after study completion.
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
240 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Participants assigned to the intervention arm will receive the True North Peer Navigation intervention.
Arm Title
Active Waitlist Control
Arm Type
Other
Arm Description
Participants assigned to the control arm will receive usual care and access to an online health resource library. After completion of the study, they will receive the True North Peer Navigation intervention.
Intervention Type
Behavioral
Intervention Name(s)
Peer navigation
Other Intervention Name(s)
True North Peer Navigation
Intervention Description
Participants in the intervention group will receive ongoing support from a trained peer navigator for 3 months after completing treatment for prostate cancer via the True North Peer Navigation website. Participants will be matched with a trained peer navigator who assesses needs and barriers to care, provides practical, informational, and emotional support, and empowers them to take a proactive role in their health. Participants will also have access to a health resource library on the True North Peer Navigation website that contains local and national resources about prostate cancer.
Intervention Type
Other
Intervention Name(s)
Active wait list control
Other Intervention Name(s)
Web-based educational wait list control
Intervention Description
Participants in the active wait list control group will receive usual care and access to a health resource library on the True North Peer Navigation website that contains local and national resources about prostate cancer. After completion of the study, patients in the active wait list control group will be matched with a peer navigator.
Primary Outcome Measure Information:
Title
Change in Patient Activation at 3 months
Description
The primary outcome will be change in Patient Activation from baseline to 3 months. Patient Activation will be measured using the Patient Activation Measure (PAM). Higher scores represent a better outcome.
Time Frame
0, 3 months
Secondary Outcome Measure Information:
Title
Change in Patient Activation at 6 months
Description
Change in Patient Activation from baseline to 6 months will be assessed.Patient Activation will be measured using the Patient Activation Measure (PAM). Higher scores represent a better outcome.
Time Frame
0, 6 months
Title
Change in Supportive Care Needs
Description
Change in Supportive Care Needs from baseline will be assessed at 3 months and 6 months separately. Supportive Care Needs will be measured with the 34-item Supportive Care Needs Survey-Short Form (SCNS-SF) with a 7-item prostate cancer add-on module. Higher scores represent a worse outcome.
Time Frame
0, 3, 6 months
Title
Change in Health-Related Quality of Life
Description
Change in health-related quality of life from baseline will be assessed at 3 months and 6 months separately. Health-related quality of life will be measured with the European Quality of Life, 5 Dimensions, 5 Levels (EQ-5D-5L) overall utility score. Higher scores represent a worse outcome.
Time Frame
0, 3, 6 months
Title
Change in Prostate Cancer Quality of Life
Description
Change in Prostate Cancer Specific Quality of Life from baseline will be measured t 3 months and 6 months separately. Prostate Cancer Specific Quality of Life will be measured using the overall Patient-Oriented Prostate Utility Scale (PORPUS) score. Higher scores represent a worse outcome.
Time Frame
0, 3, 6 months
Title
Change in Anxiety
Description
Change in Anxiety from baseline will be assessed at 3 months and 6 months separately. Anxiety will be measured using the Generalized Anxiety Disorder scale (GAD-7). Higher scores represent a worse outcome.
Time Frame
0, 3, 6 months
Title
Change in Depression
Description
Change in Depression from baseline will be assessed at 3 months and 6 months separately. Depression will be measured using the depression module of the Patient Health Questionnaire (PHQ-9). Higher scores represent a worse outcome.
Time Frame
0, 3, 6 months
Title
Change in Social Support
Description
Change in Social Support from baseline will be measured at 3 months and 6 months separately. Social Support will be measured using the Enriched Social Support Scale, a multidimensional measure of perceived social support (ESSI). Higher scores represent a worse outcome.
Time Frame
0, 3, 6 months
Title
Change in Fear of Cancer Recurrence
Description
Change in Fear of Cancer Recurrence from baseline will be assessed at 3 months and 6 months separately. Fear of Cancer Recurrence will be measured using the Fear of Cancer Recurrence Inventory -Short Form Scale (FCRI-SF). Higher scores represent a worse outcome.
Time Frame
0, 3, 6 months
Other Pre-specified Outcome Measures:
Title
Quality-adjusted life year
Description
An estimation of the combined health utility values derived from responses from the European Quality of Life, 5 Dimensions, 5 Levels (EQ-5D-5L) and length of life experienced by patient, between measurement time points.
Time Frame
0,3,6 months
Title
Total healthcare costs
Description
The total cost of publicly funded healthcare utilization (outside of delivery of the intervention) by patient while enrolled in the study. Number of times patient accessed publicly funded healthcare resources while enrolled in the study will be estimated based on the data gathered from the Health System Service Utilization Inventory (HSSUI). Resource use volumes will be used to micro-cost resource use costs such as physician care, allied health professional care, hospital care and pharmaceuticals.
Time Frame
3,6 months
Title
Intervention cost
Description
Incremental cost of the intervention (i.e., delivery of the peer navigation program not related to volunteer time, such as administrative costs, training costs, and overhead costs) will be estimated per patient.
Time Frame
3 years
10. Eligibility
Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Has been diagnosed with local, locally advanced or stable metastatic PC.
Has recently completed treatment within 3 months
Has an email address OR is willing to create one.
Can read and speak English.
Exclusion Criteria:
Has been diagnosed with advanced metastatic disease.
Is receiving palliative care.
Is not willing to be randomized.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jackie Bender, PhD
Phone
416-581-8606
Email
Jackie.Bender@uhnresearch.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jackie Bender, PhD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 1M9
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arminee Kazanjian, PhD
Phone
604-822-4618
Email
arminee.kazanjian@ubc.ca
First Name & Middle Initial & Last Name & Degree
Andrea Vodermaier, PhD
Phone
604-827-1831
Email
andrea.vodermaier@ubc.ca
First Name & Middle Initial & Last Name & Degree
Ryan Flannigan, MD
Facility Name
BC Cancer - Vancouver
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 4E6
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arminee Kazanjian, PhD
Phone
604-822-4618
Email
arminee.kazanjian@ubc.ca
First Name & Middle Initial & Last Name & Degree
Andrea Vodermaier, PhD
Phone
604-827-1831
Email
andrea.vodermaier@ubc.ca
First Name & Middle Initial & Last Name & Degree
Michael McKenzie, MD
Facility Name
Queen Elizabeth II Health Sciences Centre
City
Halifax
State/Province
Nova Scotia
ZIP/Postal Code
B3H 2Y9
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Robin Urquhart, PhD
Phone
902-473-7290
Email
Robin.Urquhart@nshealth.ca
First Name & Middle Initial & Last Name & Degree
Samantha Radford, MSc
Phone
902-473-7290
Email
Samantha.Radford@nshealth.ca
First Name & Middle Initial & Last Name & Degree
David Bowes, MD
First Name & Middle Initial & Last Name & Degree
Ricardo Rendon, MD
Facility Name
Cape Breton Regional Hospital
City
Sydney
State/Province
Nova Scotia
ZIP/Postal Code
B1P 1P3
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Robin Urquhart, PhD
Phone
902-473-7290
Email
Robin.Urquhart@nshealth.ca
First Name & Middle Initial & Last Name & Degree
Samantha Radford, MSc
Phone
902-473-7290
Email
Samantha.Radford@nshealth.ca
Facility Name
Princess Margaret Cancer Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2C1
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jackie Bender, PhD
Phone
416-581-8606
Email
jackie.bender@uhnresearch.ca
First Name & Middle Initial & Last Name & Degree
Jackie Bender, PhD
First Name & Middle Initial & Last Name & Degree
Peter Chung, MD
First Name & Middle Initial & Last Name & Degree
Antonio Finelli, MD
First Name & Middle Initial & Last Name & Degree
Rebecca Hancock-Howard, PhD
First Name & Middle Initial & Last Name & Degree
Jennifer Jones, PhD
First Name & Middle Initial & Last Name & Degree
Amy-Zhihui Liu, PhD
First Name & Middle Initial & Last Name & Degree
Andrew Matthew, PhD, C.Psych
First Name & Middle Initial & Last Name & Degree
Nathan Perlis, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32613373
Citation
Bender JL, Flora PK, Milosevic E, Soheilipour S, Maharaj N, Dirlea M, Parvin L, Matthew A, Kazanjian A. Training prostate cancer survivors and caregivers to be peer navigators: a blended online/in-person competency-based training program. Support Care Cancer. 2021 Mar;29(3):1235-1244. doi: 10.1007/s00520-020-05586-8. Epub 2020 Jul 2.
Results Reference
background
PubMed Identifier
31616997
Citation
Flora PK, Bender JL, Miller AS, Parvin L, Soheilipour S, Maharaj N, Milosevic E, Matthew A, Kazanjian A. A core competency framework for prostate cancer peer navigation. Support Care Cancer. 2020 Jun;28(6):2605-2614. doi: 10.1007/s00520-019-05059-7. Epub 2019 Oct 15.
Results Reference
background
Citation
Maharaj N, Soheilipour S, Bender JL, Kazanjian A. Understanding Prostate Cancer Patients and Caregivers Support Needs: How Do They Manage Living with Cancer? Illness, Crisis & Loss. 2018; April 5:51-73.
Results Reference
background
Links:
URL
https://peernavigation.truenth.ca/start/pcc-i8/index.html
Description
TrueNORTH Peer Navigation intervention website
Learn more about this trial
A Web-based Peer Navigation Program for Men With Prostate Cancer
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