A Community Health Education Intervention for Increasing Community-driven Actions to Reduce the Cancer Burden in Western New York
I Can Join the Fight Against Cancer: An Intervention to Programmatically Build Grassroots Actions to Reduce the Cancer Burden
2 other identifiers
interventional
200
1 country
1
Brief Summary
This clinical trial evaluates a community health education intervention (I CAN) for increasing community-driven actions to reduce the cancer burden in Western New York. Engaging community members is a critical component of designing impactful programs to reduce the cancer burden. Leaders at the national, state, and local levels have all called for more community partnerships and engagement in design of health intervention and policies. The I CAN intervention is a workshop that includes a presentation outlining key concepts related to social network processes and the cancer burden in Western New York, a structured skill-building activity, and then empowering and motivating activities meant to cultivate momentum and excitement for action. This community health education intervention may be able to provide a formalized process for empowering and facilitating community members to take steps to reduce the community cancer burden.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable healthy
Started Nov 2024
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 1, 2024
CompletedFirst Posted
Study publicly available on registry
November 8, 2024
CompletedStudy Start
First participant enrolled
November 16, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
November 15, 2026
March 13, 2026
March 1, 2026
2 years
November 1, 2024
March 11, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Demand
Feasibility will be assessed through demand, which will be evaluated as the number of people enrolled and the demographics of participants. Descriptive analyses will be used.
Up to 2 years
Practicality
Practicality will be assessed through the percentage of participants who complete different aspects of the intervention. Descriptive analyses will be used.
Up to 2 years
Acceptability
Acceptability will be examined through post-intervention measures, including the Acceptability of Intervention Measure, Intervention Appropriateness Measure, and Feasibility of Intervention Measure. Descriptive analyses will be used.
UP to 2 years
Study Arms (1)
Prevention (I CAN intervention)
EXPERIMENTALParticipants attend an I CAN intervention workshop over 2 hours.
Interventions
Receive I CAN intervention
Eligibility Criteria
You may qualify if:
- Being over 18 years old
- Able to participate in English
You may not qualify if:
- Unwilling or unable to follow protocol requirements
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Roswell Park Cancer Institute
Buffalo, New York, 14263, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Elizabeth Bouchard
Roswell Park Cancer Institute
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 1, 2024
First Posted
November 8, 2024
Study Start
November 16, 2024
Primary Completion (Estimated)
November 15, 2026
Study Completion (Estimated)
November 15, 2026
Last Updated
March 13, 2026
Record last verified: 2026-03