Effectiveness of RISE as a Community-Based Stand-Alone Elder Abuse Intervention Model
Implementing and Testing RISE: Addressing a Gap in Community-Based Elder Abuse Response Intervention
1 other identifier
interventional
114
1 country
2
Brief Summary
The goal of this randomized clinical trial is to learn if the RISE intervention can improve the well being of older adults who are at risk of or experiencing elder abuse or self-neglect (EASN). The main questions it aims to answer are:
- Do older adults who go through the RISE intervention experience improvements in their well-being?
- Are older adults who go through RISE satisfied with this program? Researchers will compare older adults who receive a one-time consultation and resource-sharing service to older adults who receive the multi-session RISE intervention to see if there are differences in their well-being. Participants will engage in the RISE intervention over several months by telephone or in person to work on goals that are designed to reduce the risk of elder abuse or self-neglect, and they will participate in telephone-based surveys at three different times.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Oct 2023
Typical duration for not_applicable
2 active sites
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
Study Start
First participant enrolled
October 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 31, 2025
CompletedFirst Submitted
Initial submission to the registry
April 7, 2026
CompletedFirst Posted
Study publicly available on registry
April 14, 2026
CompletedApril 14, 2026
April 1, 2026
1.8 years
April 7, 2026
April 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Total Life Satisfaction
A life satisfaction index comprising 7 key EASN intervention targets each measured on a Likert scale from 1 (never) to 4 (always), including satisfaction with: physical safety, overall health, social life, mood, financial situation, housing situation, and family life. This index is measured as a part of a telephone-based survey across three time points: baseline, 3-month follow-up, and 6-month follow-up.
From enrollment to 6 months
Secondary Outcomes (7)
PROMIS Perceived Stress
From enrollment to 6 months
PROMIS General Self-Efficacy
From enrollment to 6 months
PROMIS Social Interaction Self-Efficacy
From enrollment to 6 months
PROMIS Emotional Social Support
From enrollment to 6 months
PROMIS Information Social Support
From enrollment to 6 months
- +2 more secondary outcomes
Study Arms (2)
Treatment Group
EXPERIMENTALRISE Model
Control Group
ACTIVE COMPARATORBrief Consultation and Resource Sharing
Interventions
RISE works with cases involving older adults who are at risk of (prevention) or experiencing (response intervention) EASN. The model operates at Relational, Individual, Social, and Environmental levels and, through its core modalities, the intervention seeks to Repair Harm (restorative approaches), Inspire Change (motivational interviewing), Support Connection (teaming), and Empower Choice (supported decision making). RISE intervenes with the individual older adult EASN victim and alleged harmer (when appropriate), their relationship, and strengthens their informal and formal social supports.
A brief 45-minute telephone consultation involving active listening skills and referral resource sharing
Eligibility Criteria
You may qualify if:
- Age 60+
- At risk of or experiencing EASN
- Cognitive capacity
- Lives in community
You may not qualify if:
- Lives in long-term care setting
- Cognitive impairment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- RISE Collaborativelead
- Public Health Agency of Canada (PHAC)collaborator
- University of Torontocollaborator
- Social Sciences and Humanities Research Council of Canadacollaborator
Study Sites (2)
Elder Abuse Prevention Ontario
Toronto, Ontario, M2K 2Y5, Canada
Factor-Inwentash Faculty of Social Work
Toronto, Ontario, M5S 1V4, Canada
Related Publications (4)
MacNeil A, Connolly MT, Salvo E, Kimball PF, Rogers G, Lewis S, Burnes D. Use of Motivational Interviewing by Advocates in the Context of an Elder Abuse Response Intervention: The RISE Project. J Fam Violence. 2023 Apr 27:1-11. doi: 10.1007/s10896-023-00563-1. Online ahead of print.
PMID: 37358985BACKGROUNDCampo-Tena L, Herbst JH, Choo WY, Burnes D, Couture M, Estebsari F, Kafando CSL, Rouamba G, Simbreni MM, Yan E, Yon Y, Mikton C. Seven candidate interventions to address abuse of older people. Age Ageing. 2025 Aug 29;54(9):afaf248. doi: 10.1093/ageing/afaf248.
PMID: 40921050BACKGROUNDBurnes D, Connolly MT, Salvo E, Kimball PF, Rogers G, Lewis S. RISE: A Conceptual Model of Integrated and Restorative Elder Abuse Intervention. Gerontologist. 2023 Jul 18;63(6):966-973. doi: 10.1093/geront/gnac083.
PMID: 35705108BACKGROUNDLewis S, Connolly MT, Salvo E, Kimball PF, Rogers G, MacNeil A, Burnes D. Effect of an elder abuse and self-neglect intervention on repeat investigations by adult protective services: RISE project. J Am Geriatr Soc. 2023 Nov;71(11):3403-3412. doi: 10.1111/jgs.18506. Epub 2023 Jul 10.
PMID: 37427825BACKGROUND
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
April 7, 2026
First Posted
April 14, 2026
Study Start
October 1, 2023
Primary Completion
July 31, 2025
Study Completion
July 31, 2025
Last Updated
April 14, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- SAP, ANALYTIC CODE
- Time Frame
- Beginning 6 months and ending 3 years after the publication of results
- Access Criteria
- Researchers who are affiliated with an accredited post-secondary institution may request access to de-identified quantitative or qualitative data through written proposal to the principal investigator, which describes aims and analytic plan. The proposal will be reviewed by a RISE Collaborative research team and approval will be subject to an inter-institutional data sharing agreement.
De-identified individual participant data (IPD), limited to data used in the results publication, is available to other researchers, following publication, who are affiliated with an accredited post-secondary institution upon request to the principal investigator.