RecruitingNot ApplicableNCT07475039

Project HOPEFUL: A PN-RCT With Implementation Science

Project HOPEFUL (Helping Older PErsons Find Useful Links): Replicating a Partially Nested Randomized Control Trial With Implementation Science


Sponsor

University of Florida

Enrollment

400 participants

Start Date

Sep 5, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This PN-RCT replicates and evaluates an 8-week warm calling treatment (i.e. caring contacts) delivered to older adults receiving home and community-based services (HCBS; classified as "homebound") in 20-30 minute call "dosages", across 3 conditions, while adding in implementation science measures at multiple levels. Conditions include 2 treatment (i.e. treatment provided by helpers trained in a standardized and manualized Belongingness and Empathy training grounded in narrative reminiscence and the befriending literature (BE condition), and treatment provided by helpers trained in BE + a standardized, manualized, and evidence based suicide intervention training, the Aging Variant of LivingWorks ASIST (BE + ASIST condition), and 1 control (no treatment during the trial; opportunity to receive treatment after the 8 weeks). At the conclusion of treatment, acceptability, appropriateness, feasibility, useability, and sustainability of the program will be evaluated by interventionists, senior center leadership, and regional leadership.


Eligibility

Min Age: 55 Years

Plain Language Summary

Simplified for easier understanding

Project HOPEFUL is a study testing a program designed to reduce loneliness and improve mental well-being in older adults (65+) who receive home or community-based services like meal delivery. The program involves regular warm, supportive phone calls from trained community helpers. **You may be eligible if...** - You are 65 years or older - You receive services through an aging support network (such as home-delivered meals or congregate meal programs) - You are willing and able to participate in study activities - You are affiliated with one of the partnering aging organizations **You may NOT be eligible if...** - You have been diagnosed with dementia, significant cognitive impairment, or hearing problems that would prevent phone conversations - You are already participating in another similar phone-based behavioral program Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALStandardized and manualized warm calls from providers trained in the BE training

Weekly call dosages averaging 20-30 minutes each, for 8 weeks duration; with a 6 month follow up.

BEHAVIORALStandardized and manualized warm calls from providers trained in the BE training + ASIST training

Weekly call dosages averaging 20-30 minutes each, for 8 weeks duration; with a 6 month follow up.


Locations(1)

University of Florida

Gainesville, Florida, United States

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NCT07475039


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