Perceived Burdensomeness

2

Review clinical trials related to Perceived Burdensomeness. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Evaluation of a Brief, Scalable Module to Mitigate Suicidal Ideation Among Youth (Phase 2)

This project embeds the "Give to Others" (GO) talk therapy module in a standard, outpatient therapy protocol to demonstrate target engagement in the context of ongoing clinical care and testing the ability of the GO module to engage the target in a rigorous randomized controlled trial (RCT) of the intervention. We will target perceived burdensomeness (PB) among 80 clinic-referred youths (ages 12-17) who experience subacute suicidal ideation (SI; i.e., positive suicide risk screen; stable safety status).

Participants needed: 80
Trial details
Age: 12-17Biological sex: AllType: InterventionalSponsor: Florida International UniversityUpdated: Sep 29, 2026Locations: 1
Eligibility criteria

be between ages 12 and 17 years [+4]

have cognitive impairment or developmental delay which does not allow for the co... [+2]

Status: Recruiting

Project HOPEFUL: A PN-RCT With Implementation Science

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.

Participants needed: 400
Trial details
Age: 55+Biological sex: AllType: InterventionalSponsor: University of FloridaUpdated: Mar 16, 2026Locations: 1
Eligibility criteria

Provision of verbal informed consent [+12]

Had a dementia diagnosis, or another form of cognitive impairment, and/or hearin... [+5]