Development and Preliminary Testing of a "Papageno"-Story Interview Intervention- Aim 3

NCT06842667 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 506

Last updated 2025-10-09

No results posted yet for this study

Summary

The purpose of this study is to determine the effects of a short "Papageno story" video of a compilation of interviews on proximal risk factors for suicide. The researchers believe that the intervention may increase protective factors related to suicide.

Conditions

  • Suicide Prevention

Interventions

BEHAVIORAL

Papageno video

The intervention will be a video (14 min 13 sec in length) of a series of clips from the "Papageno" interviews developed during the pilot phase of this project. The decision to combine the videos and shorten the total length of the video was based on the feedback we received during the acceptability and feasibility phase of this study. Interviewees were asked questions about a time in their life when they came close to suicide but found non-suicide alternatives (their "Papageno" story).

BEHAVIORAL

Control video

The control condition will involve viewing a mental health education video (12 min 14 sec in length) created by our team. It is a simple informational video, aimed at psychoeducation about suicide and safety promotion. It includes a list of mental health and crisis resources. Both videos are interview-style.

Sponsors & Collaborators

  • American Foundation for Suicide Prevention

    collaborator OTHER
  • Ouida Scholar Award

    collaborator UNKNOWN
  • University of Michigan

    lead OTHER

Principal Investigators

  • Jane Harness, DO · University of Michigan

  • Cheryl King, PhD · University of Michigan

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
24 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-09-17
Primary Completion
2025-10-06
Completion
2025-10-06

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06842667 on ClinicalTrials.gov