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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06842667
Enrollment
506
Registered
2025-02-24
Start date
2025-09-17
Completion date
2025-10-06
Last updated
2025-10-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide Prevention

Brief 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.

Interventions

BEHAVIORALPapageno 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).

BEHAVIORALControl 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

American Foundation for Suicide Prevention
CollaboratorOTHER
Ouida Scholar Award
CollaboratorUNKNOWN
University of Michigan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 24 Years
Healthy volunteers
No

Inclusion criteria

* People who are part of an existing cohort within DesignXM * They will also answer yes to the question: In the past 1 year, have you wished you were dead or wished you could go to sleep and not wake up?

Exclusion criteria

* No exclusions if all inclusion criteria is met

Design outcomes

Primary

MeasureTime frameDescription
Suicidal ideationImmediately before and after watching the video and at 3 monthsAssessed with the Abbreviated Reasons For Living- Young Adult Abbreviated (RFL-YA-II) which consists of 24 questions rated on a scale of 1-6. Higher scores indicate greater importance.
HopelessnessImmediately before and after watching the video and at 3 monthsAssessed with the Beck Hopelessness Scale-4 (BHS-4). The BHS-4 assesses participants' sense of hopelessness, including perceptions of whether their personal actions can improve future outcomes. Participants rate 4 items using a 4 point Likert scale (e.g. My future seems dark to me). Each question is coded 0 for positive expectations and 1 for negative expectations.

Secondary

MeasureTime frameDescription
Participant perceived agencyImmediately before and after watching the video and at 3 monthsAs measured by the Perceived Control Scale which is a single-item measure of participant perceived control. Participants will rate agreement with the statement, right now, I feel like things are out of my control from 0-10 (not at all to a lot).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026