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COMPLETED NA

Promoting Safety Plan and Coping Strategy Use Among Adults With Suicidal Thoughts

NCT05791643 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this study is to learn about a new, real-time, smartphone-based intervention aimed to decrease risk for suicide in adults who have been hospitalized for suicidal thoughts or behaviors. The main questions the investigators aim to answer are: * Is a real-time, smartphone-based intervention that promotes the use of safety plans and other coping strategies for suicidal thoughts feasible and acceptable? * Does the real-time intervention result in increased use of safety plans and other coping strategies, and reduce suicidal thoughts? Participants will: * Answer questions about current suicidal thoughts on their smartphone up to 6 times each day while they are in the hospital and during the 4 weeks after they leave the hospital * When they report elevated suicidal thoughts on a smartphone survey, be randomly assigned to receive or not receive automated, interactive reminders to use content from their personalized safety plan or general coping strategies * Answer brief follow-up questions on their smartphone within a couple hours of receiving or not receiving automated reminders * Give feedback on their experience with the real-time intervention

Conditions Studied

Interventions

  • BEHAVIORAL Personalized internal and external coping strategies
  • BEHAVIORAL Personalized internal coping strategies
  • BEHAVIORAL Personalized external coping strategies
  • BEHAVIORAL General internal and external coping strategies
  • BEHAVIORAL General internal coping strategies

Study Locations (2)

Massachusetts

  • McLean Hospital — Belmont
  • Massachusetts General Hospital — Boston

Trial Details

FieldValue
Enrollment Target 103 participants
Start Date 2023-07-05
Est. Completion 2024-09-03
Phase NA

Sponsor

Massachusetts General Hospital

1,948 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05791643

The ClinicalTrials.gov registry entry for NCT05791643 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 103 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Massachusetts General Hospital, which has 1,948 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Suicide appearing as the primary indexed condition, and to 5 interventions — of which Personalized internal and external coping strategies is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT05791643 reports 2 study locations spanning 1 distinct geographic area — top geographies include Massachusetts. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT05791643 about?

NCT05791643 is a clinical study titled "Promoting Safety Plan and Coping Strategy Use Among Adults With Suicidal Thoughts". The goal of this study is to learn about a new, real-time, smartphone-based intervention aimed to decrease risk for suicide in adults who have been hospitalized for suicidal thoughts or behaviors. The main questions the investigators aim to answer are: * Is a real-time, smartphone-based interventio...

What is the current status of trial NCT05791643?

This trial is currently completed. It is a NA study. The enrollment target is 103 participants. The study started on 2023-07-05. Estimated completion is 2024-09-03.

What conditions does trial NCT05791643 study?

This clinical trial studies the following conditions: Suicide. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05791643?

The interventions under investigation include: Personalized internal and external coping strategies (BEHAVIORAL), Personalized internal coping strategies (BEHAVIORAL), Personalized external coping strategies (BEHAVIORAL), General internal and external coping strategies (BEHAVIORAL), General internal coping strategies (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05791643?

This trial is sponsored by Massachusetts General Hospital, which has 1,948 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05791643 being conducted?

This trial has 2 study locations across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial