Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED NA

Reconnecting: Improving Interoception to Reduce Suicidal Ideation in the Military

NCT04103385 · View on ClinicalTrials.gov ↗

Study Summary

Background: Interoception is defined as the "sense of the physiological condition of the entire body" and is crucial for recognizing emotions and sensations (e.g., hunger, temperature, pain) and responding accordingly. The investigator's lab has conducted several independent studies and two pilot studies that support the hypothesis that disrupted interoception leads one to be disconnected from the body, and thus more able to harm the body should one desire to do so. Research suggests that interoceptive deficits may not only differentiate those who are thinking about suicide from those who engage in suicidal behavior, but it may also provide information about who is at imminent risk for suicidal behavior. The identification of novel, short-term risk factors, like interoceptive deficits, allows for the development of new treatment applications for suicide, which is important for several reasons: 1) suicide rates have increased in recent years, especially among military populations, and 2) existing treatment approaches are often ineffective, lengthy, expensive, or impractical for large-scale dissemination. This project evaluates a novel, brief intervention for interoceptive deficits and suicidal behavior with the potential to be acceptable and feasible for a military population.

Interventions

  • BEHAVIORAL RISE (Reconnecting to Internal Sensations and Experiences)
  • BEHAVIORAL RISE (Reconnecting to Individual Strength and Energy)

Study Locations (2)

Ohio

  • Wright Patterson Medical Center — Dayton

Washington

  • Madigan Army Medical Center — Tacoma

Trial Details

FieldValue
Enrollment Target 195 participants
Start Date 2020-06-01
Est. Completion 2021-11-22
Phase NA

Sponsor

Miami University

2 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04103385

The ClinicalTrials.gov registry entry for NCT04103385 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 195 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Miami University, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Suicidal Ideation appearing as the primary indexed condition, and to 2 interventions — of which RISE (Reconnecting to Internal Sensations and Experiences) 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: NCT04103385 reports 2 study locations spanning 2 distinct geographic areas — top geographies include Ohio, Washington. 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 NCT04103385 about?

NCT04103385 is a clinical study titled "Reconnecting: Improving Interoception to Reduce Suicidal Ideation in the Military". Background: Interoception is defined as the "sense of the physiological condition of the entire body" and is crucial for recognizing emotions and sensations (e.g., hunger, temperature, pain) and responding accordingly. The investigator's lab has conducted several independent studies and two pilot st...

What is the current status of trial NCT04103385?

This trial is currently completed. It is a NA study. The enrollment target is 195 participants. The study started on 2020-06-01. Estimated completion is 2021-11-22.

What conditions does trial NCT04103385 study?

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

What interventions are being tested in trial NCT04103385?

The interventions under investigation include: RISE (Reconnecting to Internal Sensations and Experiences) (BEHAVIORAL), RISE (Reconnecting to Individual Strength and Energy) (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04103385?

This trial is sponsored by Miami University, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT04103385 being conducted?

This trial has 2 study locations across Ohio, Washington. 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