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COMPLETED NA

Cognitive Behavioral Therapy for Insomnia vs. Exposure, Relaxation, and Rescripting Therapy

NCT03831412 · View on ClinicalTrials.gov ↗

Study Summary

The objective of this project is to determine if directly addressing disturbed sleep and nightmares will impact client reports of suicidal ideation.

Interventions

  • BEHAVIORAL CBT-I
  • BEHAVIORAL ERRT

Study Locations (1)

Oklahoma

  • Lorton Hall — Tulsa

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2017-08-01
Est. Completion 2021-01-31
Phase NA

Sponsor

University of Tul

33 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03831412

The ClinicalTrials.gov registry entry for NCT03831412 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 13 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Tul, which has 33 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Insomnia appearing as the primary indexed condition, and to 2 interventions — of which CBT-I 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: NCT03831412 reports 1 study location spanning 1 distinct geographic area — top geographies include Oklahoma. 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 NCT03831412 about?

NCT03831412 is a clinical study titled "Cognitive Behavioral Therapy for Insomnia vs. Exposure, Relaxation, and Rescripting Therapy". The objective of this project is to determine if directly addressing disturbed sleep and nightmares will impact client reports of suicidal ideation.

What is the current status of trial NCT03831412?

This trial is currently completed. It is a NA study. The enrollment target is 13 participants. The study started on 2017-08-01. Estimated completion is 2021-01-31.

What conditions does trial NCT03831412 study?

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

What interventions are being tested in trial NCT03831412?

The interventions under investigation include: CBT-I (BEHAVIORAL), ERRT (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03831412?

This trial is sponsored by University of Tul, which has 33 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03831412 being conducted?

This trial has 1 study location across Oklahoma. 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