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RECRUITING NA

Comparing the Stanford Letter Project Form to Traditional Advance Directives

NCT02799537 · View on ClinicalTrials.gov ↗

Study Summary

Our goal is to compare two types of advance directives forms available in English and Spanish to determine which is more easy to use for patients.

Interventions

  • OTHER Randomized clinical study

Study Locations (1)

California

  • Stanford School of Medicine — Stanford

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2016-02
Est. Completion 2026-12
Phase NA

Sponsor

Stanford University

1,643 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02799537

The ClinicalTrials.gov registry entry for NCT02799537 describes a study currently listed as recruiting. 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 1,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stanford University, which has 1,643 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 Palliative Care appearing as the primary indexed condition, and to 1 intervention — of which Randomized clinical study 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: NCT02799537 reports 1 study location spanning 1 distinct geographic area — top geographies include California. 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 NCT02799537 about?

NCT02799537 is a clinical study titled "Comparing the Stanford Letter Project Form to Traditional Advance Directives". Our goal is to compare two types of advance directives forms available in English and Spanish to determine which is more easy to use for patients.

What is the current status of trial NCT02799537?

This trial is currently recruiting. It is a NA study. The enrollment target is 1,000 participants. The study started on 2016-02. Estimated completion is 2026-12.

What conditions does trial NCT02799537 study?

This clinical trial studies the following conditions: Palliative Care, Advance Directives. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02799537?

The interventions under investigation include: Randomized clinical study (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02799537?

This trial is sponsored by Stanford University, which has 1,643 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02799537 being conducted?

This trial has 1 study location across California. 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