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NCT05126810 · ClinicalTrials.gov registry record

Willingness to Participate in a Trial Comparing Standard Genetic Counseling Versus Personalized Genetic Counseling

A clinical trial of Li-Fraumeni Syndrome, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
500
Enrollment target
1
Study location

NCT05126810: Recruiting study of Li-Fraumeni Syndrome, sponsored by M.D. Anderson Cancer Center.

NCT05126810 is a study of Li-Fraumeni Syndrome that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 500 participants, below the 1,993-participant average among 6 other Li-Fraumeni Syndrome trials with a reported enrollment target (75% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05126810, a study of Li-Fraumeni Syndrome, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

RECRUITING
Registry status
500 participants
Enrollment target
1
Study location

Study Summary

This study evaluates patients willingness to participate in a trial comparing standard genetic counseling versus personalized genetic counseling. Collecting information from patients may help researchers learn why patients may or may not take part in the future study that compares standard genetic counseling to personalized genetic counseling.

Conditions Studied

Interventions

  • OTHER Questionnaire Administration

Study Locations (1)

Texas

  • M D Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2022-11-03
Est. Completion 2027-10-02
M.D. Anderson Cancer Center

2,692 total trials

What NCT05126810 shows while recruiting

NCT05126810 is an observational study that tracks outcomes without assigning an intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap, below the 1,993-participant average among 6 other Li-Fraumeni Syndrome trials with a reported enrollment target (75% lower).

The record links to 1 condition, with Li-Fraumeni Syndrome appearing as the primary indexed condition, and to 1 intervention - of which Questionnaire Administration is the first listed.

NCT05126810 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT05126810 about?

NCT05126810 is a clinical study titled "Willingness to Participate in a Trial Comparing Standard Genetic Counseling Versus Personalized Genetic Counseling". This study evaluates patients willingness to participate in a trial comparing standard genetic counseling versus personalized genetic counseling. Collecting information from patients may help researchers learn why patients may or may not take part in the future study that compares standard genetic c...

What is the current status of trial NCT05126810?

This trial is currently recruiting. The enrollment target is 500 participants. The study started on 2022-11-03. Estimated completion is 2027-10-02.

What conditions does trial NCT05126810 study?

This clinical trial studies the following conditions: Li-Fraumeni Syndrome.

What interventions are being tested in trial NCT05126810?

The interventions under investigation include: Questionnaire Administration (OTHER).

Who is sponsoring clinical trial NCT05126810?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05126810 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT05126810, the US trial registry maintained by the National Library of Medicine. NCT05126810 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.