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

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 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.

View on ClinicalTrials.gov ↗

View your shortlist →

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

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT05126810

The ClinicalTrials.gov registry entry for NCT05126810 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,993-participant average among 6 other Li-Fraumeni Syndrome trials with a reported enrollment target (75% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

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 1 study location spanning 1 distinct geographic area - top geographies include 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.

Similar trials for Li-Fraumeni Syndrome

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.