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NCT05064241 · ClinicalTrials.gov registry record · NA

Overcoming Barriers to Accessing Genetic Medicine

A NA study of Genetic Disease and Genetic Predisposition, sponsored by Boston Children's Hospital.

Active
Registry status
NA
Development phase
70
Enrollment target
1
Study location

NCT05064241 is a NA study of Genetic Disease and Genetic Predisposition that is active but no longer recruiting, run by Boston Children's Hospital. The registered enrollment target is 70 participants, below the 2,559-participant average among 30 other Genetic Disease trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05064241, a NA study of Genetic Disease and Genetic Predisposition, is active but no longer recruiting, sponsored by Boston Children's Hospital.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
70 participants
Enrollment target
1
Study location

Study Summary

To learn about patient barriers to accessing genetic medicine, we will analyze anonymous posts from a membership-based online community \[Inspire.com\], and investigate how these barriers differ for various populations. We will then test whether these barriers can be addressed by providing online access to a genetic counselor to answer patient questions for one group of patients (virtual advisory board group) and compare to that of a control group who does not have access to a genetic counselor (virtual peer-to-peer board group).

Interventions

  • OTHER Access to Genetic Counselor for answering questions

Study Locations (1)

Massachusetts

  • Boston Children's Hospital - Boston

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2023-04-15
Est. Completion 2025-09-30
Phase NA

Sponsor

Boston Children's Hospital

462 total trials

What the Registry Record Tells You About NCT05064241

The ClinicalTrials.gov registry entry for NCT05064241 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,559-participant average among 30 other Genetic Disease trials with a reported enrollment target (97% lower). The listed sponsor is Boston Children's Hospital, which has 462 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Genetic Disease appearing as the primary indexed condition, and to 1 intervention - of which Access to Genetic Counselor for answering questions is the first listed.

NCT05064241 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT05064241 about?

NCT05064241 is a clinical study titled "Overcoming Barriers to Accessing Genetic Medicine". To learn about patient barriers to accessing genetic medicine, we will analyze anonymous posts from a membership-based online community \[Inspire.com\], and investigate how these barriers differ for various populations. We will then test whether these barriers can be addressed by providing online ac...

What is the current status of trial NCT05064241?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 70 participants. The study started on 2023-04-15. Estimated completion is 2025-09-30.

What conditions does trial NCT05064241 study?

This clinical trial studies the following conditions: Genetic Disease, Genetic Predisposition.

What interventions are being tested in trial NCT05064241?

The interventions under investigation include: Access to Genetic Counselor for answering questions (OTHER).

Who is sponsoring clinical trial NCT05064241?

This trial is sponsored by Boston Children's Hospital, which has 462 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05064241 being conducted?

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

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

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