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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05044845
Other study ID # BINFORMED
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 18, 2022
Est. completion date January 2025

Study information

Verified date February 2024
Source St. Jude Children's Research Hospital
Contact Nidhi Bhatt, MD
Phone 901-426-6982
Email binformedstudy@stjude.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Gene therapy is a paradigm-shifting treatment for hemophilia B patients, particularly in resource-limited countries where factor availability remains low. Transparent and culturally sensitive communication around gene therapy is vital to the success of a high-quality consenting process. Current literature on knowledge, beliefs and attitudes about gene therapy in resource-limited countries is inadequate. In addition, few educational resources to explain basic gene therapy concepts exist in languages other than English. This study aims to address these gaps in knowledge and aid for the development of educational resources to assist the informed consent processes for gene therapy in resource-limited countries. Primary Objective: To assess baseline knowledge, beliefs, and attitudes about gene therapy held by hemophilia B patients globally Secondary Objectives: 1. To explore healthcare workers' (i.e., physicians, nurses, social workers, educators/academic coordinators) perspectives regarding the education needs of hemophilia B patients globally 2. To explore healthcare workers beliefs and attitudes about gene therapy 3. To identify preferences of patients with hemophilia B and their healthcare workers on how/by what method or pathway educational content should be provided.


Description:

This prospective cohort study will use qualitative methods, specifically semi structured interviews to evaluate knowledge, beliefs, and attitude about gene therapy in patients 12 years and older with a diagnosis of moderate and severe hemophilia B (≤2% FIX activity only), caregivers/parents and healthcare workers who care for them at St. Jude and other global countries. Participants will be interviewed virtually using an online video-conferencing platform, phone or in person. Interviews will be performed by experienced qualitative interviewers in the official language of each participating site. Interviews will last approximately 45-60 minutes and will be performed only once. All interviews will be audio recorded and obtained information will be analyzed using semantic content analysis to identify common themes.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date January 2025
Est. primary completion date December 2024
Accepts healthy volunteers
Gender All
Age group 12 Years and older
Eligibility Inclusion Criteria: - Patients =12 years of age - Diagnosis of moderate (FIX =1% and =2%) or severe (<1%) hemophilia B - Parents or caregivers to patients with hemophilia 12-17 years of age Inclusion Criteria - Healthcare worker: - Doctors, nurses, social workers, pharmacists and educators who participate in the care of hemophilia B patients Exclusion Criteria: - Diagnosis of Hemophilia A - Diagnosis of other non-Hemophilia B bleeding disorders Exclusion Criteria - Healthcare worker: - Health care workers who do not participate in the care of hemophilia B patients - Healthcare worker who is conducting the interviews

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Interview
Semi structured interview will be conducted virtually using an online video-conferencing platform, phone or in person.

Locations

Country Name City State
United States St. Jude Children's Research Hospital Memphis Tennessee

Sponsors (1)

Lead Sponsor Collaborator
St. Jude Children's Research Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Use of semi-structured interviews to qualitatively describe their attitudes, beliefs, and knowledge of gene therapy in hemophilia B Semi-structured interviews will be performed in patients with hemophilia B, their caregivers and healthcare workers to qualitatively describe their attitudes, beliefs, and knowledge of gene therapy in hemophilia B including concerns, expectations, and best way to receive information about gene therapy. Interviews will be audio recorded, transcribed verbatim and analyzed using semantic content analysis to identify common themes. Day 1, or at a future visit (up to approximately 1 year)
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