NCT05810181Recruiting
Gene Therapy Communication: Use of a Needs Assessment to Drive Decision-AIDS for Gene Therapy for Rare Diseases (GENETX)
Source: ClinicalTrials.gov · Last updated 10 Aug 2026
Brief summary (registry, in English)
This prospective mixed-method interview study aims to qualitatively describe the beliefs, attitudes, and informational needs around gene therapy for rare pediatric diseases among patients and parents of children with a rare disease targeted for treatment using gene therapy techniques. Using learned insights, the team will develop an online platform providing educational content and patient decision aids for patients and their families.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 145 (estimated)
- First submitted
- 30 Mar 2023
- Start date
- 1 Jun 2023
- Primary completion date
- Dec 2027
- Lead sponsor
- St. Jude Children's Research Hospital
- Diseases
- Sickle cell disease
- NCT number
- NCT05810181
What you commit to
- Study type: Observational
- Planned participants: 145
- From 1 Jun 2023 to the primary completion date, Dec 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Condition or chronic illness, which in the opinion of the PI/Co-I, makes participation unsafe or untenable (i.e., cognitive impairment, concurrent acute morbidity).
Other
- Participants who are unable to converse fluently in English will be excluded.
- Inability or unwillingness of research participant to give verbal informed consent.
- Participants who lack access to a computer or mobile device that supports video communications will be excluded.
Who the study is looking for
- For Group 1 participants only (Undergone Gene Therapy):
- Parent/caregiver whose child has undergone gene therapy. OR Parent/caregiver of a child who died after receiving gene therapy at least 6 months prior to enrollment, but no more than 24 months prior to enrollment, to be contacted no sooner than 3 months after the death has occurred and no longer than 2 years. OR Patients age 8 and above who have undergone gene therapy.
- Willingness to participate in one-on-one video interview with a study team member using a personal mobile device or computer with working internet connection.
- Must be willing to provide verbal informed consent.
- Release of information form signed by participant providing our study team with permission to contact healthcare provider to verify their diagnosis and receipt of gene therapy (if received).
- Successful verification of diagnosis of rare genetic disease targeted for treatment using gene therapy.
- A positive confirmation on receipt of gene therapy and type received from their healthcare provider (only for those received gene therapy).
- For Group 2 participants only (Offered, but did not Undergo Gene Therapy):
- Parent/caregiver of children (or patients 8 and above ) with a rare genetic disease who had been offered but were not eligible for a trial or decided against receiving gene therapy.
- Willingness to participate in one-on-one video interview with a study team member using a personal mobile device or computer with working internet connection.
- Must be willing to provide verbal informed consent.
- Signed release of information form providing GeneTx study team with permission to contact participant's healthcare provider to verify the diagnosis.
- Successful verification of diagnosis of rare genetic disease targeted for treatment using gene therapy.
- For Group 3 participants only (Provider Interviews):
- Healthcare worker who has provided care to ≥ 2 patients receiving gene therapy.
- Willingness to participate in one-on-one video (or in-person) interview with a study team member using a personal mobile device or computer with working internet connection.
- Informed consent from a study participant.
- For Group 4 participants only (Undergone Gene Therapy for Bone Marrow Failure Condition):
- Parent/caregiver whose child has undergone gene therapy. OR Parent/caregiver of a child who died after receiving gene therapy at least 6 months prior to enrollment, but no more than 24 months prior to enrollment, to be contacted no sooner than 3 months after the death has occurred and no longer than 2 years. OR Patients age 8 and above who have undergone gene therapy.
- Willingness to participate in one-on-one video interview with a study team member using a personal mobile device or computer with working internet connection.
- Must be willing to provide verbal informed consent.
- Release of information form signed by participant providing our study team with permission to contact healthcare provider to verify their diagnosis and receipt of gene therapy (if received).
- Successful verification of diagnosis of rare genetic disease targeted for treatment using gene therapy.
- A positive confirmation on receipt of gene therapy and type received from their healthcare provider (only for those received gene therapy).
- For Group 5 participants only (Offered, but did not Undergo Gene Therapy for Bone Marrow Failure Condition ):
- Parent/caregiver of children (or patients 8 and above ) with a bone marrow failure disease who had been offered but were not eligible for a trial or decided against receiving gene therapy.
- Willingness to participate in one-on-one video interview with a study team member using a personal mobile device or computer with working internet connection.
- Must be willing to provide verbal informed consent.
- Signed release of information form providing GeneTx study team with permission to contact participant's healthcare provider to verify the diagnosis.
- Successful verification of diagnosis of rare genetic disease targeted for treatment using gene therapy.
- For Group 6 participants only (Never offered gene therapy for Bone Marrow Failure Condition):
- Parent/caregiver of children (or patients 8 and above ) with a bone marrow failure disease who had not been offered gene therapy.
- Willingness to participate in one-on-one video interview with a study team member using a personal mobile device or computer with working internet connection.
- Must be willing to provide verbal informed consent.
- Signed release of information form providing GeneTx study team with permission to contact participant's healthcare provider to verify the diagnosis.
- Successful verification of diagnosis of rare genetic disease targeted for treatment using gene therapy.
- For Group 7 participants only (Provider Interviews for Bone Marrow Failure Condition):
- Healthcare worker who has provided care to ≥ 2 patients receiving gene therapy.
- Willingness to participate in one-on-one video (or in-person) interview with a study team member using a personal mobile device or computer with working internet connection.
- Informed consent from a study participant.
Age in the registry: 8 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| St. Jude Children's Research Hospital Coordinator of this site? Confirm its status | Memphis | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.