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NCT05237986Toboroz

Cognitive Aftereffects of Neurotoxicity in Children and Young Adults With Relapsed/Refractory Hematologic Malignancies Who Receive CAR T-cell Therapy

Investigation of the Cognitive Aftereffects of Neurotoxicity in Children and Young Adults With Relapsed/Refractory Hematologic Malignancies Who Receive CAR T-cell Therapy

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. nov. 3.

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Rövid összefoglaló (regiszter, angolul)

Background: CAR T-cell therapy is a promising new treatment for blood cancers. During treatment, a person s T-cells are genetically changed to kill cancer cells. Researchers want to learn more about the effects of potential problems that may be associated with this treatment. We are specifically interested in learning if and how this treatment may affect the brain or your thinking skills. Objective: To learn if CAR T-cell therapy can affect how children and adults think, process, and remember things. Eligibility: People aged 5-35 who have blood cancer that has not responded to treatment, or the blood cancer has come back after treatment, and who will receive CAR T-cell therapy. Caregivers are also needed. All participants must be able to speak and read in English or Spanish. Design: Participants will be screened with a medical history. Information from participants medical records will be collected. Participants will take tests at home or at NIH to see how well they think, read, learn, remember, reason, and pay attention. The tests will be both computerized and paper/pencil. They will take less than 1 hour to complete. Participants and a parent/adult observer will complete a 5-minute Background Information Form and a checklist of nervous system symptoms. If participants are 5 years or older, they will participate in activities to test their ability to do different thinking tasks, like answer questions, complete puzzle patterns, and remember things. Participants and their caregivers will complete questions to see if they are having specific symptoms related to receiving CAR T-cells. The questions will assess their well-being and needs. The questions will take less than 1 hour to complete. Some tests and questions will be repeated at different time points in the study. Participation will last for up to 3 years....

Állapot (regiszter)
Toboroz
Vizsgálattípus
Megfigyeléses
Résztvevők száma
60 (tervezett)
Első benyújtás
2022. febr. 9.
Kezdés
2025. jún. 23.
Elsődleges befejezés
2028. szept. 1.
Fő szponzor
National Cancer Institute (NCI)
NCT-szám
NCT05237986

Mit vállalsz

  • Vizsgálat típusa: Megfigyeléses
  • Tervezett résztvevők: 60
  • 2025. jún. 23. és az elsődleges befejezés (2028. szept. 1.) között
  • 3 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

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Más betegség

  • -Participants with disease who have a pre-existing global intellectual disability (e.g., Down Syndrome)

A regiszterben nem jelölt feltételek

  • INCLUSION CRITERIA:
  • Participants with disease
    • Participants are diagnosed with relapsed/refractory leukemias or lymphomas, and are scheduled to receive CAR T-cell treatment in one of the enrolling sites
    • For participants enrolled on a CAR T-cell treatment protocol, data sharing for the purposes of this study must be allowed.
    • Age >= 5 and <=35 years old
    • Participant must have an eligible caregiver (informant) who is willing to complete assessments about the participant of this study
    • Participants (<18 years, or >=18 years if needed) must have an eligible caregiver to assist with setting up an appropriate test environment for the remote evaluations
    • Participant must be able to speak and understand English or Spanish
    • Participants must have access to a computer or tablet with a camera and an internet connection
    • Participant or parent/guardian must be able to understand and willing to sign a written consent document
  • Caregivers (informants)
    • Participants must be able to speak and read in English or Spanish
    • Participants who are caregivers for participants with disease addressed above
    • Age >= 18 years old
    • Participants must have access to a computer or tablet
    • Participants (of children <18 years, or >18 years if needed) must be willing to help set up an appropriate test environment for the remote evaluations
    • Participant is able to understand and willing to sign a written consent document

Életkor a regiszterben: 5 év – - · Nem: nők és férfiak · Egészséges önkénteseket is fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (3)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
National Institutes of Health Clinical CenterBethesdaEgyesült ÁllamokToboroz
Children's Hospital of Los AngelesLos AngelesEgyesült ÁllamokToboroz
Seattle Children's HospitalSeattleEgyesült ÁllamokToboroz

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