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NCT06227962Enrolling by invitation

Cognitive Functioning and Health Related Quality of Life in Retinoblastoma Survivors

Cognitive Functioning and Health Related Quality of Life in Retinoblastoma Survivors (8-35 Years): The Role of Cancer Treatment and Repeated Anesthesia

Source: ClinicalTrials.gov · Last updated 4 Dec 2025

Brief summary (registry, in English)

A retrospective crosssectional observational study of the effects of oncological treatment and frequent general anesthesia on neuropsychological development, psychosocial functioning (in terms of anxiety, depression, peer relations, perceived cognitive functioning and potential trauma) and health related quality of life in children and young adults who were treated or screened for retinoblastoma.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
240 (estimated)
First submitted
20 Dec 2023
Start date
26 Oct 2023
Primary completion date
30 Oct 2026
Lead sponsor
Amsterdam University Medical Center
NCT number
NCT06227962

What you commit to

  • Study type: Observational
  • Planned participants: 240
  • From 26 Oct 2023 to the primary completion date, 30 Oct 2026
  • 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

  • Rb diagnostic trajectory, treatment and follow-up at another hospital or before the founding of the Dutch Retinoblastoma Expertise Center in 1991. With exception of Rb survivors (diagnosed \>1991) who apart from treatment at the Dutch Retinoblastoma Center also required specialized treatment (such as radiation) at another center: they are illegible for inclusion.

Other illness

  • Having an active, uncontrolled psychiatric illness,

Other

  • Pre-existing documented developmental delay and/or severe cognitive impairments (IQ \<70),

Who the study is looking for

  • Rb diagnosis, (main) treatment and follow-up of Rb patients and -survivors, or Rb screening took place at the Dutch Retinoblastoma Expertise Center of the Amsterdam University Medical Center,
  • Rb survivor or former Rb risk carriers is between 8 and 35 years old,
  • Average understanding of the Dutch language.
  • Being a caregiver of a Rb survivor or Rb risk carrier that have been diagnosed and receive(d) (main) treatment and follow-up or screening at the Dutch Retinoblastoma Expertise Center of the Amsterdam University Medical Center,
  • The related Rb survivor or Rb risk carrier is \< 12 years old,
  • Average understanding of the Dutch language.

Age in the registry: 6 months to 35 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Amsterdam University Medical Center
Coordinator of this site? Confirm its status
AmsterdamNetherlandsUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.