CClinicalTrials.gg
Enrolling by invitationNCT07314801FINCARE-YoungUpdated Jan 2, 2026

FINancial Toxicity and CAncer REcovery in YOUNG Adults

An observational study in Financial Toxicity Related to Cancer Diagnosis and Tretment in Adolescents and Young Adults, sponsored by University Medical Center Goettingen. Enrolling by invitation at 1 site in Germany. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2026-01-02.

Sponsored by University Medical Center Goettingen · Observational

From the registry’s dates

  • Primary completion was expected by Apr 2026, 6 months ago, but the record still lists the study as enrolling by invitation.
Study type
Observational
Model
Cohort
Time perspective
Cross-sectional
Enrollment
300
Ages
18 Years to 50 Years
Sex
All
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Study summary

The FINCARE-Young study aims to investigate the extent and development of financial toxicity in adolescents and young adults with cancer. The primary purpose of this study is to assess the level of financial burden experienced during the acute phase of cancer treatment and after completion of therapy, and to analyze changes over time. In addition, the study seeks to identify sociodemographic, clinical, and socioeconomic factors associated with financial toxicity, as well as its impact on employment and social reintegration. By focusing on young adult cancer survivors, this study addresses an underexplored population and seeks to generate evidence to improve supportive care strategies and reduce long-term financial consequences of cancer.

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Conditions studied

  • Financial Toxicity Related to Cancer Diagnosis and Tretment in Adolescents and Young Adults
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In context

Lead sponsor

University Medical Center Goettingen is the lead sponsor of 61 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population will be selected from adolescents and young adults with a history of cancer who were treated at the University Medical Center Göttingen, a tertiary care academic hospital in Germany. Potential participants are identified through institutional clinical databases and electronic medical records. The source population includes individuals who received oncological care across all cancer entities within this center over the defined study period and who can be contacted for follow-up after completion of therapy.

Inclusion criteria

  • Age 18 to 39 years at the time of initial cancer diagnosis
  • Diagnosis of a malignant neoplasm
  • Receipt of oncological treatment at the University Medical Center Göttingen
  • Completion of primary cancer therapy at the time of study participation
  • Initial diagnosis between 2014 and 2024
  • Ability to provide informed consent
  • Sufficient German language skills to participate in a telephone interview and complete questionnaires

Exclusion criteria

Exclusion Criteria:

  • Age below 18 years or above 39 years at the time of initial cancer diagnosis
  • No history of malignant disease
  • Ongoing primary cancer treatment at the time of study participation
  • Severe cognitive impairment or psychiatric condition preventing reliable participation
  • Insufficient German language proficiency to complete interviews or questionnaires
  • Withdrawal of informed consent
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Study design

Observational model
Cohort
Time perspective
Cross-sectional
Enrollment
300 participants (estimated)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • Adolescents and Young Adults with Cancer

    This cohort consists of adolescents and young adults aged 18 to 39 years at the time of initial cancer diagnosis who received oncological treatment at a single tertiary care center. Participants have completed their primary cancer therapy and are assessed retrospectively and prospectively. The study does not involve any therapeutic intervention. Data are collected through structured telephone interviews and standardized questionnaires, complemented by clinical data extracted from electronic medical records. The focus of the cohort is to evaluate financial toxicity, socioeconomic factors, and employment-related outcomes following cancer treatment.

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What researchers measure

Primary outcomes

  1. Financial toxicity

    Financial toxicity, assessed using the Comprehensive Score for Financial Toxicity (COST) questionnaire, measured during the acute phase of cancer treatment and at the time of study participation, including change over time.

    Time frame: From the acute phase of cancer treatment to the time of study participation after completion of therapy (retrospective assessment of treatment period and current assessment at follow-up), assessed only at one time point at study enrollment.

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Study locations

1 site
  • University Medicine Göttingen
    Göttingen, Lower Saxony 37075, Germany
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References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared because the study involves highly sensitive personal, medical, and socioeconomic information. Sharing individual-level data could pose a risk to participant privacy and confidentiality, even after pseudonymization, and is therefore not planned.

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07314801
Lead sponsor
University Medical Center Goettingen
Responsible party
Prof. Dr. Rami El Shafie (Prof. Dr., University Medical Center Goettingen) — Principal investigator
First posted
Jan 2, 2026
Start date
Dec 2025 (estimated)
Primary completion
Apr 2026 (estimated)
Completion
Apr 2026 (estimated)
Last update
Jan 2, 2026

Study contacts

Rami El Shafie, Prof. Dr.
principal investigator · University Medicine Göttingen

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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No contact was published for this record. The registry link below has the sponsor’s details.

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