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Late Effects and HRQoL in Survivors of Allo-HSCT - a Cross Sectional Study

Rigshospitalet logo

Rigshospitalet

Status

Completed

Conditions

Hematological Diseases

Study type

Observational

Funder types

Other

Identifiers

NCT06277479
Rigshospitalet. Hematology

Details and patient eligibility

About

The cross-sectional study aims to describe the burden of late effects and survivorship-specific health-related quality of life in a nationwide cohort of patients treated with allo-HSCT in Denmark. Further, identify demographic, medical or personal factors associated with better self-reported health and quality of life.

Full description

Objective

The cross-sectional study aims to describe the burden of late effects and survivorship-specific health-related quality of life in a nationwide cohort of patients treated with allo-HSCT in Denmark. Further, identify demographic, medical or personal factors associated with better self-reported health and quality of life.

Method

An observational, descriptive, cross-sectional study using clinical data and self-reported questionnaires to assess the occurrence of comorbidities and self-reported late effects in survivors treated with allo-HSCT in Denmark between 1970 and 2024.

Study population

All survivors treated for malignant or non-malignant hematological disease with allo-HCST at the age of 18-79 years from 1970-2024 in Denmark are eligible (n=1.436).

Endpoints

  • Self-reported survivorship specific HRQoL measured by EORTC-QOL- Survivorship 100.
  • Degree of health literacy measured by the Health Literacy Questionnaire (HLQ).
  • Occurrence or degree of Chronic Graft Versus Host Disease measured by modified Lee Chronic Graft versus host disease Symptom Scale.

Enrollment

1,262 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All survivors treated for malignant or non-malignant hematological disease with allogeneic hematopoietic stem cell transplantation at the age of 18-79 years from 1970-2024 in Denmark are eligible

Exclusion criteria

  • Patient unable to read and understand danish are excluded from study participation

Trial design

1,262 participants in 2 patient groups

AlloHSCT Rigshospitalet
Description:
All patients treated at Department of Hematology, Rigshospitalet
AlloHSCT Skejby
Description:
All patients treated at Department of Hematology, Skejby

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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