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Search / Trial NCT06443268

Cerebrovascular Disease: Quality of Life (CODE: QoL)

Launched by UNIVERSITY OF ZURICH · May 29, 2024

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

Stroke, Qo L, Hr Qo L, Patient Caregiver Dyads, Stress, Burden

ClinConnect Summary

The CODE: QoL study is looking to understand how strokes and other cerebrovascular conditions affect the quality of life for both patients and their caregivers. Researchers want to explore the levels of stress experienced by these individuals and what factors might contribute to their overall well-being. Patients who have had a stroke, as well as their caregivers, will be asked to fill out questionnaires and provide a hair sample to measure stress hormones. There will also be a comparison group of individuals who have not experienced a stroke, which will help researchers understand how these conditions impact quality of life.

To participate, patients must be over 18 years old and have recently experienced a stroke or a related condition, while caregivers must also be 18 or older. Both the patients and their caregivers need to be able to give their consent to join the study. Participants will be involved in answering questions and providing samples, helping to shed light on the challenges faced by those living with the effects of a stroke. This study is currently recruiting participants at the University Hospital of Zurich and aims to provide valuable insights into the well-being of patients and their caregivers.

Gender

ALL

Eligibility criteria

  • Control group:
  • Inclusion criteria:
  • over 18 years old
  • No previous stroke OR previous stroke \>3 years ago
  • No significant disability (maximum mRS 1)
  • ambulatory patients at the University Hospital of Zurich (USZ), Dept. of Neurology
  • Patients' AND caregiver's ability to give informed consent
  • Patients' AND close relative's / caregiver's willingness to participate
  • Exclusion criteria:
  • • Medication with steroid hormones (prednisone, prednisolone, dexamethasone, methylprednisolone, hydrocortisone etc.) within last 3 months
  • Main Group:
  • Inclusion criteria:
  • over 18 years old
  • Patients diagnosed with either transient ischemic attack, ischemic stroke or intracerebral hemorrhage and their caregivers
  • Caregiver of a patient as described above, age over 18 years
  • Hospitalized or ambulatory patients at the University Hospital of Zurich (USZ) included within 28 days from event.
  • Patients' AND caregiver's ability to give informed consent
  • Patients' AND caregiver's willingness to participate
  • Exclusion criteria:
  • • Medication with steroid hormones (prednisone, prednisolone, dexamethasone, methylprednisolone, hydrocortisone etc.) within last 3 months

About University Of Zurich

The University of Zurich, a leading institution in research and education, is dedicated to advancing medical knowledge and improving patient care through innovative clinical trials. With a robust framework for conducting high-quality research, the university collaborates with multidisciplinary teams of experts to explore cutting-edge therapeutic approaches and interventions. Its commitment to ethical standards and patient safety ensures that all clinical trials are conducted with the utmost integrity, aiming to contribute valuable insights to the medical community and enhance health outcomes globally.

Locations

Zürich, Zurich, Switzerland

Patients applied

0 patients applied

Trial Officials

Susanne Wegener, MD

Principal Investigator

University of Zurich

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported