Understanding quality of life and stress in stroke patients and their caregivers

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to investigate the quality of life, stress levels, and caregiver burden in stroke patients and their caregivers. Participants will complete questionnaires and provide hair samples to measure stress hormones, alongside consenting to the use of their clinical and laboratory data. The study will compare these participants to a control group without stroke to establish a baseline for quality of life and stress factors. The research will be conducted over 12 months, with sequential measurements to uncover relationships between patient impairments and the quality of life of both patients and caregivers.

Why it matters

Who can join: the full rules

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

Where it's running

• Department of Neurology, University Hospital Zurich
  Zurich, Canton of Zurich, Switzerland Recruiting

Study contacts

• Principal investigator: Susanne Wegener, MD — University of Zurich
• Study coordinator: Anton Schmick, MD
• Email: anton.schmick@usz.ch
• Phone: +41442551111

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Observational study of patients with spontaneous intracerebral hemorrhage

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• Evaluating the impact of artery calcification on stroke treatment outcomes

  This study is trying to see if the amount of calcium in the arteries affects how well stroke patients do after a specific treatment for blocked blood vessels.

  Recruiting Zhujiang Hospital · Guangzhou, Guangdong · NCT06418698

How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.