Actively Recruiting
The Psychobiological Adjustment to Bereavement Among Cancer Caregivers
Led by University of Zurich · Updated on 2025-04-04
150
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Zurich
Lead Sponsor
U
University of Salzburg
Collaborating Sponsor
AI-Summary
What this Trial Is About
The loss of a spouse, especially after caring for a terminally ill partner, is a highly stressful event linked to increased risk of mental and physical health problems. This research investigates how individual differences in psychological factors like depression and grief, along with biological markers such as inflammation and cortisol levels, influence short- and long-term adjustment to bereavement. The study seeks to understand why some people develop prolonged grief or health issues while others show resilience. Participants are caregivers or spouses of patients with terminal illnesses expected to live six months or less. The study observes these individuals over time, assessing psychological and biological markers before and after the patient's death. Measurements occur at three points: six months before the patient's death, 3-6 months post-loss, and 9-12 months post-loss. Data collected include depression scales, inflammatory markers, stress inventories, sleep quality, heart rate variability, and other health questionnaires. During the study, participants complete various questionnaires and provide biological samples at each assessment point. Researchers track psychological symptoms, stress levels, immune and endocrine function, and physical health to identify patterns of adjustment to loss. The study aims to reveal factors influencing resilience or vulnerability after bereavement, helping to guide future treatments to support health outcomes in grieving spouses. Participation spans from before the patient's death through one year after the loss, with multiple evaluations along the way.
CONDITIONS
Brief Title
Caregiver Stress and Bereavement
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant age 218 years or older
- Caregiver or spouse of a patient with a terminal illness expected to live 6 months or less
- Primary caregiver involved intimately in the patient's care since diagnosis
- German is the participant's primary language
- Signed informed consent is provided
You will not qualify if you...
- Significant visual or hearing problems or cognitive impairment
- Morbid obesity with body mass index 40 kg/m2 or higher
- Alcohol or drug abuse
- Active cancer diagnosis
- Severe illnesses such as respiratory, heart, liver, or kidney failure
- Major immune system conditions including diabetes, autoimmune diseases, asthma, or thyroid disorders
- Severe high blood pressure over 200/120 mmHg
- Regular use of medications affecting the immune system like corticosteroids or immunosuppressants
- Pregnant or breastfeeding
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 6 months before patient's death
Participants undergo assessments to evaluate psychological and biological markers before the loss of their spouse.
1 visit (in-person)
Duration - From 3 to 12 months post-loss
Participants are monitored for psychological and biological changes following the loss of their spouse to understand adjustment to bereavement over time.
2 visits (in-person) at 3-6 months and 9-12 months post-loss
Trial Site Locations
Total: 1 location
1
University Hospital Zurich
Zurich, Canton of Zurich, Switzerland, 8091
Actively Recruiting
Research Team
A
Annina Seiler, PD PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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