Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID05867706

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

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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)

Long-term Monitoring

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

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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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