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Mental Stress Symptoms in Family Caregivers of Palliative Patients

Mental Stress Symptoms in Family Caregivers of Palliative Patients

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05054647
Enrollment
100
Registered
2021-09-23
Start date
2021-05-01
Completion date
2024-01-01
Last updated
2023-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Family Caregivers, Palliative Patients

Brief summary

Receiving a life-limiting diagnosis is often a shock for those affected as well as for their relatives, which changes the entire life situation of the family. New perspectives often arise, as well as feelings of worry, sadness and powerlessness. Caregiving is often an extreme physical challenge, but above all a psychological one. Aims of the study 1. To investigate whether family caregivers of palliative patients with severe trait anxiety in the care situation also suffer from severe state anxiety. 2. To investigate whether family caregivers of palliative patients with increased stress levels and burnout-promoting work-related behaviour suffer more from burnout symptoms, health-related anxiety and psychosomatic complaints. 3. To investigate the impact of nursing support by a mobile palliative team on family caregivers of palliative patients.

Interventions

Perceived Stress Scale (PSS-10); Trier-Inventory on Chronic Stress; State/Trait Anxiety Inventory (STAI); AVEM-Work-related behaviour and experience pattern; Maslach Burn-out Inventory - Human Services Survey (MBI - HSS) health-related anxiety: Whiteley Index (WI)

Sponsors

Medical University of Graz
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Women and men between 18 and 90 years of age * Current palliative care situation of a relative with a life-limiting diagnosis.

Exclusion criteria

* Persons incapable of giving consent (e.g. dementia, delirium, etc.) * Failure to meet the inclusion criteria

Design outcomes

Primary

MeasureTime frameDescription
burn-out syndrome, Outcome is the difference between measurement 1 (Baseline) and measurement 2 (Follow-up)2 monthsMaslach Burn-out Inventory (MBI), The MBI does not provide a single score but a profile.

Secondary

MeasureTime frameDescription
health-related anxiety, Outcome is the difference between measurement 1 (Baseline) and measurement 2 (Follow-up)2 monthsWhiteley Index/Illness Attitude Scale (WI-IAS). Whitely-Index: The Whitely-Index is formed by the sum of the points for each answer - the higher the score, the more likely one is to be hypochondriacal. IAS: The total score ranges from 0 to108.
State/Trait anxiety, Outcome is the difference between measurement 1 (Baseline) and measurement 2 (Follow-up)2 monthsState-Trait Anxiety Inventory (STAI). Scores range from 20 to 80, with higher scores correlating with greater anxiety.
Work-related behaviour and experience pattern, Outcome is the difference between measurement 1 (Baseline) and measurement 2.2 monthsWork-related behaviour and experience pattern (AVEM), The AVEM questionnaire does not provide a single score but a profile.

Countries

Austria

Contacts

Primary ContactAndreas Baranyi, MD
an.baranyi@medunigraz.at004331638586241

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026