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Collateral Effects of Pandemics - Care for Informal Caregivers

Collateral Effects of Pandemics - Care for Informal Caregivers

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06302283
Acronym
COLLPAN-3A
Enrollment
400
Registered
2024-03-08
Start date
2024-03-31
Completion date
2024-12-31
Last updated
2024-03-08

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

Conditions

Bereavement

Keywords

Informal Caregiver burden

Brief summary

The study is a workpackage in the German research consortium COLLPAN. The study will map collateral effects in terms of psychosocial and spiritual burden of informal caregivers during after the pandemic and identification/mapping of risk factors.It will also map available therapeutic and preventive interventions and relief of this burden for the present situation and for future pandemics.

Detailed description

a scoping literature review will compile evidence on informal caregiver burden during and after the pandemic (PubMed, PsychInfo, Cochrane Database). The aim of the review is to gain knowledge on frequency, severity, source and circumstances of care givers' burden and to identify research and supportive gaps. The study will recruit family members and care givers of patients with COVID-19 or long-COVID as well as bereaved family members and care givers of patients who have died during the pandemic in order to assess severity of burden. Recruitment will be done in collaboration with the German Association of Undertakers and the Federal Association for Bereavement Care. Family members and caregivers will be asked to complete a survey with instruments on bereavement burden (PG- 13), distress (PHQ-9; GAD-7) and care giver symptoms (IPOS; MIDOS-2). The survey will be available online (using SoSciSurvey platform) or as a paper and pencil version. Survey participants will be invited to in-depth interviews. Recruitment of 200 participants each for caregiving of COVID-19 patients and bereaved family members will be targeted. Interviews are planned with 30 participants in each group or until saturation is reached. Based on findings, recommendations on interventions to support family care givers will be developed

Interventions

OTHERSurvey

Survey (online or paper) on caregiving burden and bereavement

Sponsors

Wuerzburg University Hospital
CollaboratorOTHER
Johannes Gutenberg University Mainz
CollaboratorOTHER
Universitätsklinikum Hamburg-Eppendorf
CollaboratorOTHER
University of Bonn
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* having cared for a patient with COVID-19 in the first year of the pandemic (March to December 2021)

Exclusion criteria

* not fluent in German

Design outcomes

Primary

MeasureTime frameDescription
Bereavement burdenBaselinestandardized instrument on bereavement burden (PG- 13)
AnxietyBaselinestandardized instrument on anxiety (GAD-7)
DepressionBaselinestandardized instrument on depression (PHQ-9)
Caregiving burdenBaselinestandardized instrument on caregiver symptoms (MIDOS-2).

Countries

Germany

Outcome results

None listed

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