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ArticleJMIR research protocols2026

Psychosocial Burden and Supportive Care Needs of Informal Caregivers in Specialist Palliative Care: Protocol of a Multicenter Longitudinal Cohort Study to Identify Trajectories and Validate the Multidimensional Screening Tool CAREPAL-8.

Clara Haufschild, Karin Oechsle, Antonia Zapf, Anne Daubmann, Philipp Weber, Holger Schulz, Anneke Ullrich

Abstract readMulticenter Study
In one paragraph

Article in JMIR research protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Clara HaufschildPalliative Medicine, Department of Oncology, Hematology and BMT, University Medical Center Hamburg-Eppendorf, Martinistraße 52, Hamburg, 20246, Germany, 49 40741055690.ORCID 0000-0001-9359-6576
Karin OechslePalliative Medicine, Department of Oncology, Hematology and BMT, University Medical Center Hamburg-Eppendorf, Martinistraße 52, Hamburg, 20246, Germany, 49 40741055690.ORCID 0000-0002-5183-641X
Antonia ZapfInstitute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-8467-0508
Anne DaubmannInstitute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0003-0156-0926
Philipp WeberInstitute of Medical Biometry and Epidemiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0002-9520-6284
Holger Schulz *Department of Medical Psychology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.ORCID 0000-0001-5375-0030
Anneke Ullrich *Palliative Medicine, Department of Oncology, Hematology and BMT, University Medical Center Hamburg-Eppendorf, Martinistraße 52, Hamburg, 20246, Germany, 49 40741055690.ORCID 0000-0002-1759-4461

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Informal caregivers (ICs) of patients with advanced incurable diseases experience substantial psychosocial burden and unmet needs. However, efficient screening tools to identify ICs at risk of developing clinically relevant psychosocial problems are lacking. Additionally, most existing studies on burden and needs use cross-sectional designs, failing to capture the dynamic and evolving nature of caregiving. Objective: This study aims (1) to explore the trajectories of ICs' psychosocial burden and supportive care needs during specialist palliative care (SPC) and factors associated with these trajectories and (2) to validate the 8-Item Screening Tool for Family Caregiver Burden in Palliative Care (CAREPAL-8), an 8-item multidimensional screening tool developed to categorize ICs into clinically relevant risk groups regarding dimensions of burden. Methods: This prospective, multicenter, longitudinal cohort study is conducted across 16 study centers in Germany, involving palliative care wards, multiprofessional SPC teams in hospitals, and specialist palliative home care teams. Data are collected upon the patient's admission to SPC (baseline) and weekly for up to 10 weeks, using validated questionnaires and the CAREPAL-8. Based on a priori sample size calculation, we aim to collect data from 510 ICs at baseline and on at least 1 additional follow-up measurement point. To minimize participant burden, a planned missing data design is used for follow-up questionnaires. Data analyses will include growth mixture models for study aim 1 and determination of convergent validity and sensitivity to change of the CAREPAL-8 for study aim 2. Results: Data collection commenced on July 31, 2023. Results are expected from March 2026. Conclusions: This study aims to provide comprehensive insights into the trajectories of IC burden and needs in SPC. The validation of the CAREPAL-8 could offer a brief screening tool to classify ICs according to different risk profiles, enabling targeted support. Furthermore, the planned missing data design may enhance data quality while reducing participant burden, potentially serving as a model for similar studies in vulnerable populations.

Indexed as

CaregiversMass ScreeningPalliative CareGermanyHumansLongitudinal StudiesProspective StudiesPsychometricsSurveys and Questionnairesinformal caregiverspsychosocial burdensscreeningspecialist palliative caresupportive care needstrajectory

Identifiers

PMID42536973
PMCPMC13427073

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