Evidence map›Paper›PMID 42111022›Full record

ArticleNeuro-oncology practice2026

Current and bereaved caregivers' experiences of participating in the adapted Telehealth Making Sense of Brain Tumour program in the context of high-grade glioma.

Abigail Billin, Katarzyna M Lion, Stephanie Jones, Mark B Pinkham, Georgia K B Halkett, Haryana M Dhillon, Tamara Ownsworth

Abstract read
In one paragraph

Article in Neuro-oncology practice, 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
–field-weighted citation impact
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.

Abigail BillinThe Hopkins Centre, Griffith University, Queensland, Australia.
Katarzyna M LionThe Hopkins Centre, Griffith University, Queensland, Australia.ORCID https://orcid.org/0000-0002-3699-6896
Stephanie JonesThe Hopkins Centre, Griffith University, Queensland, Australia.
Mark B PinkhamDepartment of Radiation Oncology, Princess Alexandra Hospital, Queensland, Australia.ORCID https://orcid.org/0000-0001-8886-728X
Georgia K B HalkettSchool of Nursing, Faculty of Health Sciences, Curtin University, Perth, Western Australia, Australia.ORCID https://orcid.org/0000-0003-4065-4044
Haryana M DhillonPsycho-Oncology Cooperative Research Group, School of Psychology, Faculty of Science, University of Sydney, Sydney, New South Wales, Australia.ORCID https://orcid.org/0000-0003-4039-5169
Tamara OwnsworthThe Hopkins Centre, Griffith University, Queensland, Australia.ORCID https://orcid.org/0000-0003-1835-7094

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Telehealth Making Sense of Brain Tumour program (Tele-MAST) was adapted for caregivers (cTele-MAST) to address the lack of caregiver-specific psychological support interventions in the context of high-grade glioma. This study aimed to explore current and bereaved caregivers' reasons for seeking psychological support, experiences of participating in cTele-MAST, and impacts on mental health and quality of life. Methods: A longitudinal multi-methods design was employed, capturing qualitative and quantitative data prior to cTele-MAST (Time 1), 1-week (Time 2), and 3-month post-intervention (Time 3). Qualitative data were analyzed using reflexive thematic analysis and quantitative data using repeated measures ANOVA. Participants were offered individual cTele-MAST sessions via videoconferencing and completed semi-structured interviews and measures of mental health and quality of life (QoL). Eighteen caregivers (15 female, Results: Three themes were identified. "Caregiver expectations of the self" reflected a desire to become stronger, more resilient, and quickly adapt their lives around caregiving. "Enabling, connecting and reframing" represented perceived benefits of cTele-MAST in terms of accessibility, brain tumor-specific expertise, and support to reset self-expectations. "Finding one's self" reflected caregivers better acknowledging their own needs and understanding themselves in grief. Significant post-intervention reductions in distress and stress were evident, but not for depression, anxiety or QoL. Conclusions: Caregivers found participating in a psychological support program tailored to their needs beneficial. Early referral to cTele-MAST and flexible ongoing access to psychological support is recommended.

Indexed as

brain cancercaregiver burdencaregiverspalliative carepsychosocial supportquality of life

Identifiers

PMID42111022
PMCPMC13153700

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.