Evidence map›Paper›PMID 42204079›Full record

ArticleInternational journal of behavioral medicine2026

A Qualitative Study Exploring Psychosocial Care in Inflammatory Bowel Disease: Lessons from Aotearoa New Zealand.

Sancharya Pahwa MHealthPsyc, Annie S K Jones, Sian Ellett MHealthPsyc, Katie Babbott, Anna Serlachius

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Article in International journal of behavioral medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited 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

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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

5 authors.

Sancharya Pahwa MHealthPsycUniversity of Auckland, Auckland, New Zealand.
Annie S K JonesUniversity of Auckland, Auckland, New Zealand.
Sian Ellett MHealthPsycUniversity of Auckland, Auckland, New Zealand.
Katie BabbottUniversity of Auckland, Auckland, New Zealand.
Anna SerlachiusUniversity of Auckland, Auckland, New Zealand. a.serlachius@auckland.ac.nz.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExisting evidence demonstrates that inflammatory bowel disease (IBD) profoundly impacts physical, psychosocial, and emotional well-being, yet psychosocial support is limited in routine care in Aotearoa New Zealand (NZ). This qualitative study aimed to explore the lived experience of adults with IBD in NZ, focusing on psychosocial challenges and patient-driven recommendations for improving support during diagnosis and disease management.

methodTwelve adults with IBD participated in semi-structured interviews as part of a nested qualitative study. Data were analysed using the framework method of thematic analysis to identify key patterns in participants' experiences.

resultsFour main themes reflected the experience of being diagnosed with IBD: (1) trust and mistrust, (2) care not cure, (3) educate, adhere, empower, and (4) dynamics of coping and adjustment. Participants described difficulties navigating the healthcare system, coping with changes in body and identity, and managing the psychological burden of living with a chronic illness. A consistent lack of integrated psychosocial support was reported. Participants emphasised the need for improved health literacy, support for medication adherence, and tailored psychological care. Their suggestions underscored the importance of embedding psychosocial services within routine IBD management.

conclusionsAdults with IBD in NZ face substantial psychosocial challenges that are not adequately addressed in current care models. Integrating psychosocial support into routine IBD care could alleviate patient burden and enhance health system responsiveness. These findings offer critical insights for developing more holistic, patient-centred approaches to IBD care in NZ and similar healthcare contexts.

Indexed as

Framework methodInflammatory bowel diseasePsychosocial supportQualitative studyThematic analysis

Identifiers

PMID42204079

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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.