Evidence map›Paper›PMID 42581101›Full record

ArticleEuropean journal of human genetics : EJHG2026

Holding the story, holding the professional: a pilot study of genetic counselling supervision in Portugal.

Lídia Guimarães, Mariangels Ferrer-Duch, Inês Costa, Ane Sagardia, Maria Ramos-Arroyo, Fernando Alvira-Iraizoz, María Tubío-Fungueiriño, Montse Fernández-Prieto, Nelly Pasz, Pauline Villa and 2 more

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Article in European journal of human genetics : EJHG, 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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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

12 authors.

Lídia Guimarães *i3S-Institute for Research and Innovation in Health, University of Porto, Porto, Portugal.ORCID http://orcid.org/0000-0002-3229-5785
Mariangels Ferrer-Duch *Faculty of Biology, Medicine, and Health, University of Manchester, Manchester, UK.ORCID http://orcid.org/0000-0002-0157-6306
Inês Costai3S-Institute for Research and Innovation in Health, University of Porto, Porto, Portugal.ORCID http://orcid.org/0009-0006-7855-1189
Ane SagardiaDepartamento de Genética Médica, Hospital Universitario de Navarra, Navarra, Spain.ORCID http://orcid.org/0000-0002-4732-4067
Maria Ramos-ArroyoUnidad de Neurogenetica. Navarrabiomed, Universidad Pública de Navarra (UPNA), Hospital Universitario de Navarra, Instituto de Investigación Sanitaria de Navarra (IdiSNA), Navarra, Spain.ORCID http://orcid.org/0000-0002-7171-9202
Fernando Alvira-IraizozGenomics Medicine Unit, Navarrabiomed, Public University of Navarra (UPNA), Navarra University Hospital (HUN), Navarra Institute for Health Research (IdisNA), Navarra, Spain.ORCID http://orcid.org/0000-0001-8324-6409
María Tubío-FungueiriñoFundación Pública Galega Instituto de Investigación Sanitaria de Santiago de Compostela (FIDIS), Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0002-8121-2472
Montse Fernández-PrietoFundación Pública Galega Instituto de Investigación Sanitaria de Santiago de Compostela (FIDIS), Santiago de Compostela, Spain.ORCID http://orcid.org/0000-0003-3800-9476
Nelly PaszService de Génétique clinique, Centre Hospitalier Universtaire de Toulouse, Toulouse, France.ORCID http://orcid.org/0009-0007-8335-8145
Pauline VillaService de Génétique clinique, Centre Hospitalier Universtaire de Toulouse, Toulouse, France.ORCID http://orcid.org/0009-0004-2275-5604
Margarida Rangel HenriquesFPCEUP-Faculty of Psychology and Educational Sciences. University of Porto, Porto, Portugal.ORCID http://orcid.org/0009-0001-6059-6710
Milena Panequei3S-Institute for Research and Innovation in Health, University of Porto, Porto, Portugal. milenaph@ibmc.up.pt.ORCID http://orcid.org/0000-0002-6535-4315

Funding

EC | Europski Fond za Regionalni Razvoj | Interreg S2/4.5/P0159
6 · The paper itself

Abstract

The increasing complexity of genomic medicine has intensified the emotional, ethical, and relational demands placed on genetic counselling professionals. In response to these demands, genetic counselling supervision has been increasingly recognised as a core component of safe and sustainable practice. However, its implementation across Europe remains uneven, and empirical evidence on feasible and acceptable supervision models in clinical settings is limited. This study reports a mixed-methods pilot evaluation of a narrative-informed, group-based genetic counselling supervision programme implemented within Portuguese public genetic services. This is a foundational component of the first phase of the MAG-SUDOE project, a transnational initiative supported by the Interreg SUDOE programme aimed at developing a joint supervision solution for genetic counselling professionals in Portugal, Spain, and France. Eight genetic healthcare professionals were recruited, and seven completed the intervention. Feasibility and acceptability were examined through participation and attendance rates, session evaluations, and assessment of the supervisory working alliance. Preliminary impact was explored using self-report measures of psychological well-being and perceived counselling quality, complemented by qualitative data from written narratives, semi-structured interviews, and a final focus group. The programme demonstrated high feasibility, with strong engagement and completion despite clinical workload constraints, and high acceptability, reflected in positive session evaluations and strong supervisory working alliance. Qualitative findings indicated that participants experienced supervision as a safe and reflective space that reduced isolation, supported emotional regulation, and enhanced reflective awareness. Overall, this pilot study provides promising indications of benefit for reflective practice and professional well-being, supporting its further adaptation and implementation within a transnational European framework.

Identifiers

PMID42581101

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Registered trials

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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.