Evidence map›Paper›PMID 41637446›Full record

ArticlePloS one2026

Process evaluation of a hybrid effectiveness-implementation, pragmatic, cluster randomised controlled trial (IMPULSE) to improve psychosocial treatment of patients with psychotic-spectrum disorders in Southeast Europe.

Tamara Pemovska, Nikolina Jovanović, Tamara Radojičić, Silvana Markovska Simoska, Fjolla Ramadani, Sanja Andrić Petrović, Emina Karamehić, Biljana Blazhevska Stoilkovska, Jon Konjufca, Stefan Jerotić and 3 more

Abstract read
In one paragraph

Article in PloS one, 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
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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

13 authors.

Tamara PemovskaCentre for Evidence and Implementation, London, United Kingdom.ORCID https://orcid.org/0000-0003-4362-0165
Nikolina JovanovićCentre for Psychiatry and Mental Health, Wolfson Institute of Population Health, Queen Mary University of London, London, United Kingdom.ORCID https://orcid.org/0000-0002-7554-9837
Tamara RadojičićPsychiatric Clinic, Clinical Centre of Montenegro, Podgorica, Montenegro.
Silvana Markovska SimoskaMacedonian Academy of Sciences and Arts, Skopje, North Macedonia.
Fjolla RamadaniDepartment of Psychology, University of Prishtina, Prishtina, Kosovo United Nations Resolution.
Sanja Andrić PetrovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Emina KaramehićPublic Institution Department for Health Care of Women and Maternity of Sarajevo Canton, Sarajevo, Bosnia and Herzegovina.
Biljana Blazhevska StoilkovskaDepartment of Psychology, Faculty of Philosophy, Ss. Cyril and Methodius University in Skopje, Skopje, North Macedonia.ORCID https://orcid.org/0000-0002-8905-5301
Jon KonjufcaDepartment of Psychology, University of Prishtina, Prishtina, Kosovo United Nations Resolution.
Stefan JerotićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Alma Džubur KulenovićDepartment of Psychiatry, Clinical Centre of the University of Sarajevo, Sarajevo, Bosnia and Herzegovina.
Lidija Injac StevovićPsychiatric Clinic, Clinical Centre of Montenegro, Podgorica, Montenegro.
Jill J FrancisSchool of Health Sciences, University of Melbourne, Australia.ORCID https://orcid.org/0000-0001-5784-8895

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe IMPULSE trial investigated the effectiveness and implementation of a digital psychosocial intervention (DIALOG+) for people with psychosis in five Southeast European countries. DIALOG+ significantly improved patients' quality of life after four treatment sessions. The process evaluation reported here aimed to assess contextual influences on intervention delivery during the trial, to explain the trial findings and generate hypotheses about mechanisms of action by exploring acceptability from the perspectives of clinicians who delivered it and trial participants who received it, and fidelity (was the intervention delivered and received as planned?).

methodA mixed-methods process evaluation was conducted in accordance with the published protocol, guided by theoretical frameworks and the Medical Research Council's guidance for complex interventions. To explore the role of context, data were analysed about the participating services, policy documents, and from focus groups with key stakeholders. Semi-structured interviews with clinicians and patients were conducted to explore acceptability. Process data (format and content of sessions) were analysed to assess intervention fidelity. Data analysis included descriptive methods, framework and content analysis, and triangulation.

resultsSeveral attributes of context related to health services, including resource limitations, funding priorities, reliance on paper records and lack of community support, potentially negatively impacted DIALOG+ acceptability, fidelity and outcomes. Contextual enablers were also identified, including an appetite for change among key stakeholders that can help overcome contextual barriers. Acceptability of the psychosocial intervention was moderate to high and fidelity was high.

conclusionsIntervention acceptability is likely to have played a key role in ensuring high fidelity, which in turn likely contributed to the intervention's positive impact on patients' quality of life. The high fidelity confirms that the IMPULSE trial findings provide a valid assessment of the intervention as designed. While the identified contextual barriers appear not to have impaired intervention fidelity, acceptability and outcomes, they could pose challenges to the long-term sustainability of the intervention.

trial registrationRetrospectively registered on 29 March 2021, ISRCTN11913964.

Indexed as

Psychosocial InterventionPsychotic DisordersAdultEuropeFemaleFocus GroupsHumansMaleMiddle AgedPragmatic Clinical Trials as TopicQuality of LifeRandomized Controlled Trials as Topic

Identifiers

PMID41637446
PMCPMC12872023

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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.