Evidence map›Paper›PMID 42360018›Full record

ArticleHealth expectations : an international journal of public participation in health care and health policy2026

Impact of a Health Research Training Program on Patient and Community Partners, and Researchers: A Qualitative Evaluation.

Sadia Ahmed, Ingrid Nielssen, Iqmat Iyiola, Paul Fairie, Sandra Munro, Maria J Santana

Abstract read
In one paragraph

Article in Health expectations : an international journal of public participation in health care and health policy, 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

6 authors.

Sadia AhmedAlberta Strategy for Patient Oriented Research, University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-8040-7198
Ingrid NielssenAlberta Strategy for Patient Oriented Research, University of Calgary, Calgary, AB, Canada.ORCID 0000-0003-3402-1611
Iqmat IyiolaFaculty of Agricultural, Life, and Environmental Sciences, University of Alberta, Edmonton, AB, Canada.
Paul FairieAlberta Strategy for Patient Oriented Research, University of Calgary, Calgary, AB, Canada.
Sandra MunroAlberta Strategy for Patient Oriented Research, University of Calgary, Calgary, AB, Canada.
Maria J SantanaAlberta Strategy for Patient Oriented Research, University of Calgary, Calgary, AB, Canada.

Funding

Alberta Strategy for Patient-Oriented Research
6 · The paper itself

Abstract

backgroundBuilding capacity through training and education is recommended to support meaningful engagement of patient partners in health research. The Patient and Community Engagement Research (PaCER) programme is a 12-month initiative that enables patients and community members to co-design and conduct qualitative health research projects. Learners are sponsored by clinician researchers, community organisations, and/or jurisdictional health organisations. This study aimed to assess the experiences and impact of the PaCER programme on: (1) past learners' personal development and engagement in health research; and (2) sponsors' research programmes.

methodsWe conducted a qualitative impact evaluation involving past learners (alumni) and sponsors of the PaCER programme from 2019 to 2024. A purposive sampling strategy was used, whereby selected alumni and sponsors from the 2019-2024 cohorts were invited to participate in an online semi-structured interview. Sponsors and alumni with diverse characteristics, including variation in age, ethnicity, educational attainment, and geographic location were invited. The interview guide included questions on the experiences in the PaCER programme, post-programme research activities, and perceptions of the programme's impact. Data were analysed using a reflexive thematic analysis approach.

resultsEighteen participants (12 PaCER alumni and 6 sponsors) were interviewed, and four main themes were identified: (1) seeing the value of the training programme; (2) Diverse people and groups working together; (3) Learner readiness and capacity; (4) Academic opportunities for learners and career growth. Alumni described significant personal impact, empowerment, academic contributions, and increased access to meaningful patient partner opportunities. Alumni reported co-authoring publications and presenting their work at academic conferences and to various stakeholders, including health system leadership. Many alumni had no prior experience with qualitative participatory research, and participation in the programme supported the development of these research skills. Sponsors also noted impacts on their research programmes, such as securing additional funding informed by PaCER project findings.

conclusionThe findings demonstrate that structured, experiential training for patients and community members supports meaningful engagement in health research, contributes to sustained capacity development, and positively influences the patient-oriented research landscape. PATIENT OR PUBLIC CONTRIBUTION: Patient partners were involved in the design and conduct of the study (data collection), analysis and interpretation of the data, and in the preparation of this manuscript.

Indexed as

Community-Based Participatory ResearchPatient ParticipationResearch PersonnelAdultCapacity BuildingFemaleHumansInterviews as TopicMaleMiddle AgedProgram EvaluationQualitative Researchimpact evaluationpatient‐oriented researchpatient partner trainingtraining programme

Identifiers

PMID42360018
PMCPMC13307345

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.