Evidence map›Paper›PMID 38486810›Full record

ArticleNeurology. Clinical practice2024

Delivering Genetic Test Results for Parkinson Disease: A Qualitative Approach to Provider Experiences in the PD GENEration Study.

Mandy Miller, Lola Cook, Jennifer Verbrugge, Priscila D Hodges, Katharine J Head, Martha A Nance

Registry-linked trialAbstract read
In one paragraph

Article in Neurology. Clinical practice, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04057794 (Parkinson's Foundation), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT04057794 naunknown statusnot on this map

Parkinson's Foundation: PD Generation: Mapping the Future of Parkinson's Disease

TypeinterventionalSponsorParkinson's FoundationRan2019 to 2025Enrolled1,982ConditionsParkinson's Disease and ParkinsonismArmsLab Assay for seven genetic variants for Parkinson's Disease
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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.

Mandy MillerDepartment of Medical and Molecular Genetics (MM, LC, JV, PDH), Indiana University School of Medicine; Department of Communication Studies (KJH), Indiana University-Purdue University Indianapolis; and Struthers Parkinson's Center (MAN), Minneapolis, MN.ORCID https://orcid.org/0009-0000-0750-0719
Lola CookDepartment of Medical and Molecular Genetics (MM, LC, JV, PDH), Indiana University School of Medicine; Department of Communication Studies (KJH), Indiana University-Purdue University Indianapolis; and Struthers Parkinson's Center (MAN), Minneapolis, MN.ORCID https://orcid.org/0000-0001-6109-4598
Jennifer VerbruggeDepartment of Medical and Molecular Genetics (MM, LC, JV, PDH), Indiana University School of Medicine; Department of Communication Studies (KJH), Indiana University-Purdue University Indianapolis; and Struthers Parkinson's Center (MAN), Minneapolis, MN.ORCID https://orcid.org/0000-0003-2778-2762
Priscila D HodgesDepartment of Medical and Molecular Genetics (MM, LC, JV, PDH), Indiana University School of Medicine; Department of Communication Studies (KJH), Indiana University-Purdue University Indianapolis; and Struthers Parkinson's Center (MAN), Minneapolis, MN.ORCID https://orcid.org/0000-0002-8530-5449
Katharine J HeadDepartment of Medical and Molecular Genetics (MM, LC, JV, PDH), Indiana University School of Medicine; Department of Communication Studies (KJH), Indiana University-Purdue University Indianapolis; and Struthers Parkinson's Center (MAN), Minneapolis, MN.ORCID https://orcid.org/0000-0001-8946-1716
Martha A NanceDepartment of Medical and Molecular Genetics (MM, LC, JV, PDH), Indiana University School of Medicine; Department of Communication Studies (KJH), Indiana University-Purdue University Indianapolis; and Struthers Parkinson's Center (MAN), Minneapolis, MN.ORCID https://orcid.org/0000-0003-4994-8815

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: The PD GENEration (PD GENE) study (NCT04057794) is an interventional clinical trial offering genetic testing with result disclosure and genetic counseling to individuals with Parkinson disease (PD). In general, experiences of those providing PD genetic testing and counseling in a research or clinical setting have not been extensively evaluated. In this study, providers' experiences when providing research result disclosure and genetic counseling to people with PD were explored with the goal of improving PD genetics services. Methods: Qualitative semistructured interviews of all neurologists and genetic counselors who performed genetic test result disclosure and genetic counseling to at least 5 participants in the pilot portion of the PD GENE study were conducted. An inductive thematic analysis of the transcribed interviews identified core themes and subthemes for "lessons learned" and "challenges encountered." Results: Interviews were conducted with 14 providers (7 neurologists and 7 genetic counselors) who described multiple lessons learned while disclosing genetic test results, including the ability to adapt to participant background and needs and the value of a well-structured and supportive study that also provides training and educational materials for the provider. Of importance, responses suggested that the PD GENE study answered a real need, highlighting a strong interest in the community. Providers also voiced several shared challenges including the complexities of PD and PD genetics, unexpected confusion on provider roles within a research study, and complicated family histories/dynamics. Discussion: Providers in the pilot portion of the PD GENE study encountered enthusiasm and strong engagement from many of the participants, and they, too, voiced significant satisfaction about their roles and the mission of the study. They learned valuable lessons, and their comfort providing genetic test result disclosure and genetic counseling grew as the study progressed. Although there were challenges, they were deemed manageable. The results from this qualitative study can inform both the expanded PD GENE study and other providers offering genetic testing and counseling to their patients in a neurology setting. It will also allow for targeted PD provider education.

Identifiers

PMID38486810
PMCPMC10932733

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Registered trials

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.