Evidence map›Paper›PMID 40171552›Full record

ArticlePalliative care and social practice2025

Neuropalliative care for Parkinson's disease in India: a qualitative exploration of healthcare professionals' perspectives.

Prerna Sharma, Upasana Baruah, Suman Kushwaha, Akanksha Yadav, Rajinder K Dhamija

Abstract read
In one paragraph

Article in Palliative care and social practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

1 citing paper in PubMed.

  1. Review
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.

Prerna SharmaDepartment of Clinical Psychology, Institute of Human Behaviour and Allied Sciences, New Delhi, India.ORCID https://orcid.org/0000-0002-9025-5431
Upasana BaruahDepartment of Psychiatric Social Work, Institute of Human Behaviour and Allied Sciences, New Delhi, India.ORCID https://orcid.org/0000-0002-5569-3970
Suman KushwahaDepartment of Neurology, Institute of Human Behaviour and Allied Sciences, New Delhi, India.ORCID https://orcid.org/0000-0003-1446-903X
Akanksha YadavDepartment of Clinical Psychology, Institute of Human Behaviour and Allied Sciences, New Delhi, India.
Rajinder K DhamijaDeparment of Neurology, Institute of Human Behaviour and Allied Sciences, Dilshad Garden, New Delhi, Delhi 110095, India.ORCID https://orcid.org/0000-0001-6042-7469

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The prevalence of Parkinson's disease (PD) in India is roughly 10% of the global burden, which is a considerable public health concern. The burden on healthcare services in India is substantial due to the variations in PD prevalence and the country's large population. The unique cultural, ethnic, and social differences in India give rise to distinct needs among PD patients and their caregivers. Neuropalliative care (NPC) is an emerging subspecialty with a holistic approach that requires a unique skill set and the involvement of allied healthcare professionals who play a crucial role in providing integrated services. Aim: The objective of this study is to explore the experiences and perspectives of the primary and allied healthcare professionals working with persons with PD in India. Methods: The current study employed a qualitative, exploratory, inductive research design, using in-depth interviews with 15 primary and allied healthcare professionals who had more than 5 years of experience working with persons with PD. Participants worked in varied settings such as academic hospitals, rehabilitation services, and tertiary care hospitals. Results: The mean years of work experience for the participants were 7.5 ± 3.26 years with a mean number of 30.8 ± 14.8 patients with PD per month. Thematic analysis of the data revealed 5 main themes and 20 subthemes. The major themes revealed were understanding of NPC, the needs of patients and caregivers of PD, barriers and challenges, interventions for patients and caregivers, facilitators, and components of NPC for PD. Conclusion: To provide a structured stepped-care approach to managing PD, there is a need to understand the psychosocial and palliative care aspects of PD in patients and caregivers in the Indian context. Adequate training and resource allocation are needed for NPC to be adopted in clinical care.

Indexed as

allied healthcare professionalsneurodegenerative disorderneuro-palliative careParkinson’s diseasepsychosocial care

Identifiers

PMID40171552
PMCPMC11960147

What OpenQuestion holds

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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.