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Exploring Stress and Stress-Reduction With Caregivers and Clinicians in the Neonatal Intensive Care Unit to Inform Intervention Development: Qualitative Interview Study

Exploring Stress and Stress-Reduction With Caregivers and Clinicians in the Neonatal Intensive Care Unit to Inform Intervention Development: Qualitative Interview Study

We sought to collect a range of perspectives on caregiver stress and support in the NICU, so we recruited both currently admitted and discharged parents and legal guardians of preterm babies in the NICU. We also aimed to include other types of caregivers in this study, such as extended family members who had spent significant time in the NICU.

Kristin Harrison Ginsberg, Jane Alsweiler, Jenny Rogers, Phoebe Ross, Anna Serlachius

JMIR Pediatr Parent 2025;8:e66401

Cooperative Virtual Reality Gaming for Anxiety and Pain Reduction in Pediatric Patients and Their Caregivers During Painful Medical Procedures: Protocol for a Randomized Controlled Trial

Cooperative Virtual Reality Gaming for Anxiety and Pain Reduction in Pediatric Patients and Their Caregivers During Painful Medical Procedures: Protocol for a Randomized Controlled Trial

If a medical procedure causes intense fear or pain, it can strain the caregiver-child relationship, especially if the child perceives the caregivers as siding with medical staff instead of supporting them—for example, by helping to physically restrain the child [7]. As a result, anxiety, stress, and pain of patient and caregiver can mutually depend on and reinforce each other [8].

Stefan Liszio, Franziska Bäuerlein, Jens Hildebrand, Carolin van Nahl, Maic Masuch, Oliver Basu

JMIR Res Protoc 2025;14:e63098

Employers’ Perspectives of Caregiver-Friendly Workplace Policies for Caregiver-Employees Caring for Older Adults in Hong Kong: Thematic Analysis

Employers’ Perspectives of Caregiver-Friendly Workplace Policies for Caregiver-Employees Caring for Older Adults in Hong Kong: Thematic Analysis

Although several studies have identified caregiver burden as a significant risk factor for burnout and poor mental health outcomes among family caregivers [11,13,14], stronger filial piety may lead to lower caregiver burden [15,16]. A systematic review of 12 studies showed a significant negative correlation (r=–0.23) and association (β=–0.27) between filial piety and caregiver burden among adult children [15].

Maggie Man-Sin Lee, Eng-Kiong Yeoh, Eliza Lai-Yi Wong

JMIR Aging 2025;8:e68061

Assessment of Health System Readiness and Quality of Dementia Services in Peru: Protocol for a Qualitative Study With Stakeholder Interviews and Documentation Review

Assessment of Health System Readiness and Quality of Dementia Services in Peru: Protocol for a Qualitative Study With Stakeholder Interviews and Documentation Review

Specific challenges for the health systems and people with dementia include developing effective diagnostic services, managing cognitive and behavioral decline, handling multiple comorbidities, caregiver burden, widespread stigma, and lack of awareness about dementia. The concept of tracer conditions can help facilitate understanding the complexity of health systems and the challenges LMICs face [7,8].

Maria Lazo-Porras, Francisco Jose Tateishi-Serruto, Christopher Butler, María Sofía Cuba-Fuentes, Daniela Rossini-Vilchez, Silvana Perez-Leon, Miriam Lúcar-Flores, J Jaime Miranda, Antonio Bernabe-Ortiz, Francisco Diez-Canseco, Graham Moore, Filipa Landeiro, Maria Kathia Cardenas, Juan Carlos Vera Tudela, Lee White, Rafael A Calvo, William Whiteley, Jemma Hawkins, IMPACT Salud Study Group

JMIR Res Protoc 2025;14:e60296

Using Wear Time for the Analysis of Consumer-Grade Wearables’ Data: Case Study Using Fitbit Data

Using Wear Time for the Analysis of Consumer-Grade Wearables’ Data: Case Study Using Fitbit Data

By leveraging a broad array of datasets, including vulnerable patient populations, we showed evidence of the nuanced effect of wear time, highlighting its critical role in research using wearables, especially in samples with inconsistent wear patterns such as the pediatric oncology caregiver and patient participants used in this study. It is important to note that the pediatric oncology patients’ ages ranged from 5 to 20 years, with a mean of 11.9 years.

Loubna Baroudi, Ronald Fredrick Zernicke, Muneesh Tewari, Noelle E Carlozzi, Sung Won Choi, Stephen M Cain

JMIR Mhealth Uhealth 2025;13:e46149

On the Necessity of Multidisciplinarity in the Development of at-Home Health Monitoring Platforms for Older Adults: Systematic Review

On the Necessity of Multidisciplinarity in the Development of at-Home Health Monitoring Platforms for Older Adults: Systematic Review

Overall, 13.7% and 64.2% of single-discipline papers involve end user participation versus a mere 14.2% and 0% exhibiting caregiver or medical participation in the development of the research (for application and technical based papers. respectively).

Chris Lochhead, Robert B Fisher

JMIR Hum Factors 2025;12:e59458

Evaluation of the Quality of Delirium Website Content for Patient and Family Education: Cross-Sectional Study

Evaluation of the Quality of Delirium Website Content for Patient and Family Education: Cross-Sectional Study

Reference 3: Translating evidence to patient care through caregivers: a systematic review of caregiver-mediated Reference 11: Associations between hospice care and scary family caregiver experiencescaregiver

Karla Krewulak, Kathryn Strayer, Natalia Jaworska, Krista Spence, Nadine Foster, Scotty Kupsch, Khara Sauro, Kirsten M Fiest

J Med Internet Res 2025;27:e53087

Traversing Shifting Sands—the Challenges of Caring for Someone With Alzheimer's Disease and the Impact on Care Partners: Social Media Content Analysis

Traversing Shifting Sands—the Challenges of Caring for Someone With Alzheimer's Disease and the Impact on Care Partners: Social Media Content Analysis

Reference 9: Caregiver burden and prevalence of depression, anxiety and sleep disturbances in Alzheimer's Reference 12: Caregiver burden in Alzheimer-type dementia and psychosis: a comparative study from Indiacaregiver

Kristian Steen Frederiksen, Julie Hahn-Pedersen, Rebecca Crawford, Ross Morrison, Rose Jeppesen, Lynda Doward, Wendy Weidner

J Med Internet Res 2025;27:e55468

Uncovering Specific Navigation Patterns by Assessing User Engagement of People With Dementia and Family Caregivers With an Advance Care Planning Website: Quantitative Analysis of Web Log Data

Uncovering Specific Navigation Patterns by Assessing User Engagement of People With Dementia and Family Caregivers With an Advance Care Planning Website: Quantitative Analysis of Web Log Data

Beyond this evaluation, gaining insights into the website’s user engagement and usage patterns is crucial to enhance our understanding of how people with dementia and their families use a website to support advance care planning in the family context, how they engage with it and how single users and dyadic users differ (ie, people with dementia together with their family caregiver).

Charlèss Dupont, Tinne Smets, Courtney Potts, Fanny Monnet, Lara Pivodic, Aline De Vleminck, Chantal Van Audenhove, Maurice Mulvenna, Lieve Van den Block

JMIR Aging 2025;8:e60652