Qualitative Health Research

Papers
(The median citation count of Qualitative Health Research is 2. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-04-01 to 2025-04-01.)
ArticleCitations
Guardians Looking From Outside: Gendered Experiences of Labor Migration and Psychosocial Health Among Nepalese Migrant Fathers and Left-Behind Mothers81
Ethnography in Health Services Research: Oscillation Between Theory and Practice68
Corrigendum to “A Prospective Qualitative Inquiry of Patient Experiences of Cognitive Functional Therapy for Chronic Low Back Pain During the RESTORE Trial”50
Photovoice and Instagram as Strategies for Youth Engagement in Disaster Risk Reduction47
Through the Eyes of a Young Carer: A Photo Elicitation Study of Protective Resilience46
Ethical Consequences of Technological Mediation on Parental Decision-Making Experiences in the Neonatal Intensive Care Unit40
Jarring Encounters: Discomfort, Disruption, and Dominant Narratives of Suicide39
I’m Skinny, I’m Worth More: Fashion Models’ Experiences of Aesthetic Labor and Its Impact on Body Image and Eating Behaviors35
Emerging Dilemmas in the Age of Resistance: The Case of Sexually Transmitted Infections30
A Pianist’s Technique Rehabilitation After Post-Traumatic Stress: An Autoethnographic Study28
“Because of HIV, It Opened My Mind”: Intersectional Stigma Experiences Among Filipino Gay and Bisexual Men Living With HIV28
A Participatory Evaluation of an Urban Garden Project in Ecuador: Exploring Factors That Impact the Recovery of People With Severe Mental Health Problems27
“Sewing Is Part of Our Tradition”: A Case Study of Sewing as a Strategy for Arts-Based Inquiry in Health Research With Inuit Women27
“The Videos Gave Weight to Our Work”: Animated mHealth Videos and Tablet Technology Boost Community Health Workers’ Perceived Credibility in Khayelitsha, South Africa25
Striving for Improved Infection Prevention and Control Practice: A Grounded Theory of Healthcare Workers’ Struggles in Implementing Infection Prevention and Control Guidance in Uganda24
From Promise to Practice: How Health Researchers Understand and Promote Transdisciplinary Collaboration23
Theorising Support for Interdisciplinary Early-Career Researchers Using Communicative Genre and ‘Rules of the Game’23
Digital Storytelling as a Patient Engagement and Research Approach With First Nations Women: How the Medicine Wheel Guided Our Debwewin Journey22
Participatory Action Research Among People With Serious Mental Illness: A Scoping Review22
Protecting Personhood: A Classic Grounded Theory22
“You Probably Won’t Notice Any Symptoms”: Blood Pressure in Pregnancy—Discourses of Contested Expertise in an Era of Self-Care and Responsibilization22
“If not me, who?”: Awareness- and Self-Advocacy-Related Experiences of Adults With Diverse Rare Disorders22
“I’m Not Comfortable With COVID, But …”: Dilemmas and Decision-Making to Mitigate Risks Among Mothers Who Gave Birth During the COVID-19 Pandemic22
Enacting Woundedness and Compassionate Care for Recurrent Metastatic Breast Cancer22
Social Influences on Engagement With HIV Testing, Treatment and Care Services Among Men Who Have Sex With Men Living in Rural Uganda21
A Prospective Qualitative Inquiry of Patient Experiences of Cognitive Functional Therapy for Chronic Low Back Pain During the RESTORE Trial20
HIV Diagnosis as Both Biographical Disruption and Biographical Reinforcement: Experiences of HIV Diagnoses Among Recently Diagnosed People Living With HIV20
A Qualitative Model of Weight Cycling20
The “Be All and End All”? Young People, Online Sexual Health Information, Science and Skepticism19
Comparing Patients’ Experiences in Three Differentiated Service Delivery Models for HIV Treatment in South Africa18
A Scholar of Hope: Norman Denzin and His Legacy for QHR18
‘You Are Kind of Like One of Us’: Exploring Researcher Positioning in Studying Community-Based Health Promotion Interventions Among Social Housing Residents of Danish, Turkish and Pakistani Origin18
Intraprofessionalism and Peer-to-Peer Learning in American Medical Education17
Seeing Red: A Grounded Theory Study of Women’s Anger after Childbirth17
Sero-Kinship: How Young People Living With HIV/AIDS Survive in Southeast Nigeria17
Introducing SAMMSA, a Five-Step Method for Producing ‘Quality’ Qualitative Analysis16
Patient Flow or the Patient’s Journey? Exploring Health Care Providers’ Experiences and Understandings of Implementing a Care Pathway to Improve the Quality of Transitional Care for Older People16
Mothering a Child With Complexity and Rarity: A Narrative Inquiry Exploring Prader-Willi Syndrome16
Emotions and Narrative Reappraisal Strategies of Users of Breast Cancer Screening: Reconstructing the Past, Passing Through the Present, and Predicting Emotions16
Experimental (Re)structuring: The Clinical Trial as Turning Point Among Medical Research Participants15
How Person-Centred Is Cardiac Rehabilitation in England? Using Bourdieu to Explore Socio-Cultural Influences and Personalisation15
The Voices of Stakeholders Involved in Precision Medicine: The Co-Design and Evaluation of Qualitative Indicators of Intervention Acceptability, Fidelity and Context in PRecISion Medicine for Children15
Health Experiences of Women University Students of Color and Women International Students in the United States During the First Year of the COVID-19 Pandemic: Findings From a Transnational, Virtual Ph15
A Qualitative Study of Aboriginal Peoples’ Health Care Experiences With Chronic Obstructive Pulmonary Disease14
In Pursuit of a Person-Centered Approach to Care Delivery: A Qualitative Descriptive Study of the Patient Experience of a Long-Term Conditions Clinic in General Practice14
Cultural Bereavement and Resilience in Refugee Resettlement: A Photovoice Study With Yazidi Women in the Midwest United States14
“Somewhere Between an Actual Disease and a Disease”: A Grounded Theory Study on Diagnosing Functional Neurological Disorders From a Multi-Informant Perspective14
The Online Representation of Palliative Care by Practice, Policy, and Advocacy Organizations: Definitional Variations and Discursive Tensions14
Reaching a Tipping Point: A Qualitative Exploration of Quality of Life and Treatment Decision-Making in People Living With Benign Prostatic Hyperplasia14
The Life-Course Perspectives of Mexican American Men With Mobility Limitation13
“It’s Like Youth are Talking Into a Microphone That is not Plugged in”: Engaging Youth in Disaster Risk Reduction Through Photovoice13
Exploration of Family-Centered Care in NICUs: A Grounded Theory Methodology13
Moving on From the Delphi Study: The Development of a Physical Activity Training Programme Prototype Through Co-produced Qualitative Research13
“You Do It Through the Grapevine”: A Bourdieusian Analysis of Under-Age Access to Tobacco Among Adolescents From Seven European Cities13
Global Voices of Trauma Recovery: A Synthesis of Survivor-Provided Advice for Overcoming Gender-Based Violence Across Seven Countries13
Protecting Anonymity in Rural Locales: The Use of Composite Narratives in Intimate Partner Violence Research13
“Switching Hats”: Insights From Experienced Clinical Interviewers Turned Novice Research Interviewers13
“That Is What We Have Left of Her”: The Significance of Transitional Objects After the Death of an Infant in a Norwegian Context13
“Now You Get to See Me”: Black Women Healthcare Professionals’ Experiences in Sister Circles During the Double Pandemic12
Treatment Pressures and the Predicament of Family Care: A Grounded Theory Study With Relatives of People With a Serious Mental Health Condition12
The Help-Seeking Experiences of Family and Friends Who Support Young People With Mental Health Issues: A Qualitative Study12
Lessons Learned From a Knowledge-Matching Participatory Research Approach Involving Law Students and Older Adults as Peer Researchers12
“Instead of Building More Buildings, They Should Plant More Trees”, a Photovoice Study of Determinants of Happiness and Sadness Among East London Adolescents12
Being Uncertain: Rural-Living Cardiac Patients’ Experience of Seeking Health Care12
“Sense for Gambling” Among Jewish Ultra-Orthodox Men With Gambling Disorder12
Black Queer Being/Knowing/Feeling: Storytelling of Barriers to Reproductive Healthcare12
A Qualitative Study on Psychosocial Challenges of Patients With Cancer in Ethiopia Using the Social-Ecological Model12
Complaining, Regret, Superiority, and Discovery: Chinese Patients’ Sense Making of Depression in an Online Forum12
Identifying Factors that Support the Delivery of Exceptional Care in General Practice and Development of the IDEAL Framework: A Qualitative Study12
The Sensory Experience of Waiting for Parents of Children Awaiting Transplant: A Narrative Ethnography11
Sensing Sociality: Disruptions of Social Life When Living With Chemosensory Dysfunctions After COVID-1911
Using Photographs to Understand the Context of Health: A Novel Two-Step Systematic Process for Coding Visual Data11
Using Online Photovoice to Explore Food Decisions of Families on Low Income: Lessons Learnt During the COVID-19 Pandemic11
“If You Look Closely, You Have Everything …”: Ideas of a Good Life Among Middle-Aged Individuals With Heart Disease: An Interpretative Phenomenological Analysis11
Fraudulent Participation in Online Qualitative Studies: Practical Recommendations on an Emerging Phenomenon11
“There Are Many of Us”: Online Testimonies From “Pill Victims” as a New Form of Health Activism11
Maintaining the Integrity of Qualitatively Driven Mixed Methods: Avoiding the “This Work Is Part of a Larger Study” Syndrome11
Family Caregivers’ Trajectories of Distress While Caring for a Person With Serious Mental Illness11
Supporting Individuals With an Acquired Brain Injury: An Interpretative Phenomenological Study Exploring the Everyday Lives of Caregivers10
Photovoice Revisited: Dialogue and Action as Pivotal10
“The Drug Use Unfortunately isn’t all Bad”: Chronic Disease Self-Management Complexity and Strategy Among Marginalized People Who Use Drugs10
Mechanism-Based Middle-Range Theories: Using Realist Syntheses to Reconcile Specificity to Context and Generalizability10
Exploring Indigenous Ways of Coping After a Wildfire Disaster in Northern Alberta, Canada10
Coalescing, Cross-Pollinating, Crystalising: Developing and Evaluating an Art Installation About Health Knowledge10
The “Sticky Notes” Method: Adapting Interpretive Description Methodology for Team-Based Qualitative Analysis in Community-Based Participatory Research10
Physiotherapists’ Approaches to Patients’ Concerns in Back Pain Consultations Following a Psychologically Informed Training Program10
Confronting the Complexities of “Co-Production” in Participatory Health Research: A Critical, Reflexive Approach to Power Dynamics in a Collaborative Project on Parkinson’s Dance10
“If You Can Just Break the Stigma Around It”: LGBTQI+ Migrants’ Experiences of Stigma and Mental Health10
Prompts, Pearls, Imperfections: Comparing ChatGPT and a Human Researcher in Qualitative Data Analysis10
How and Why Do Multimorbid Patients Decide to Follow Their Multiple Medication Prescriptions? Looking Beyond the Risk–Benefit Scale10
Physician Experiences and Perceived Barriers to Providing Quality Infertility Care in the Greater Accra Region of Ghana9
The Consequences of Female Genital Mutilation on Psycho-Social Well-Being: A Systematic Review of Qualitative Research9
Using Black Feminist Theory and Methods to Uncover Best Practices in Health Promotion Programming9
Aboriginal and Queer Identity/ies in Western Australia: When There is a Need to Know in Therapeutic Settings9
Navigating the Digital Divide: Utilization of Patient Portals Among Older Adults During the COVID-19 Pandemic in the United States9
Qualitative Findings on the Impact of COVID-19 Restrictions on Australian Gay and Bisexual Men: Community Belonging and Mental Well-being9
“You Are Always at War With Yourself” The Perceptions and Beliefs of People With Obesity Regarding Obesity as a Disease9
“I Want to Do Something” – Exploring What Makes Activities Meaningful for Community-Dwelling People Living With Dementia: A Focused Ethnographic Study9
Practitioner Experiences Responding to Suicide Risk for Survivors of Human Trafficking in the Philippines9
Uncovering the Meaning of Parent–Nurse Relationships in Childhood Cancer Care: A Gadamerian Hermeneutic Study9
A Review on Carspecken’s Critical Ethnography9
Recommendations for Virtual Qualitative Health Research During a Pandemic9
Assessing the Effects of Home-Based Primary Care on Alzheimer’s Caregivers and Support Organizations: An Application of the Health Equity Implementation Framework9
Bounded Solidarity as an Asset for Public Health Care Intervention8
Announcing the Agar and Charmaz Awards for 20238
HIV-Related Stigma Among Youth Living With HIV in Western Uganda8
Legislatively Excluded, Medically Uninsured and Structurally Violated: The Social Organization of HIV Healthcare for African, Caribbean and Black Immigrants with Precarious Immigration Status in Toron8
Community Perspectives on Social Influences on Suicide Within a Native American Reservation8
Treatment Burden and Uncertainty in the Context of Advanced Multimorbidity: A Focussed Ethnography8
Self-Management in Older Pakistanis Living With Multimorbidity in East London8
Control Measures for Continuous Deep Sedation Until Death: A Framing Analysis of the Views of Physicians8
Conceptualizing Symptom Invalidation as Experienced by Patients With Endometriosis8
Canadian Men’s Intimate Partner Relationship Break-Ups During COVID-19: Implications for Mental Health Promotion8
A Qualitative Serial Analysis of Drawings by Thirteen-to Fifteen-Year-Old Adolescents in Sweden About the First Wave of the Covid-19 Pandemic8
Trans Youth Talk Back: A Foucauldian Discourse Analysis of Transgender Minors’ Accounts of Healthcare Access7
The Development of Elder-Governed Adjuvant Cultural Therapy for Aboriginal and/or Torres Strait Islander Young People With Mental Health Conditions7
Public Opinion Through Art: Exploring Chinese University Students’ Perspectives on COVID-19 Mass Nucleic Acid Testing7
Barriers to Childhood Immunization in Rural and Remote Areas: A Qualitative Exploration From the Perspectives of Community Leaders in Sindh, Pakistan7
Outsourcing Transcription: Extending Ethical Considerations in Qualitative Research7
‘I Have to Explain to him’: How Companions Broker Mutual Understanding Between Patients with Intellectual Disabilities and Health Care Practitioners in Primary Care7
Personal Agency and Community Resilience: Narratives of Women Navigating Health Care With Chronic Lyme Disease7
A Better Me? An Interpretative Phenomenological Analysis of the Experiences of Female Cancer Survivors’ Heightened Preoccupation With ‘Healthy Eating’7
A Meta-Ethnography on the Impact of Cancer for Lesbian and Queer Women and Their Partners7
‘Make Them Wonder How You Are Still Smiling’: The Lived Experience of Coping With a Brain Tumour7
Engaging the Community in Designing a Hepatitis C Virus Treatment Program for Adults Experiencing Homelessness7
‘A Story of Being Invisible’: A Single Case Study on the Significance of Being Recognised When Needing Acute Healthcare in the Early COVID-19 Pandemic7
Intersectoral Collaboration to Promote Child Development: The Contributions of the Actor-Network Theory7
Long-Acting Injectable Pre-Exposure Prophylaxis Perceptions and Preferences Among Transgender and Nonbinary Young Adults in the United States7
The Phenomenology of the Body After 85 Years7
Constructing a Conformer–Explorer Identity in Pandemic Narratives: A Qualitative Study of Chinese Emerging Adults7
Significance of an Interprofessional Healthy Aging Program for Community-Dwelling Older Adults: A Narrative Study7
Attuning to the World of Peace of Mind and Trust: Women’s Lived Experience of the Woman–Midwife Relationship in Japan7
“100 Things I Wish Someone Would Have Told Me”: Everyday Challenges Parents Face While Caring for Their Children With a Tracheostomy7
Photos Sculpt the Stories of Youth: Using Photovoice to Holistically Capture the Lived Experiences and Pain of Youth Who Underwent Spinal Fusion Surgery7
“You’re Not Alone”: How Adolescents Share Dysmenorrhea Experiences Through Vlogs7
How Culture Shapes Informal Caregiver Motivations: A Meta-Ethnographic Review7
Group Level Assessment Methodology as a Liberating Structure Within Qualitative and Participatory Research7
Relatives’ Experiences of Being Involved in Assisted Dying: A Qualitative Study7
Family Member Experiences in Intensive Care Units Care: Insights From a Family Involvement Tool Implementation Trial7
Reconstructing a Meaningful Self: The Identity Work of People Living With Chronic Disease7
Continuity of Care Advocate Model (CCAM): Healthcare Workers’ Perspectives on Quality Stroke Care at an Acute Unit, Rehabilitation Center and Community Rehabilitation Program in Singapore7
Correction Notice to Family Planning Knowledge, Attitudes, and Practices Among Somali and Congolese Refugee Women after Resettlement to the United States7
How People With Lived Experiences of Homelessness and Sex Trades Become Social Service Leaders in Sex Trafficking, Sex Trading, and Youth Organizations: A Community-Engaged Study7
A Moment of Silence: Pertti (Bert) J. Pelto, July 16, 1927–July 16, 20247
Emotional Labor in Dementia Research6
The Meaning Given to Bioethics as a Source of Support by Physicians Who Care for Children Who Require Long-Term Ventilation6
Life-Course Marginalities of Positive Health and Aging: A Participatory Approach Integrating the Lived Experiences of Older Irish Travelers and Older Homeless Adults in Multistakeholder Research Proce6
Understanding the Narratives of Child Sexual Abuse6
“Not Only a Matter of Personal Interest”—Vaccination Narratives and the Model of Moral Motives in China and Germany6
“Through the Excuse of Football, We Strengthen Medical Services”: How Football-Oriented Sport for Development Organizations Prevent Youth Violence by Promoting Healthy Development in Colombia6
What Does ChatGPT Mean for Qualitative Health Research?6
“The System Tends to Scoop You Up and Spit You Out and They’re Done With You”: The Intersection of Intellectual/Developmental Disability and Homelessness From the Perspectives of Service Providers6
“There’s Something to Remind You that Everything Is Okay”: Australian Trans Young People and the Presence of Animals in Interactions With Healthcare Professionals6
The Experiences, Needs, and Solutions of Caregivers of Patients With Behavioral and Psychological Symptoms of Dementia Living in Residential and Long-Term Care Centers6
Factors Shaping the Implementation of Strategies to Prevent Acute Kidney Injury: A Qualitative Study6
Understanding the Process of Drug Addiction Recovery Through First-Hand Experiences: A Qualitative Study in the Netherlands Using Lifeline Interviews6
Stakeholder Perspectives on Retention Strategies for Rehabilitation Professionals: A Qualitative Study6
“I Will Die by My Own Hand”: Understanding the Development of Suicide Capability in the Narratives of Individuals Who Have Attempted Suicide6
Mapping MAiD Discordance: A Qualitative Analysis of the Factors Complicating MAiD Bereavement in Canada6
Implications of COVID-19 on the Loneliness of Older Adults in Residential Care Homes6
Team-Based Qualitative Rapid Analysis: Approach and Considerations for Conducting Developmental Formative Evaluation for Intervention Design6
Stories of Hope: Young People’s Personal Narratives About ADHD Put Into Context of Positive Aspects6
‘Torn in two’: Experiences of Mothers Who Are Pregnant when Their Child Is Diagnosed With Cancer6
Home as a Place of Refuge, Despair, and Self-Care for Men Living With Mental Health Challenges6
Exploring HIV-Associated Neurocognitive Impairment in the Era of Effective Antiretroviral Therapy: A Primary Healthcare Perspective6
The Unexpected Benefits of a Decolonized Knowledge Translation Initiative for Indigenous Mother Participants6
The Process Model of Stigmatized Loss: Identity-Threatened Experiences of Bereaved Mothers5
Caught on the Fringes of Life: Mothers’ Lived Experiences of Initial Breastfeeding Complications5
Making Sense of Burnout: A Reflexive Thematic Analysis of How Teachers in England Discuss and Encounter the Term Burnout5
The Experience of Phenylketonuria in Pregnancy and the Developing Maternal–Infant Relationship: A Qualitative Study5
The Morality of Care: Female Family Caregivers’ Motivations for Providing Care to Older Migrants5
“You’re Just Stuck in a Hole, Really”: Mechanisms of Structural Racism Through Migrant Agricultural Worker Housing in Canada5
“Your Body Is Not At All Where You Left It”: Adolescent and Young Adult Cancer Survivors’ Experiences Transitioning Back Into Physical Activity After Treatment5
The Changing Care of Older Adults With Bipolar Disorder: A Narrative Analysis5
“You Don’t Realize What a Big Change It Is”: A Reflexive Thematic Analysis of Patients’ Experiences of Amputation Preparation, Information Provision, and Support5
Empowering Cancer Survivors in Managing Their Own Health: A Paradoxical Dynamic Process of Taking and Letting Go of Control5
Video Conferencing Peer Support and Rarer Forms of Dementia: An Exploration of Family Carers’ Positive Experiences5
“There’s So Much More Support We Could Have Provided”: Child Life Specialists’ Stories of the Challenges Working in Adult Oncology5
The Gendered Work/Role of Program Directors in International Graduate Medical Education5
What Makes Intentional Unidirectional Peer Support for Homeless People Work? An Exploratory Analysis Based on Clients’ and Peer Workers’ Perceptions5
A Lasting Impression: Exploring the Meaningfulness of a Singular Moment5
Conversations About Opioids: Impact of the Opioid Overdose Epidemic on Social Interactions for People Who Live With Chronic Pain5
Exploring Journey Maps as Products From Qualitative Research: Application Through Food Insecure Veterans’ Experiences5
The Research Relationship: Negotiating Multiple Selves and Boundaries in Exploring Sensitive Topics5
Gossip and Addiction Recovery in Rural Communities5
“I Get It, I’m Sick Too”: An Autoethnographic Study of One Researcher/Practitioner/Patient With Chronic Illness5
Playing With Peers: Exploring Peer Support Mechanisms of a Type 2 Diabetes-Specific Board Game5
Dignity in Action in the Home Hospice: The Narrative Selection of a Multidisciplinary Staff5
Participatory Action Research and Knowledge Dissemination in Virtual Photovoice: Methodological Insights5
Shadowing Stroke Patients to Explore the Rehabilitation Built Environment: Approach, Insights, and Lessons Learned5
Knowledge and Power Relations in Older Patients’ Communication About Medications Across Transitions of Care5
Collaborative Autoethnography of Cancer Patients’ Dynamic Sense of Agency5
Incongruent Expectations: A Qualitative Study of the Gendered Experiences of Canadian Young People5
‘You Are Not Alone, We’ve Got You’: Power Plays, Devotion, and Punishment on Healthy Eating and Pro-Eating Disorder Websites5
“What other choices might I have made?”: Sexual Minority Men, the PrEP Cascade and the Shifting Subjective Dimensions of HIV Risk5
Community Caring for a Family Member With Brain Injury: Women’s Lived Experiences5
DeusEx Saved My Life: A Feminist-Autoethnography of Video-Gaming Through Major Depressive Disorder5
“We Want parkrun to Well Outlive Us”: Behind the Dissemination and Sustainability of parkrun in Australia4
Transitions Theatre: Creating a Research-Based Reader’s Theatre With Disabled Youth and Their Families4
Collusion in the Clinic: Constructing Patients’ Moral Responsibility to Treat Cancer4
The Adolescent Concept of Social Participation—A Qualitative Study on the Concept of Social Participation from Adolescents with and without Physical Disabilities4
Nature-Based Group Exercises for People With Arthritis: A Qualitative Along-Side Interview Study of Lived Experiences4
Experiences of Conducting Research With Vulnerable and Disempowered Participants in a Developing Country: Perspectives From a Novice Researcher4
Clinician–Patient Relationships in Virtual Care: A Dimensional Analysis of the Symbolic World of Cancer Care4
Caregiver Support in Mental Health Recovery: A Critical Realist Qualitative Research4
Indigenous Women’s Resistance of Colonial Policies, Practices, and Reproductive Coercion4
The Experts’ Advice: Prevention and Responsibility in German Media and Scientific Discourses on Dementia4
Cisheteronormativity, Conversion Therapy, and Identity Among Sexual and Gender Minority People: A Narrative Inquiry and Creative Non-fiction4
“Connection to Culture Is Like a Massive Lifeline”: Yarning With Aboriginal Young People About Culture and Social and Emotional Wellbeing4
“Without IPS I Think I Would Really Fall Apart”: Individual Placement and Support as Experienced by People With Mental Illness—Phenomenological Peer Research Study4
Unvaxxed: A Cultural Study of the Online Anti-Vaccination Movement4
Customizing Health Recommendations About Physical Activity During Pregnancy: A Qualitative Study Among Practitioners in France4
Doctors, Patients, and Interpreters’ Views on the Co-Construction of Empathic Communication in Interpreter-Mediated Consultations: A Qualitative Content Analysis of Video Stimulated Recall Interviews4
Where’s the Disconnect? Exploring Pathways to Healthcare Coordinated for Youth Experiencing Homelessness in Toronto, Canada, Using Grounded Theory Methodology4
Exploring Cancer Pain Self-Management Needs and Preferences: A Meta-Ethnography4
“I’m Fighting for My Life”: Exploring Interactions Between Black Women with Breast Cancer and Healthcare Providers4
American Indian Behavioral Health Treatment Preferences as Perceived by Urban Indian Health Program Providers4
Healthcare Barriers Among Working-Age Persons with Disabilities in Trinidad4
We Speak a Different Language: End-of-Life and Bereavement Experiences of Older Lesbian, Gay, and Bisexual Women Who Have Lost a Spouse or Partner4
Engaging in Palliative Care Conversations With Healthcare Providers: A Phenomenological Young Adult Cancer Study4
Managing Uncertainty for and With Family: Communication Strategies and Motivations in Familial Uncertainty Management for Hereditary Cancer4
Erratum to ‘We Ought to Be Professionals’: Strategies of Intrapersonal and Interpersonal Emotion Regulation of Emergency Medical Services Professionals in Confrontation With the Death of a Newborn in 4
Understanding Gut Feelings: Transformations in Coping With Inflammatory Bowel Disease Among Young Adults4
Recruiting a Hard-to-Reach, Hidden and Vulnerable Population: The Methodological and Practical Pitfalls of Researching Vaccine-Hesitant Parents4
Integrating Traditional Medicine and Healing into the Ghanaian Mainstream Health System: Voices From Within4
Connecting Through Dance: Understanding Conscious Clubbing Event Experiences4
Improving Collaboration Between Staff, Family Members, and Artists in Long-Term Dementia Care: A Participatory Action Research Project Into Health Care Clowning4
Perceptions and Attitudes Toward Genetic Counselors and Genetic Testing Among Certified Professional Midwives in Vermont: A Modified Grounded Theory Study4
Thank You to Our Reviewers4
Analysis and Interpretation of Metaphors: Exploring Young Adults’ Subjective Experiences With Depression4
Doing Phenomenological Research and Writing4
Empathic Validation in Physician–Patient Communication: An Approach to Conveying Empathy for Problems With Uncertain Solutions4
Reproduction and Genetic Responsibility: An Interpretive Description of Reproductive Decision-Making for Young People With Li-Fraumeni Syndrome4
And It’ll Come Back Real Baby Fine: Black Women’s Experiences With Hair Loss and Regrowth After Chemotherapy for Breast Cancer Treatment4
Grandfathers’ Experiences of Grief and Support Following Pregnancy Loss or Neonatal Death of a Grandchild4
Understanding Causation in Healthcare: An Introduction to Critical Realism4
Observation and Institutional Ethnography: Helping Us to See Better4
“They Didn’t Ask.” Rural Women With Disabilities and Experiences of Violence Describe Interactions With the Healthcare System4
Key Informants in Applied Qualitative Health Research4
A Closer Look: Examining Cultural–Contextual Influences on Weight Management Through Focus Groups With Church-Going African American Women4
Coping With a Dead End by Relying on Your Own Compass: A Qualitative Study on Illness and Treatment Models in the Context of Fibromyalgia4
The Surgical Sisterhood – The Experiences of wāhine Māori and Pasifika Aspiring Surgeons3
Embodying the (Dis)embodiment: Narrating Depersonalization-Derealization Disorder3
Bound in an Imbalanced Relationship: Family Caregivers and Migrant Live-In Care-Workers of Frail Older Persons in Israel3
Understanding the Experiences of COVID-19 Public Health Measures and Well-Being: A Qualitative Study Among Older Adults in Quebec, Canada3
Exploring the Methodological Benefits and Challenges of Utilising a Photovoice Methodology With Individuals in Recovery From Problem Substance Use3
Who’s Involved? Case Reports on Older Adults’ Alcohol and Tobacco Use in Dutch Residential Care Facilities3
How Community-Based Health and Social Care Professionals Support Unpaid Caregivers: Experiences From One Health Authority in Ontario, Canada3
Experience of Transitional Care Among Thai-Isan Older Stroke Survivors and Their Family Caregivers3
How Do University Students Navigate Distress? An Examination of Determinants, Coping Strategies, and Support Systems Through the Lens of Self-Determination Theory3
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