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 2020-04-01 to 2024-04-01.)
ArticleCitations
Carrying Out Rapid Qualitative Research During a Pandemic: Emerging Lessons From COVID-19280
Rapid Techniques in Qualitative Research: A Critical Review of the Literature174
Face-to-Face Compared With Online Collected Accounts of Health and Illness Experiences: A Scoping Review76
Recommendations for Virtual Qualitative Health Research During a Pandemic58
The Factors That Promote Vaccine Hesitancy, Rejection, or Delay in Parents58
Collective Emotion During Collective Trauma: A Metaphor Analysis of the COVID-19 Pandemic52
Racism in European Health Care: Structural Violence and Beyond50
Former NICU Families Describe Gaps in Family-Centered Care49
How Participatory Music Engagement Supports Mental Well-being: A Meta-Ethnography35
“When Is Health Care Actually Going to Be Care?” The Lived Experience of Family Planning Care Among Young Black Women32
“They’re Not Willing To Accommodate Deaf patients”: Communication Experiences of Deaf American Sign Language Users in the Emergency Department31
Complex Qualitative Data Analysis: Lessons Learned From the Experiences With the Qualitative Analysis Guide of Leuven29
Alone in a Time of Pandemic: Solo-Living Women Coping With Physical Isolation29
Intersectionality of Resilience: A Strengths-Based Case Study Approach With Indigenous Youth in an Urban Canadian Context28
Gratitude in Health Care: A Meta-narrative Review28
Examining What We Know in Relation to How We Know It: A Team-Based Reflexivity Model for Rapid Qualitative Health Research28
The Social Ecology of Power in Participatory Health Research28
Chinese Migrant Workers’ Care Experiences: A Model of the Mediating Roles of Filial Piety28
It’s Not Just a Virus! Lived Experiences of People Diagnosed With COVID-19 Infection in Denmark27
Overcoming Barriers: Individual Experiences Obtaining Medication-Assisted Treatment for Opioid Use Disorder26
“He’s Back so I’m Not Alone”: The Impact of Deep Brain Stimulation on Personality, Self, and Relationships in Parkinson’s Disease26
Doing Phenomenological Research and Writing26
The Consequences of Female Genital Mutilation on Psycho-Social Well-Being: A Systematic Review of Qualitative Research26
Antimicrobial Resistance, Politics, and Practice in India25
The Diagnostic Experiences of Women With Polycystic Ovary Syndrome (PCOS) in Ontario, Canada22
Conceptualizing Qualitative Data22
“It Went to the Very Heart of Who I Was as a Woman”: The Invisible Impacts of Intimate Partner Sexual Violence21
Sex: What Is the Big Deal? Exploring Individuals’ with Intellectual Disabilities Experiences with Sex Education21
Qualitative Findings on the Impact of COVID-19 Restrictions on Australian Gay and Bisexual Men: Community Belonging and Mental Well-being21
Implications of COVID-19 on the Loneliness of Older Adults in Residential Care Homes21
“Connection to Culture Is Like a Massive Lifeline”: Yarning With Aboriginal Young People About Culture and Social and Emotional Wellbeing20
“Why Am I Not Taking Medications?” Barriers and Facilitators of Diabetes Medication Adherence Across Different Health Literacy Levels20
Use of the Patient Health Questionnaire (PHQ-9) in Practice: Interactions between patients and physicians20
Body Image and Eating Disorders Among South Asian American Women: What Are We Missing?20
“I Can Understand Where They’re Coming From”: How Clinicians’ Disability Experiences Shape Their Interaction With Clients19
Confronting the Complexities of “Co-Production” in Participatory Health Research: A Critical, Reflexive Approach to Power Dynamics in a Collaborative Project on Parkinson’s Dance19
Health Care Professionals’ and Patients’ Management of the Interactional Practices in Telemedicine Videoconferencing: A Conversation Analytic and Discursive Systematic Review19
Availability, Accessibility, Acceptability, and Quality of Interpreting Services to Refugee Women in New Zealand18
Digital Storytelling as a Patient Engagement and Research Approach With First Nations Women: How the Medicine Wheel Guided Our Debwewin Journey18
Using the Framework Method for the Analysis of Qualitative Dyadic Data in Health Research18
First-Time Mothers’ Expectations and Experiences of Postnatal Care in England17
It’s in Me to Give: Canadian Gay, Bisexual, and Queer Men’s Willingness to Donate Blood If Eligible Despite Feelings of Policy Discrimination17
Conversations About Opioids: Impact of the Opioid Overdose Epidemic on Social Interactions for People Who Live With Chronic Pain17
Working with Aboriginal young people in sexual health research: a peer research methodology in remote Australia17
Supporting Vulnerable Populations During the Pandemic: Stakeholders’ Experiences and Perceptions of Social Prescribing in Scotland During Covid-1916
Physiotherapists Both Reproduce and Resist Biomedical Dominance when Working With People With Low Back Pain: A Qualitative Study Towards New Praxis16
Family Sense-Making After a Down Syndrome Diagnosis16
“What Is Right for Me, Is Not Necessarily Right for You”: The Endogenous Factors Influencing Nonparticipation in Medical Assistance in Dying16
Patients’ Experiences of Comorbid HIV/AIDS and Diabetes Care and Management in Soweto, South Africa15
Falling Down the Rabbit Hole: Child and Family Experiences of Pediatric Hematopoietic Stem Cell Transplant15
Understanding the Role of Past Health Care Discrimination in Help-Seeking and Shared Decision-Making for Depression Treatment Preferences15
Empowering People to Make Healthier Choices: A Critical Discourse Analysis of the Tackling Obesity Policy15
“I Was Raised in Addiction”: Constructions of the Self and the Other in Discourses of Addiction and Recovery15
Access to Psychological Support for Young People Following Stoma Surgery: Exploring Patients’ and Clinicians’ Perspectives14
Caregiver Support in Mental Health Recovery: A Critical Realist Qualitative Research14
Sick of the Sick Role: Narratives of What “Recovery” Means to People With CFS/ME14
A Critical Perspective on Mental Health News in Six European Countries: How Are “Mental Health/Illness” and “Mental Health Literacy” Rhetorically Constructed?14
“I Am Okay With It, But I Am Not Going to Do It”: The Exogenous Factors Influencing Non-Participation in Medical Assistance in Dying14
Unvaxxed: A Cultural Study of the Online Anti-Vaccination Movement14
“An Active, Productive Life”: Narratives of, and Through, Participation in Public and Patient Involvement in Health Research14
Older Adults’ Narratives of Seeking Mental Health Treatment: Making Sense of Mental Health Challenges and “Muddling Through” to Care14
Integrating Traditional Medicine and Healing into the Ghanaian Mainstream Health System: Voices From Within14
Physiotherapists’ Approaches to Patients’ Concerns in Back Pain Consultations Following a Psychologically Informed Training Program13
What Moves People Living With Dementia? Exploring Barriers and Motivators for Physical Activity Perceived by People Living With Dementia in Care Homes13
Managing Uncertainty During the Communication of Diagnostic Test Information Between Patients and Clinicians in Australian Emergency Care13
“Having a Baby Can Wait”: Experiences of a Sexual and Reproductive Health Promotion Program in the Context of Homelessness among Asian American, Native Hawaiian, and Other Pacific Islander Youth Captu13
Decisions and Dilemmas: The Context of Prioritization Dilemmas and Influences on Staff Members’ Prioritization Decisions in Residential Aged Care13
Simulation-Based Research: A Scoping Review13
Moving Beyond Text-and-Talk in Qualitative Health Research: Methodological Considerations of Using Multiple Media for Data Collection12
“There Is So Much More for Us to Lose If We Were to Kill Ourselves”: Understanding Paradoxically Low Rates of Self-Harm in a Socioeconomically Disadvantaged Community in London12
Qualitative Research and Its Importance in Adapting Interventions12
Designing an “Ideal” Substance Use Disorder Treatment Center: Perspectives of People Who Have Utilized Medications for Opioid Use Disorder12
“What Will Come Will Come”: The Journey of Adjustment and Acceptance on the Path of Dementia Care Among Vietnamese Family Caregivers12
“I Will Not Be Defined by This. I’m Not Going to Live Like a Victim; It Is Not Going to Define My Life”: Exploring Breast Cancer Survivors’ Experiences and Sense of Self12
“Now I Am Myself”: Exploring How People With Poststroke Aphasia Experienced Solution-Focused Brief Therapy Within the SOFIA Trial12
Qualitative Data Sharing: Participant Understanding, Motivation, and Consent12
Collaborative Filmmaking: A Participatory, Visual Research Method12
Health Care Providers’ Challenges to High-Quality HIV Care and Antiretroviral Treatment Retention in Rural South Africa12
“Body as a Machine”: How Adolescents With Sickle Cell Disease Construct Their Fatigue Experiences11
The Experiences of People Living With Chronic Pain During a Pandemic: “Crumbling Dreams With Uncertain Futures”11
“But I Gathered My Courage”: HIV Self-Testing as a Pathway of Empowerment Among Ugandan Female Sex Workers11
Age, Dementia, and Diagnostic Candidacy: Examining the Diagnosis of Young Onset Dementia Using the Candidacy Framework11
Experiences of Pain in Hospitalized Children During Hematopoietic Stem Cell Transplantation Therapy11
The Other Side of Through: Young Breast Cancer Survivors’ Spectrum of Sexual and Reproductive Health Needs11
The Social Construction of a Concept—Orthorexia Nervosa: Morality Narratives and Psycho-Politics11
Negotiating Female Genital Cutting in a Transnational Context11
Why the Qualitative Health Research (QHR) Review Process Does Not Use Checklists11
The “Sticky Notes” Method: Adapting Interpretive Description Methodology for Team-Based Qualitative Analysis in Community-Based Participatory Research11
“Painful, yet Beautiful, Moments”: Pathways Through Infant Feeding and Dynamic Conceptions of Breastfeeding Success11
Black Women’s Lived Experiences of Abortion11
We Need to Talk About Complexity in Health Research: Findings From a Focused Ethnography11
Fierce Autonomy: How Girls and Young Women Impacted by Commercial Sexual Exploitation Perceive Health and Exercise Agency in Health Care Decision-Making11
Co-designing an Integrated Care Network With People Living With Parkinson’s Disease: From Patients’ Narratives to Trajectory Analysis10
Qualitative Methods in Health Policy and Systems Research: A Framework for Study Planning10
“The Drug Use Unfortunately isn’t all Bad”: Chronic Disease Self-Management Complexity and Strategy Among Marginalized People Who Use Drugs10
How to Save a Life: Vital Clues From Men Who Have Attempted Suicide10
Harm Reduction for Women in Treatment for Alcohol Use Problems: Exploring the Impact of Dominant Addiction Discourse10
“I Feel Abused by My Own Mind”: Themes of Control in Men’s Online Accounts of Living With Anxiety10
Parental Perspectives on Family Mealtimes Related to Gastrostomy Tube Feeding in Children10
The Experts’ Advice: Prevention and Responsibility in German Media and Scientific Discourses on Dementia10
Sexual and Reproductive Health Information and Experiences Among Syrian Refugee Adolescent Girls in Lebanon10
How do Healthcare Workers ‘Do’ Guidelines? Exploring How Policy Decisions Impacted UK Healthcare Workers During the First Phase of the COVID-19 Pandemic9
I Tried Forcing Myself to do It, but Then It Becomes a Boring Chore”: Understanding (dis)engagement in Physical Activity Among Individuals With Type 2 Diabetes Using a Practice Theory Approach9
(Mis)recognition in the Therapeutic Alliance: The Experience of Mental Health Interpreters Working With Refugees in U.K. Clinical Settings9
“Why Would I Talk To Them About Sex?”: Exploring Patient-Provider Communication Among Black Women Experiencing Sexual Pain9
Navigating Intersectional Stigma: Strategies for Coping Among Cisgender Women of Color9
The Parental Struggle With the Israeli Genital Socialization Process9
From Danger to Uncertainty: Changing Health Care Practices, Everyday Experiences, and Temporalities in Dealing With COVID-19 Policies in the Netherlands9
The Balance of Patient Involvement: Patients’ and Health Professionals’ Perspectives on Decision-Making in the Treatment of Advanced Prostate Cancer9
Stumbling Into Adulthood: Learning From Depression While Growing Up9
Motivations for PrEP-Related Interpersonal Communication Among Women Who Inject Drugs: A Qualitative Egocentric Network Study9
“We All Join Hands”: Perceptions of the Kangaroo Method Among Female Relatives of Newborns in The Gambia9
Feelings, Thoughts, and Behaviors During Disaster9
The Changing Narratives of Death, Dying, and HIV in the United Kingdom9
Understanding the Lived Experience of Children With Type 1 Diabetes in Kenya: Daily Routines and Adaptation Over Time9
Organ Transplant Recipients’ Experiences of Physical Activity: Health, Self-Care, and Transliminality9
Yarning as an Interview Method for Non-Indigenous Clinicians and Health Researchers9
A Constructed Reality? A Fairclough-Inspired Critical Discourse Analysis of the Danish HPV Controversy9
Photovoice Revisited: Dialogue and Action as Pivotal9
Dignity as an Intersubjective Phenomenon: Experiences of Dyads Living With Serious Illness9
Acceptance of the HPV Vaccine in a Multiethnic Sample of Latinx Mothers8
“Love Can’t Be Taken to the Hospital. If It Were Possible, It Would Be Better”: Patients’ Experiences of Being Cared for in an Intensive Care Unit8
Modes of Interaction in Naturally Occurring Medical Encounters With General Practitioners: The “One in a Million” Study8
Cultural Bereavement and Resilience in Refugee Resettlement: A Photovoice Study With Yazidi Women in the Midwest United States8
Socially Constructing Healthy Eating: A Foucauldian Discourse Analysis of Healthy Eating Information and Advice8
From Theory to Implementation: Adaptations to a Quality Improvement Initiative According to Implementation Context8
“You Are By No Means Alone”: A Netnographic Study of Self-Care Support in an Online Community for Older Adults8
The Impact of Binational Barriers to Medical Care on the Care-Seeking Practices of Mexican Immigrants8
“What other choices might I have made?”: Sexual Minority Men, the PrEP Cascade and the Shifting Subjective Dimensions of HIV Risk8
Minding the Gap Between the Policy and Practice of Patient-Centeredness: Cocreating a Model for Tensional Dialogue in the “Active Patient Support” Program8
Not Enough Money and Too Many Thoughts: Exploring Perceptions of Mental Health in Two Ugandan Districts Through the Mental Health Literacy Framework8
Experiences of Tourette Syndrome Caregivers With Supportive Communication8
Surprise Reveals the Affective-Moral Economies in Cancer Illness Narratives8
Diabetes Identity: A Mechanism of Social Change8
Adherence and the Moral Construction of the Self: A Narrative Analysis of Anticoagulant Medication8
Contributions of Preventive Social Services in Early Childhood Home Visiting in a Disadvantaged Area of Sweden: The Practice of the Parental Advisor8
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 People8
The “Be All and End All”? Young People, Online Sexual Health Information, Science and Skepticism8
U.S. Abortion Care Providers’ Perspectives on Self-Managed Abortion8
‘The System is Not Set up for the Benefit of Women’: Women’s Experiences of Decision-Making During Pregnancy and Birth in Ireland8
“Making a Way Out of No Way:” Understanding the Sexual and Reproductive Health Care Experiences of Transmasculine Young Adults of Color in the United States8
Understanding the Course of Critical Illness Through a Lifeworld Approach7
“It’s a Bit of a Double-Edged Sword”: Motivation and Personal Impact of Bereaved Mothers’ Advocacy for Drug Policy Reform7
Cancer-Related Decision-Making Among Adolescents, Young Adults, Caregivers, and Oncology Providers7
Emerging From the “Ku:” Fluctuating in Adjusting With Breast Cancer—A Post-Traumatic Growth Theory Situated Within Chinese Culture7
Living With Fear: Experiences of Danish Parents in Vulnerable Positions During Pregnancy and in the Postnatal Period7
Trans Youth Talk Back: A Foucauldian Discourse Analysis of Transgender Minors’ Accounts of Healthcare Access7
Using Black Feminist Theory and Methods to Uncover Best Practices in Health Promotion Programming7
Making Public Involvement in Research More Inclusive of People With Complex Speech and Motor Disorders: The I-ASC Project7
Grassroots Mental Health Groups’ Use of Advocacy Strategies in Social Media Messaging7
The Emotional and Psychological Labor of Insider Qualitative Research Among Systemically Marginalized Groups: Revisiting the Uses of Reflexivity7
Development of PARcific Approach: Participatory Action Research Methodology for Collectivist Health Research7
Reframing How Early Pregnancy Loss Is Viewed in the Emergency Department7
Chronic Illness Management in Culturally and Linguistically Diverse Patients: Exploring the Needs, Access, and Understanding of Information7
The Challenges of Conducting Qualitative Research on “couples” in Abusive Intimate Partner Relationships Involving Substance Use7
Dialoguing With Images: An Expressive Arts Method for Health Research7
Successfully Negotiating Life Challenges: Learnings From Adults With Cerebral Palsy7
Observation and Institutional Ethnography: Helping Us to See Better7
Exploration of Physical Activity Barriers and Facilitators Among Adults in Kathmandu, Nepal7
Community Perspectives on Social Influences on Suicide Within a Native American Reservation7
Treatment Experiences Among People Who Use Opioids: A Social Ecological Approach7
“What I Would Do to Take Away Your Pain”: A Photovoice Project Conducted by Mothers of Children With Medical Complexity7
Evaluating Complex Interventions Using Qualitative Longitudinal Research: A Case Study of Understanding Pathways to Violence Prevention7
Managing Precarity: Understanding Latinas’ Sexual and Reproductive Care-Seeking in a Midwest Emergent Latino Community7
“Did I Choose a Birth Control Method Yet?”: Health Care and Women’s Contraceptive Decision-Making7
Identifying and Responding to Delirium in Acute Stroke: Clinical Team Members’ Understandings7
Experiencing the SARS-CoV-2 Pandemic Whilst Living With Cancer7
Social Processes Informing Toileting Behavior Among Adolescent and Adult Women: Social Cognitive Theory as an Interpretative Lens7
Healthcare Barriers Among Working-Age Persons with Disabilities in Trinidad7
Evaluation of a 20-Month Physical Activity Intervention to Improve Motivational and Affective Outcomes Among Disadvantaged Adult Women7
Ethnography in Health Services Research: Oscillation Between Theory and Practice7
Emotional Health Work of Women With Female Genital Cutting Prior to Reproductive Health Care Encounters7
‘Today Was Probably One of the Most Challenging Workdays I’ve Ever Had’: Doing Remote Qualitative Research with Hospital Doctors During the COVID-19 Pandemic7
The (Co)Production of Difference in the Care of Patients With Cancer From Migrant Backgrounds7
Where Does Value Lie in Peer Support? An Exploratory Discussion of the Theories and Methods Underpinning Effective Research in Peer Support6
“I Look at You and See You Looking at Me”: Role Boundaries in a Dynamic Research Relationship in Qualitative Health Research With Refugees6
A Theory on the Components of Depression Self-Management in Older Adults6
The Meaning Given to Bioethics as a Source of Support by Physicians Who Care for Children Who Require Long-Term Ventilation6
Boundary-Work and the Distribution of Care for Survivors of Domestic Violence and Abuse in Primary Care Settings: Perspectives From U.K. Clinicians6
Comparing Patients’ Experiences in Three Differentiated Service Delivery Models for HIV Treatment in South Africa6
HIV Diagnosis as Both Biographical Disruption and Biographical Reinforcement: Experiences of HIV Diagnoses Among Recently Diagnosed People Living With HIV6
Making Conversation Analysis Accessible: A Conceptual Guide for Health Services Researchers6
“We Are Doing These Things So That People Will Not Laugh at Us”: Caregivers’ Attitudes About Dementia and Caregiving in Nigeria6
“Will You Still Feel Beautiful When You Find Out You Are Different?”: Parents’ Experiences, Reflections, and Appearance-Focused Conversations About Their Child’s Visible Difference6
An Unexpected Journey: The Lived Experiences of Patients with Long-Term Cognitive Sequelae After Recovering from COVID-196
The Cultural and Methodological Factors Challenging the Success of the Community-Based Participatory Research Approach When Designing a Study on Adolescents Sexuality in Traditional Society6
Outsourcing Transcription: Extending Ethical Considerations in Qualitative Research6
A Life Course Perspective on Growing Older With Cerebral Palsy6
Professional Interpreters and Vicarious Trauma: An Australian Perspective6
Water Scarcity and Water Quality: Identifying Potential Unintended Harms and Mitigation Strategies in the Implementation of the Biosand Filter in Rural Tanzania6
Practitioner Experiences Responding to Suicide Risk for Survivors of Human Trafficking in the Philippines6
Moving on From the Delphi Study: The Development of a Physical Activity Training Programme Prototype Through Co-produced Qualitative Research6
A Reflexive Lens on Preparing and Conducting Semi-structured Interviews with Academic Colleagues6
The Intersection of Problems, Policy, and Politics: The Adoption of an HPV Vaccine School-Entry Requirement in Puerto Rico6
Women, Exercise, and Eating Disorder Recovery: The Normal and the Pathological6
Grounded in Culture: Reflections on Sitting Outside the Circle in Community-Based Research With Indigenous Men6
Perspectives and Experiences of Obstetricians Who Provide Labor and Delivery Care for Micronesian Women in Hawai‘i: What Is Driving Cesarean Delivery Rates?6
Speaking Shame and Laughing It Off: Using Humorous Narrative to Conquer the Shame of Anorectal Illness6
How Culture Shapes Informal Caregiver Motivations: A Meta-Ethnographic Review6
Pentadic Cartography: Mapping Postpartum Psychosis Narratives6
Managing Strong Emotions: Nurses’ Recognition and Responses to Personal Emotions When Approaching Parents With Cancer and Their Dependent Children6
Introducing SAMMSA, a Five-Step Method for Producing ‘Quality’ Qualitative Analysis6
Exploring Indigenous Ways of Coping After a Wildfire Disaster in Northern Alberta, Canada6
“Sewing Is Part of Our Tradition”: A Case Study of Sewing as a Strategy for Arts-Based Inquiry in Health Research With Inuit Women6
“Communitas in Crisis”: An Autoethnography of Psychosis Under Lockdown6
Palliative Professionals’ Experiences of Receiving Gratitude: A Transformative and Protective Resource6
Ethics Review Boards for Research With Human Participants: Past, Present, and Future6
Expectations and Concerns of Older Adults With Cognitive Impairment About Their Relationship With Medical Providers: A Call for Therapeutic Alliances5
Telemediated Training in the Home as a Part of the Everyday Life and Practice With Very Severe Chronic Obstructive Pulmonary Disease5
Is a Picture Worth a Thousand Words? Using Photo-Elicitation to Study Body Image in Middle-to-Older Age Women With and Without Multiple Sclerosis5
Benefits and Challenges of Assistance Dogs for Families of Children on the Autism Spectrum: Mothers’ Perspectives5
The Adolescent Concept of Social Participation—A Qualitative Study on the Concept of Social Participation from Adolescents with and without Physical Disabilities5
HIV-Related Stigma Among Youth Living With HIV in Western Uganda5
Indigenous Women’s Resistance of Colonial Policies, Practices, and Reproductive Coercion5
Challenging the Constraints of Neoliberalism and Biomedicalism: Repositioning Social Work in Mental Health5
Photovoice and Instagram as Strategies for Youth Engagement in Disaster Risk Reduction5
Using Linguistic Ethnography to Study Video Consultations: A Call to Action and Future Research Agenda5
“You Could Tell I Said the Wrong Things”: Constructions of Sexual Identity Among Older Gay Men in Healthcare Settings5
PTSD Symptoms and Dementia in Older Veterans Who are Living in Long-Term Care5
‘Whose life are They Going to Save? It’s Probably Not Going to be Mine!’ Living With a Life-Shortening Condition During the Coronavirus (COVID-19) Pandemic: A Grounded Theory Study of Embodied Precari5
“The Food Matches the Mood”: Experiences of Eating Disorders in Bipolar Disorder5
Primary Immunodeficiency Diseases and Gastrointestinal Distress: Coping Strategies and Dietary Experiences to Relieve Symptoms5
The Experiences of Female IBS Patients Concerning Physical Activity as Treatment Modality: A Qualitative Study5
Understanding Gut Feelings: Transformations in Coping With Inflammatory Bowel Disease Among Young Adults5
Understanding Causation in Healthcare: An Introduction to Critical Realism5
Legislatively Excluded, Medically Uninsured and Structurally Violated: The Social Organization of HIV Healthcare for African, Caribbean and Black Immigrants with Precarious Immigration Status in Toron5
‘It’s Not Really a Part of Standard Practice’: Institutional Silencing of Sexuality Within Australian Mental Health Settings5
Identifying “What Matters Most” to Men in Botswana to Promote Resistance to HIV-Related Stigma5
Asian Immigrant Parents’ Role Enactment While Accessing and Using Services for Their Child With Developmental Disabilities in the United States: A Meta-Synthesis Study5
Struggling Together: Examining the Narratives of Interdependence and Healing Within Romantic Relationships After Stroke5
Under- or Overtreatment of Mental Distress? Practices, Consequences, and Resistance in the Field of Mental Health Care5
The Reproductive Health Priorities, Concerns, and Needs of Women in Midlife: A Feminist Poststructuralist Qualitative Analysis5
The Weight of Words: Co-Analysis of Thick Ethnographic Description and “Friction” as Methodological Strategies in a Health Policy Research Partnership5
Counter-Narratives of Structural Oppressions, Stigma and Resistance, and Reproductive and Sexual Health Among Youth Experiencing Homelessness5
Empathic Validation in Physician–Patient Communication: An Approach to Conveying Empathy for Problems With Uncertain Solutions5
“My Whole World Fell Apart”: Parents Discovering Their Child Has Anorexia Nervosa5
They Affect the Person, but for Better or Worse? Perceptions of Electroceutical Interventions for Depression Among Psychiatrists, Patients, and the Public5
“If You Can Just Break the Stigma Around It”: LGBTQI+ Migrants’ Experiences of Stigma and Mental Health5
Sexual Feelings Toward Clients in the Psychotherapeutic Relationship: The Taboo Revealed5
The Wicked Problem of Stigma for Youth Living With Anxiety5
You Have to Pay to Live: Somali Young Adult Experiences With the U.S. Health Care System5
The Phenomenology of the Body After 85 Years4
Social Influences on Engagement With HIV Testing, Treatment and Care Services Among Men Who Have Sex With Men Living in Rural Uganda4
Exploring the Link Between the Hazards and Value of Work, and Overcoming Risk for Community-Based Health Interventions for Immigrant Latinx Low-Wage Workers4
Unsettling Knowledge Synthesis Methods Using Institutional Ethnography: Reflections on the Scoping Review as a Critical Knowledge Synthesis Tool4
“You Probably Won’t Notice Any Symptoms”: Blood Pressure in Pregnancy—Discourses of Contested Expertise in an Era of Self-Care and Responsibilization4
Self-Management in Older Pakistanis Living With Multimorbidity in East London4
Engaging the Community in Designing a Hepatitis C Virus Treatment Program for Adults Experiencing Homelessness4
“You Are Always at War With Yourself” The Perceptions and Beliefs of People With Obesity Regarding Obesity as a Disease4
The Journey of Humanizing Care for People With Disabilities4
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