Qualitative Health Research

Papers
(The TQCC of Qualitative Health Research is 7. 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 2020-05-01 to 2024-05-01.)
ArticleCitations
Carrying Out Rapid Qualitative Research During a Pandemic: Emerging Lessons From COVID-19284
Rapid Techniques in Qualitative Research: A Critical Review of the Literature185
Face-to-Face Compared With Online Collected Accounts of Health and Illness Experiences: A Scoping Review78
Recommendations for Virtual Qualitative Health Research During a Pandemic63
The Factors That Promote Vaccine Hesitancy, Rejection, or Delay in Parents59
Collective Emotion During Collective Trauma: A Metaphor Analysis of the COVID-19 Pandemic53
Racism in European Health Care: Structural Violence and Beyond51
Former NICU Families Describe Gaps in Family-Centered Care50
How Participatory Music Engagement Supports Mental Well-being: A Meta-Ethnography35
The Social Ecology of Power in Participatory Health Research32
“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
Gratitude in Health Care: A Meta-narrative Review30
Intersectionality of Resilience: A Strengths-Based Case Study Approach With Indigenous Youth in an Urban Canadian Context29
Chinese Migrant Workers’ Care Experiences: A Model of the Mediating Roles of Filial Piety29
Alone in a Time of Pandemic: Solo-Living Women Coping With Physical Isolation29
Complex Qualitative Data Analysis: Lessons Learned From the Experiences With the Qualitative Analysis Guide of Leuven29
Examining What We Know in Relation to How We Know It: A Team-Based Reflexivity Model for Rapid Qualitative Health Research29
The Consequences of Female Genital Mutilation on Psycho-Social Well-Being: A Systematic Review of Qualitative Research28
Doing Phenomenological Research and Writing27
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
Antimicrobial Resistance, Politics, and Practice in India25
Conceptualizing Qualitative Data24
“It Went to the Very Heart of Who I Was as a Woman”: The Invisible Impacts of Intimate Partner Sexual Violence24
The Diagnostic Experiences of Women With Polycystic Ovary Syndrome (PCOS) in Ontario, Canada22
Use of the Patient Health Questionnaire (PHQ-9) in Practice: Interactions between patients and physicians22
Using the Framework Method for the Analysis of Qualitative Dyadic Data in Health Research21
Qualitative Findings on the Impact of COVID-19 Restrictions on Australian Gay and Bisexual Men: Community Belonging and Mental Well-being21
“Connection to Culture Is Like a Massive Lifeline”: Yarning With Aboriginal Young People About Culture and Social and Emotional Wellbeing21
Sex: What Is the Big Deal? Exploring Individuals’ with Intellectual Disabilities Experiences with Sex Education21
Implications of COVID-19 on the Loneliness of Older Adults in Residential Care Homes21
Health Care Professionals’ and Patients’ Management of the Interactional Practices in Telemedicine Videoconferencing: A Conversation Analytic and Discursive Systematic Review20
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 Clients20
“Why Am I Not Taking Medications?” Barriers and Facilitators of Diabetes Medication Adherence Across Different Health Literacy Levels20
Digital Storytelling as a Patient Engagement and Research Approach With First Nations Women: How the Medicine Wheel Guided Our Debwewin Journey19
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
Physiotherapists Both Reproduce and Resist Biomedical Dominance when Working With People With Low Back Pain: A Qualitative Study Towards New Praxis18
It’s in Me to Give: Canadian Gay, Bisexual, and Queer Men’s Willingness to Donate Blood If Eligible Despite Feelings of Policy Discrimination18
Availability, Accessibility, Acceptability, and Quality of Interpreting Services to Refugee Women in New Zealand18
First-Time Mothers’ Expectations and Experiences of Postnatal Care in England18
“I Was Raised in Addiction”: Constructions of the Self and the Other in Discourses of Addiction and Recovery17
Family Sense-Making After a Down Syndrome Diagnosis17
“What Is Right for Me, Is Not Necessarily Right for You”: The Endogenous Factors Influencing Nonparticipation in Medical Assistance in Dying17
Working with Aboriginal young people in sexual health research: a peer research methodology in remote Australia17
Conversations About Opioids: Impact of the Opioid Overdose Epidemic on Social Interactions for People Who Live With Chronic Pain17
Integrating Traditional Medicine and Healing into the Ghanaian Mainstream Health System: Voices From Within16
Supporting Vulnerable Populations During the Pandemic: Stakeholders’ Experiences and Perceptions of Social Prescribing in Scotland During Covid-1916
Understanding the Role of Past Health Care Discrimination in Help-Seeking and Shared Decision-Making for Depression Treatment Preferences16
“I Am Okay With It, But I Am Not Going to Do It”: The Exogenous Factors Influencing Non-Participation in Medical Assistance in Dying15
Patients’ Experiences of Comorbid HIV/AIDS and Diabetes Care and Management in Soweto, South Africa15
Older Adults’ Narratives of Seeking Mental Health Treatment: Making Sense of Mental Health Challenges and “Muddling Through” to Care15
Access to Psychological Support for Young People Following Stoma Surgery: Exploring Patients’ and Clinicians’ Perspectives15
Qualitative Research and Its Importance in Adapting Interventions15
What Moves People Living With Dementia? Exploring Barriers and Motivators for Physical Activity Perceived by People Living With Dementia in Care Homes15
Empowering People to Make Healthier Choices: A Critical Discourse Analysis of the Tackling Obesity Policy15
“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 Self15
“An Active, Productive Life”: Narratives of, and Through, Participation in Public and Patient Involvement in Health Research14
Physiotherapists’ Approaches to Patients’ Concerns in Back Pain Consultations Following a Psychologically Informed Training Program14
Unvaxxed: A Cultural Study of the Online Anti-Vaccination Movement14
Sick of the Sick Role: Narratives of What “Recovery” Means to People With CFS/ME14
Caregiver Support in Mental Health Recovery: A Critical Realist Qualitative Research14
“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
Collaborative Filmmaking: A Participatory, Visual Research Method13
Simulation-Based Research: A Scoping Review13
Health Care Providers’ Challenges to High-Quality HIV Care and Antiretroviral Treatment Retention in Rural South Africa13
“What Will Come Will Come”: The Journey of Adjustment and Acceptance on the Path of Dementia Care Among Vietnamese Family Caregivers13
Decisions and Dilemmas: The Context of Prioritization Dilemmas and Influences on Staff Members’ Prioritization Decisions in Residential Aged Care13
Qualitative Data Sharing: Participant Understanding, Motivation, and Consent12
Designing an “Ideal” Substance Use Disorder Treatment Center: Perspectives of People Who Have Utilized Medications for Opioid Use Disorder12
“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
Moving Beyond Text-and-Talk in Qualitative Health Research: Methodological Considerations of Using Multiple Media for Data Collection12
The Social Construction of a Concept—Orthorexia Nervosa: Morality Narratives and Psycho-Politics12
“Now I Am Myself”: Exploring How People With Poststroke Aphasia Experienced Solution-Focused Brief Therapy Within the SOFIA Trial12
“Body as a Machine”: How Adolescents With Sickle Cell Disease Construct Their Fatigue Experiences11
“But I Gathered My Courage”: HIV Self-Testing as a Pathway of Empowerment Among Ugandan Female Sex Workers11
“I Feel Abused by My Own Mind”: Themes of Control in Men’s Online Accounts of Living With Anxiety11
Black Women’s Lived Experiences of Abortion11
The “Sticky Notes” Method: Adapting Interpretive Description Methodology for Team-Based Qualitative Analysis in Community-Based Participatory Research11
Experiences of Pain in Hospitalized Children During Hematopoietic Stem Cell Transplantation Therapy11
“Painful, yet Beautiful, Moments”: Pathways Through Infant Feeding and Dynamic Conceptions of Breastfeeding Success11
The Experts’ Advice: Prevention and Responsibility in German Media and Scientific Discourses on Dementia11
Feelings, Thoughts, and Behaviors During Disaster11
The Other Side of Through: Young Breast Cancer Survivors’ Spectrum of Sexual and Reproductive Health Needs11
Age, Dementia, and Diagnostic Candidacy: Examining the Diagnosis of Young Onset Dementia Using the Candidacy Framework11
Negotiating Female Genital Cutting in a Transnational Context11
We Need to Talk About Complexity in Health Research: Findings From a Focused Ethnography11
Why the Qualitative Health Research (QHR) Review Process Does Not Use Checklists11
Sexual and Reproductive Health Information and Experiences Among Syrian Refugee Adolescent Girls in Lebanon11
The Experiences of People Living With Chronic Pain During a Pandemic: “Crumbling Dreams With Uncertain Futures”11
Co-designing an Integrated Care Network With People Living With Parkinson’s Disease: From Patients’ Narratives to Trajectory Analysis10
Yarning as an Interview Method for Non-Indigenous Clinicians and Health Researchers10
Harm Reduction for Women in Treatment for Alcohol Use Problems: Exploring the Impact of Dominant Addiction Discourse10
How to Save a Life: Vital Clues From Men Who Have Attempted Suicide10
Cancer-Related Decision-Making Among Adolescents, Young Adults, Caregivers, and Oncology Providers10
Qualitative Methods in Health Policy and Systems Research: A Framework for Study Planning10
Parental Perspectives on Family Mealtimes Related to Gastrostomy Tube Feeding in Children10
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 Approach10
Navigating Intersectional Stigma: Strategies for Coping Among Cisgender Women of Color10
“The Drug Use Unfortunately isn’t all Bad”: Chronic Disease Self-Management Complexity and Strategy Among Marginalized People Who Use Drugs10
How do Healthcare Workers ‘Do’ Guidelines? Exploring How Policy Decisions Impacted UK Healthcare Workers During the First Phase of the COVID-19 Pandemic9
The Balance of Patient Involvement: Patients’ and Health Professionals’ Perspectives on Decision-Making in the Treatment of Advanced Prostate Cancer9
Organ Transplant Recipients’ Experiences of Physical Activity: Health, Self-Care, and Transliminality9
Motivations for PrEP-Related Interpersonal Communication Among Women Who Inject Drugs: A Qualitative Egocentric Network Study9
Not Enough Money and Too Many Thoughts: Exploring Perceptions of Mental Health in Two Ugandan Districts Through the Mental Health Literacy Framework9
“We All Join Hands”: Perceptions of the Kangaroo Method Among Female Relatives of Newborns in The Gambia9
“You Are By No Means Alone”: A Netnographic Study of Self-Care Support in an Online Community for Older Adults9
Development of PARcific Approach: Participatory Action Research Methodology for Collectivist Health Research9
(Mis)recognition in the Therapeutic Alliance: The Experience of Mental Health Interpreters Working With Refugees in U.K. Clinical Settings9
Understanding the Lived Experience of Children With Type 1 Diabetes in Kenya: Daily Routines and Adaptation Over Time9
“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 Unit9
Community Perspectives on Social Influences on Suicide Within a Native American Reservation9
The Parental Struggle With the Israeli Genital Socialization Process9
The Changing Narratives of Death, Dying, and HIV in the United Kingdom9
From Danger to Uncertainty: Changing Health Care Practices, Everyday Experiences, and Temporalities in Dealing With COVID-19 Policies in the Netherlands9
Diabetes Identity: A Mechanism of Social Change9
Stumbling Into Adulthood: Learning From Depression While Growing Up9
“Why Would I Talk To Them About Sex?”: Exploring Patient-Provider Communication Among Black Women Experiencing Sexual Pain9
Dignity as an Intersubjective Phenomenon: Experiences of Dyads Living With Serious Illness9
Photovoice Revisited: Dialogue and Action as Pivotal9
‘The System is Not Set up for the Benefit of Women’: Women’s Experiences of Decision-Making During Pregnancy and Birth in Ireland9
Experiences of Tourette Syndrome Caregivers With Supportive Communication8
From Theory to Implementation: Adaptations to a Quality Improvement Initiative According to Implementation Context8
“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
Adherence and the Moral Construction of the Self: A Narrative Analysis of Anticoagulant Medication8
The Impact of Binational Barriers to Medical Care on the Care-Seeking Practices of Mexican Immigrants8
Observation and Institutional Ethnography: Helping Us to See Better8
Cultural Bereavement and Resilience in Refugee Resettlement: A Photovoice Study With Yazidi Women in the Midwest United States8
The “Be All and End All”? Young People, Online Sexual Health Information, Science and Skepticism8
Making Public Involvement in Research More Inclusive of People With Complex Speech and Motor Disorders: The I-ASC Project8
U.S. Abortion Care Providers’ Perspectives on Self-Managed Abortion8
Where Does Value Lie in Peer Support? An Exploratory Discussion of the Theories and Methods Underpinning Effective Research in Peer Support8
Reframing How Early Pregnancy Loss Is Viewed in the Emergency Department8
Chronic Illness Management in Culturally and Linguistically Diverse Patients: Exploring the Needs, Access, and Understanding of Information8
Contributions of Preventive Social Services in Early Childhood Home Visiting in a Disadvantaged Area of Sweden: The Practice of the Parental Advisor8
Living With Fear: Experiences of Danish Parents in Vulnerable Positions During Pregnancy and in the Postnatal Period8
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
Socially Constructing Healthy Eating: A Foucauldian Discourse Analysis of Healthy Eating Information and Advice8
‘Today Was Probably One of the Most Challenging Workdays I’ve Ever Had’: Doing Remote Qualitative Research with Hospital Doctors During the COVID-19 Pandemic8
Surprise Reveals the Affective-Moral Economies in Cancer Illness Narratives8
“Did I Choose a Birth Control Method Yet?”: Health Care and Women’s Contraceptive Decision-Making8
Acceptance of the HPV Vaccine in a Multiethnic Sample of Latinx Mothers8
“What other choices might I have made?”: Sexual Minority Men, the PrEP Cascade and the Shifting Subjective Dimensions of HIV Risk8
Grassroots Mental Health Groups’ Use of Advocacy Strategies in Social Media Messaging8
Modes of Interaction in Naturally Occurring Medical Encounters With General Practitioners: The “One in a Million” Study8
“Sewing Is Part of Our Tradition”: A Case Study of Sewing as a Strategy for Arts-Based Inquiry in Health Research With Inuit Women7
Using Linguistic Ethnography to Study Video Consultations: A Call to Action and Future Research Agenda7
Ethnography in Health Services Research: Oscillation Between Theory and Practice7
Ethics Review Boards for Research With Human Participants: Past, Present, and Future7
Evaluating Complex Interventions Using Qualitative Longitudinal Research: A Case Study of Understanding Pathways to Violence Prevention7
“It’s a Bit of a Double-Edged Sword”: Motivation and Personal Impact of Bereaved Mothers’ Advocacy for Drug Policy Reform7
Understanding the Course of Critical Illness Through a Lifeworld Approach7
Experiencing the SARS-CoV-2 Pandemic Whilst Living With Cancer7
Professional Interpreters and Vicarious Trauma: An Australian Perspective7
Healthcare Barriers Among Working-Age Persons with Disabilities in Trinidad7
‘I Have to Explain to him’: How Companions Broker Mutual Understanding Between Patients with Intellectual Disabilities and Health Care Practitioners in Primary Care7
HIV Diagnosis as Both Biographical Disruption and Biographical Reinforcement: Experiences of HIV Diagnoses Among Recently Diagnosed People Living With HIV7
Using Black Feminist Theory and Methods to Uncover Best Practices in Health Promotion Programming7
Treatment Experiences Among People Who Use Opioids: A Social Ecological Approach7
The Emotional and Psychological Labor of Insider Qualitative Research Among Systemically Marginalized Groups: Revisiting the Uses of Reflexivity7
The (Co)Production of Difference in the Care of Patients With Cancer From Migrant Backgrounds7
Managing Precarity: Understanding Latinas’ Sexual and Reproductive Care-Seeking in a Midwest Emergent Latino Community7
The Challenges of Conducting Qualitative Research on “couples” in Abusive Intimate Partner Relationships Involving Substance Use7
Successfully Negotiating Life Challenges: Learnings From Adults With Cerebral Palsy7
Emerging From the “Ku:” Fluctuating in Adjusting With Breast Cancer—A Post-Traumatic Growth Theory Situated Within Chinese Culture7
Social Processes Informing Toileting Behavior Among Adolescent and Adult Women: Social Cognitive Theory as an Interpretative Lens7
How Culture Shapes Informal Caregiver Motivations: A Meta-Ethnographic Review7
Evaluation of a 20-Month Physical Activity Intervention to Improve Motivational and Affective Outcomes Among Disadvantaged Adult Women7
Comparing Patients’ Experiences in Three Differentiated Service Delivery Models for HIV Treatment in South Africa7
Introducing SAMMSA, a Five-Step Method for Producing ‘Quality’ Qualitative Analysis7
Emotional Health Work of Women With Female Genital Cutting Prior to Reproductive Health Care Encounters7
“What I Would Do to Take Away Your Pain”: A Photovoice Project Conducted by Mothers of Children With Medical Complexity7
Perspectives and Experiences of Obstetricians Who Provide Labor and Delivery Care for Micronesian Women in Hawai‘i: What Is Driving Cesarean Delivery Rates?7
Identifying and Responding to Delirium in Acute Stroke: Clinical Team Members’ Understandings7
Dialoguing With Images: An Expressive Arts Method for Health Research7
A Life Course Perspective on Growing Older With Cerebral Palsy7
Trans Youth Talk Back: A Foucauldian Discourse Analysis of Transgender Minors’ Accounts of Healthcare Access7
Exploration of Physical Activity Barriers and Facilitators Among Adults in Kathmandu, Nepal7
Exploring Indigenous Ways of Coping After a Wildfire Disaster in Northern Alberta, Canada7
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